Item | Value |
---|---|
geneid | 27253 |
ensemblid | ENSG00000118946.12 |
hgncid | 14267 |
symbol | PCDH17 |
name | protocadherin 17 |
refseq_nuc | NM_001040429.3 |
refseq_prot | NP_001035519.1 |
ensembl_nuc | ENST00000377918.8 |
ensembl_prot | ENSP00000367151.3 |
mane_status | MANE Select |
chr | chr13 |
start | 57631744 |
end | 57729311 |
strand | + |
ver | v1.2 |
region | chr13:57631744-57729311 |
region5000 | chr13:57626744-57734311 |
regionname0 | PCDH17_chr13_57631744_57729311 |
regionname5000 | PCDH17_chr13_57626744_57734311 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 1159 | 303 | 70 | 67 | 128 | 11 | 25 | 102 | PCDH17_chr13_57626744_57734311 | PCDH17 | copy fasta | chr13 | 57626744 | 57734311 |
a0002 | 0/0 | 1159 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PCDH17_chr13_57626744_57734311 | PCDH17 | copy fasta | chr13 | 57626744 | 57734311 |
a0003 | 0/0 | 1159 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PCDH17_chr13_57626744_57734311 | PCDH17 | copy fasta | chr13 | 57626744 | 57734311 |
a0004 | 0/0 | 1159 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | copy fasta | chr13 | 57626744 | 57734311 |
a0005 | 0/0 | 1159 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | copy fasta | chr13 | 57626744 | 57734311 |
a0006 | 0/0 | 1159 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PCDH17_chr13_57626744_57734311 | PCDH17 | copy fasta | chr13 | 57626744 | 57734311 |
a0007 | 0/0 | 1159 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PCDH17_chr13_57626744_57734311 | PCDH17 | copy fasta | chr13 | 57626744 | 57734311 |
a0008 | 0/0 | 1159 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | copy fasta | chr13 | 57626744 | 57734311 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 3480 | 287 | 63 | 66 | 122 | 10 | 24 | PCDH17_chr13_57626744_57734311 | PCDH17 | copy fasta | chr13 | 57626744 | 57734311 |
c0002 | 0/0 | 3480 | 4 | 4 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | copy fasta | chr13 | 57626744 | 57734311 |
c0003 | 0/0 | 3480 | 3 | 0 | 0 | 2 | 1 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | copy fasta | chr13 | 57626744 | 57734311 |
c0004 | 0/0 | 3480 | 2 | 2 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | copy fasta | chr13 | 57626744 | 57734311 |
c0005 | 0/0 | 3480 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | copy fasta | chr13 | 57626744 | 57734311 |
c0006 | 0/0 | 3480 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | copy fasta | chr13 | 57626744 | 57734311 |
c0007 | 0/0 | 3480 | 1 | 0 | 0 | 0 | 0 | 1 | PCDH17_chr13_57626744_57734311 | PCDH17 | copy fasta | chr13 | 57626744 | 57734311 |
c0008 | 0/0 | 3480 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | copy fasta | chr13 | 57626744 | 57734311 |
c0009 | 0/0 | 3480 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | copy fasta | chr13 | 57626744 | 57734311 |
c0010 | 0/0 | 3480 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | copy fasta | chr13 | 57626744 | 57734311 |
c0011 | 0/0 | 3480 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | copy fasta | chr13 | 57626744 | 57734311 |
c0012 | 0/0 | 3480 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | copy fasta | chr13 | 57626744 | 57734311 |
c0013 | 0/0 | 3480 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | copy fasta | chr13 | 57626744 | 57734311 |
c0014 | 0/0 | 3480 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | copy fasta | chr13 | 57626744 | 57734311 |
c0015 | 0/0 | 3480 | 1 | 0 | 0 | 0 | 1 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | copy fasta | chr13 | 57626744 | 57734311 |
c0016 | 0/0 | 3480 | 1 | 0 | 0 | 0 | 0 | 1 | PCDH17_chr13_57626744_57734311 | PCDH17 | copy fasta | chr13 | 57626744 | 57734311 |
c0017 | 0/0 | 3480 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | copy fasta | chr13 | 57626744 | 57734311 |
c0018 | 0/0 | 3480 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | copy fasta | chr13 | 57626744 | 57734311 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 4818 | 55 | 6 | 15 | 24 | 2 | 8 | PCDH17_chr13_57626744_57734311 | PCDH17 | copy fasta | chr13 | 57626744 | 57734311 |
t0002 | 0/0 | 4821 | 53 | 23 | 7 | 19 | 2 | 2 | PCDH17_chr13_57626744_57734311 | PCDH17 | copy fasta | chr13 | 57626744 | 57734311 |
t0003 | 0/0 | 4820 | 33 | 1 | 19 | 7 | 2 | 4 | PCDH17_chr13_57626744_57734311 | PCDH17 | copy fasta | chr13 | 57626744 | 57734311 |
t0004 | 0/0 | 4819 | 20 | 4 | 5 | 9 | 1 | 1 | PCDH17_chr13_57626744_57734311 | PCDH17 | copy fasta | chr13 | 57626744 | 57734311 |
t0005 | 0/0 | 4820 | 17 | 13 | 1 | 2 | 0 | 1 | PCDH17_chr13_57626744_57734311 | PCDH17 | copy fasta | chr13 | 57626744 | 57734311 |
t0006 | 0/1 | 4819 | 16 | 2 | 5 | 5 | 1 | 2 | PCDH17_chr13_57626744_57734311 | PCDH17 | copy fasta | chr13 | 57626744 | 57734311 |
t0007 | 0/0 | 4819 | 13 | 0 | 0 | 11 | 1 | 1 | PCDH17_chr13_57626744_57734311 | PCDH17 | copy fasta | chr13 | 57626744 | 57734311 |
t0008 | 0/0 | 4821 | 12 | 1 | 3 | 7 | 1 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | copy fasta | chr13 | 57626744 | 57734311 |
t0009 | 0/0 | 4822 | 10 | 0 | 5 | 2 | 1 | 2 | PCDH17_chr13_57626744_57734311 | PCDH17 | copy fasta | chr13 | 57626744 | 57734311 |
t0010 | 0/0 | 4819 | 8 | 2 | 2 | 3 | 0 | 1 | PCDH17_chr13_57626744_57734311 | PCDH17 | copy fasta | chr13 | 57626744 | 57734311 |
t0011 | 0/0 | 4819 | 7 | 0 | 0 | 7 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | copy fasta | chr13 | 57626744 | 57734311 |
t0012 | 0/0 | 4820 | 5 | 0 | 0 | 5 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | copy fasta | chr13 | 57626744 | 57734311 |
t0013 | 0/0 | 4820 | 4 | 1 | 0 | 1 | 0 | 2 | PCDH17_chr13_57626744_57734311 | PCDH17 | copy fasta | chr13 | 57626744 | 57734311 |
t0014 | 0/0 | 4819 | 4 | 0 | 0 | 4 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | copy fasta | chr13 | 57626744 | 57734311 |
t0015 | 0/0 | 4818 | 3 | 3 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | copy fasta | chr13 | 57626744 | 57734311 |
t0016 | 0/0 | 4818 | 3 | 0 | 0 | 3 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | copy fasta | chr13 | 57626744 | 57734311 |
t0017 | 0/0 | 4820 | 2 | 0 | 0 | 2 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | copy fasta | chr13 | 57626744 | 57734311 |
t0018 | 0/0 | 4821 | 2 | 2 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | copy fasta | chr13 | 57626744 | 57734311 |
t0019 | 0/0 | 4820 | 2 | 0 | 0 | 2 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | copy fasta | chr13 | 57626744 | 57734311 |
t0020 | 0/0 | 4822 | 2 | 0 | 2 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | copy fasta | chr13 | 57626744 | 57734311 |
t0021 | 0/0 | 4820 | 2 | 0 | 1 | 0 | 0 | 1 | PCDH17_chr13_57626744_57734311 | PCDH17 | copy fasta | chr13 | 57626744 | 57734311 |
t0022 | 0/0 | 4820 | 2 | 1 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | copy fasta | chr13 | 57626744 | 57734311 |
t0023 | 0/0 | 4819 | 2 | 0 | 0 | 2 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | copy fasta | chr13 | 57626744 | 57734311 |
t0024 | 0/0 | 4819 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | copy fasta | chr13 | 57626744 | 57734311 |
t0025 | 0/0 | 4818 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | copy fasta | chr13 | 57626744 | 57734311 |
t0026 | 0/0 | 4820 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | copy fasta | chr13 | 57626744 | 57734311 |
t0027 | 0/0 | 4821 | 1 | 0 | 0 | 0 | 1 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | copy fasta | chr13 | 57626744 | 57734311 |
t0028 | 0/0 | 4819 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | copy fasta | chr13 | 57626744 | 57734311 |
t0029 | 0/0 | 4819 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | copy fasta | chr13 | 57626744 | 57734311 |
t0030 | 0/0 | 4822 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | copy fasta | chr13 | 57626744 | 57734311 |
t0031 | 0/0 | 4821 | 1 | 0 | 0 | 0 | 0 | 1 | PCDH17_chr13_57626744_57734311 | PCDH17 | copy fasta | chr13 | 57626744 | 57734311 |
t0032 | 1/0 | 4821 | 1 | 0 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | copy fasta | chr13 | 57626744 | 57734311 |
t0033 | 0/0 | 4822 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | copy fasta | chr13 | 57626744 | 57734311 |
t0034 | 0/0 | 4820 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | copy fasta | chr13 | 57626744 | 57734311 |
t0035 | 0/0 | 4821 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | copy fasta | chr13 | 57626744 | 57734311 |
t0036 | 0/0 | 4819 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | copy fasta | chr13 | 57626744 | 57734311 |
t0037 | 0/0 | 4821 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | copy fasta | chr13 | 57626744 | 57734311 |
t0038 | 0/0 | 4821 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | copy fasta | chr13 | 57626744 | 57734311 |
t0039 | 0/0 | 4822 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | copy fasta | chr13 | 57626744 | 57734311 |
t0040 | 0/0 | 4822 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | copy fasta | chr13 | 57626744 | 57734311 |
t0041 | 0/0 | 4821 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | copy fasta | chr13 | 57626744 | 57734311 |
t0042 | 0/0 | 4819 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | copy fasta | chr13 | 57626744 | 57734311 |
t0043 | 0/0 | 4822 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | copy fasta | chr13 | 57626744 | 57734311 |
t0044 | 0/0 | 4819 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | copy fasta | chr13 | 57626744 | 57734311 |
t0045 | 0/0 | 4819 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | copy fasta | chr13 | 57626744 | 57734311 |
t0046 | 0/0 | 4822 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | copy fasta | chr13 | 57626744 | 57734311 |
t0047 | 0/0 | 4820 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | copy fasta | chr13 | 57626744 | 57734311 |
t0048 | 0/0 | 4819 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | copy fasta | chr13 | 57626744 | 57734311 |
t0049 | 0/0 | 4818 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | copy fasta | chr13 | 57626744 | 57734311 |
t0050 | 0/0 | 4820 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | copy fasta | chr13 | 57626744 | 57734311 |
t0051 | 0/0 | 4821 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | copy fasta | chr13 | 57626744 | 57734311 |
t0052 | 0/0 | 4819 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | copy fasta | chr13 | 57626744 | 57734311 |
t0053 | 0/0 | 4818 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | copy fasta | chr13 | 57626744 | 57734311 |
t0054 | 0/0 | 4820 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | copy fasta | chr13 | 57626744 | 57734311 |
t0055 | 0/0 | 4819 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | copy fasta | chr13 | 57626744 | 57734311 |
t0056 | 0/0 | 4819 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | copy fasta | chr13 | 57626744 | 57734311 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0024 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0028 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0029 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0030 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0032 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0105 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0216 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0235 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0242 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0294 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 3480 | 287 | 63 | 66 | 122 | 10 | 24 | PCDH17_chr13_57626744_57734311 | PCDH17 | copy fasta | chr13 | 57626744 | 57734311 |
a0001c0002 | 0/0 | 3480 | 4 | 4 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | copy fasta | chr13 | 57626744 | 57734311 |
a0001c0003 | 0/0 | 3480 | 3 | 0 | 0 | 2 | 1 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | copy fasta | chr13 | 57626744 | 57734311 |
a0001c0004 | 0/0 | 3480 | 2 | 2 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | copy fasta | chr13 | 57626744 | 57734311 |
a0001c0005 | 0/0 | 3480 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | copy fasta | chr13 | 57626744 | 57734311 |
a0001c0006 | 0/0 | 3480 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | copy fasta | chr13 | 57626744 | 57734311 |
a0001c0010 | 0/0 | 3480 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | copy fasta | chr13 | 57626744 | 57734311 |
a0001c0011 | 0/0 | 3480 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | copy fasta | chr13 | 57626744 | 57734311 |
a0001c0012 | 0/0 | 3480 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | copy fasta | chr13 | 57626744 | 57734311 |
a0001c0013 | 0/0 | 3480 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | copy fasta | chr13 | 57626744 | 57734311 |
a0001c0016 | 0/0 | 3480 | 1 | 0 | 0 | 0 | 0 | 1 | PCDH17_chr13_57626744_57734311 | PCDH17 | copy fasta | chr13 | 57626744 | 57734311 |
a0002c0018 | 0/0 | 3480 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | copy fasta | chr13 | 57626744 | 57734311 |
a0003c0017 | 0/0 | 3480 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | copy fasta | chr13 | 57626744 | 57734311 |
a0004c0015 | 0/0 | 3480 | 1 | 0 | 0 | 0 | 1 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | copy fasta | chr13 | 57626744 | 57734311 |
a0005c0014 | 0/0 | 3480 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | copy fasta | chr13 | 57626744 | 57734311 |
a0006c0009 | 0/0 | 3480 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | copy fasta | chr13 | 57626744 | 57734311 |
a0007c0008 | 0/0 | 3480 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | copy fasta | chr13 | 57626744 | 57734311 |
a0008c0007 | 0/0 | 3480 | 1 | 0 | 0 | 0 | 0 | 1 | PCDH17_chr13_57626744_57734311 | PCDH17 | copy fasta | chr13 | 57626744 | 57734311 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 8297 | 50 | 4 | 15 | 22 | 1 | 8 | PCDH17_chr13_57626744_57734311 | PCDH17 | copy fasta | chr13 | 57626744 | 57734311 |
a0001c0001t0002 | 0/0 | 8300 | 51 | 23 | 7 | 17 | 2 | 2 | PCDH17_chr13_57626744_57734311 | PCDH17 | copy fasta | chr13 | 57626744 | 57734311 |
a0001c0001t0003 | 0/0 | 8299 | 31 | 1 | 18 | 7 | 1 | 4 | PCDH17_chr13_57626744_57734311 | PCDH17 | copy fasta | chr13 | 57626744 | 57734311 |
a0001c0001t0004 | 0/0 | 8298 | 20 | 4 | 5 | 9 | 1 | 1 | PCDH17_chr13_57626744_57734311 | PCDH17 | copy fasta | chr13 | 57626744 | 57734311 |
a0001c0001t0005 | 0/0 | 8299 | 13 | 10 | 1 | 2 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | copy fasta | chr13 | 57626744 | 57734311 |
a0001c0001t0006 | 0/1 | 8298 | 13 | 1 | 4 | 5 | 1 | 1 | PCDH17_chr13_57626744_57734311 | PCDH17 | copy fasta | chr13 | 57626744 | 57734311 |
a0001c0001t0007 | 0/0 | 8298 | 12 | 0 | 0 | 10 | 1 | 1 | PCDH17_chr13_57626744_57734311 | PCDH17 | copy fasta | chr13 | 57626744 | 57734311 |
a0001c0001t0008 | 0/0 | 8300 | 12 | 1 | 3 | 7 | 1 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | copy fasta | chr13 | 57626744 | 57734311 |
a0001c0001t0009 | 0/0 | 8301 | 10 | 0 | 5 | 2 | 1 | 2 | PCDH17_chr13_57626744_57734311 | PCDH17 | copy fasta | chr13 | 57626744 | 57734311 |
a0001c0001t0010 | 0/0 | 8298 | 8 | 2 | 2 | 3 | 0 | 1 | PCDH17_chr13_57626744_57734311 | PCDH17 | copy fasta | chr13 | 57626744 | 57734311 |
a0001c0001t0011 | 0/0 | 8298 | 5 | 0 | 0 | 5 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | copy fasta | chr13 | 57626744 | 57734311 |
a0001c0001t0012 | 0/0 | 8299 | 5 | 0 | 0 | 5 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | copy fasta | chr13 | 57626744 | 57734311 |
a0001c0001t0013 | 0/0 | 8299 | 4 | 1 | 0 | 1 | 0 | 2 | PCDH17_chr13_57626744_57734311 | PCDH17 | copy fasta | chr13 | 57626744 | 57734311 |
a0001c0001t0014 | 0/0 | 8298 | 4 | 0 | 0 | 4 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | copy fasta | chr13 | 57626744 | 57734311 |
a0001c0001t0015 | 0/0 | 8297 | 3 | 3 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | copy fasta | chr13 | 57626744 | 57734311 |
a0001c0001t0016 | 0/0 | 8297 | 2 | 0 | 0 | 2 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | copy fasta | chr13 | 57626744 | 57734311 |
a0001c0001t0017 | 0/0 | 8299 | 2 | 0 | 0 | 2 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | copy fasta | chr13 | 57626744 | 57734311 |
a0001c0001t0018 | 0/0 | 8300 | 2 | 2 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | copy fasta | chr13 | 57626744 | 57734311 |
a0001c0001t0019 | 0/0 | 8299 | 2 | 0 | 0 | 2 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | copy fasta | chr13 | 57626744 | 57734311 |
a0001c0001t0020 | 0/0 | 8301 | 2 | 0 | 2 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | copy fasta | chr13 | 57626744 | 57734311 |
a0001c0001t0021 | 0/0 | 8299 | 2 | 0 | 1 | 0 | 0 | 1 | PCDH17_chr13_57626744_57734311 | PCDH17 | copy fasta | chr13 | 57626744 | 57734311 |
a0001c0001t0022 | 0/0 | 8299 | 2 | 1 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | copy fasta | chr13 | 57626744 | 57734311 |
a0001c0001t0023 | 0/0 | 8298 | 2 | 0 | 0 | 2 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | copy fasta | chr13 | 57626744 | 57734311 |
a0001c0001t0024 | 0/0 | 8298 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | copy fasta | chr13 | 57626744 | 57734311 |
a0001c0001t0025 | 0/0 | 8297 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | copy fasta | chr13 | 57626744 | 57734311 |
a0001c0001t0026 | 0/0 | 8299 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | copy fasta | chr13 | 57626744 | 57734311 |
a0001c0001t0027 | 0/0 | 8300 | 1 | 0 | 0 | 0 | 1 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | copy fasta | chr13 | 57626744 | 57734311 |
a0001c0001t0029 | 0/0 | 8298 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | copy fasta | chr13 | 57626744 | 57734311 |
a0001c0001t0030 | 0/0 | 8301 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | copy fasta | chr13 | 57626744 | 57734311 |
a0001c0001t0031 | 0/0 | 8300 | 1 | 0 | 0 | 0 | 0 | 1 | PCDH17_chr13_57626744_57734311 | PCDH17 | copy fasta | chr13 | 57626744 | 57734311 |
a0001c0001t0032 | 1/0 | 8300 | 1 | 0 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | copy fasta | chr13 | 57626744 | 57734311 |
a0001c0001t0033 | 0/0 | 8301 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | copy fasta | chr13 | 57626744 | 57734311 |
a0001c0001t0034 | 0/0 | 8299 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | copy fasta | chr13 | 57626744 | 57734311 |
a0001c0001t0035 | 0/0 | 8300 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | copy fasta | chr13 | 57626744 | 57734311 |
a0001c0001t0036 | 0/0 | 8298 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | copy fasta | chr13 | 57626744 | 57734311 |
a0001c0001t0037 | 0/0 | 8300 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | copy fasta | chr13 | 57626744 | 57734311 |
a0001c0001t0038 | 0/0 | 8300 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | copy fasta | chr13 | 57626744 | 57734311 |
a0001c0001t0039 | 0/0 | 8301 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | copy fasta | chr13 | 57626744 | 57734311 |
a0001c0001t0040 | 0/0 | 8301 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | copy fasta | chr13 | 57626744 | 57734311 |
a0001c0001t0041 | 0/0 | 8300 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | copy fasta | chr13 | 57626744 | 57734311 |
a0001c0001t0042 | 0/0 | 8298 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | copy fasta | chr13 | 57626744 | 57734311 |
a0001c0001t0043 | 0/0 | 8301 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | copy fasta | chr13 | 57626744 | 57734311 |
a0001c0001t0044 | 0/0 | 8298 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | copy fasta | chr13 | 57626744 | 57734311 |
a0001c0001t0046 | 0/0 | 8301 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | copy fasta | chr13 | 57626744 | 57734311 |
a0001c0001t0047 | 0/0 | 8299 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | copy fasta | chr13 | 57626744 | 57734311 |
a0001c0001t0048 | 0/0 | 8298 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | copy fasta | chr13 | 57626744 | 57734311 |
a0001c0001t0050 | 0/0 | 8299 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | copy fasta | chr13 | 57626744 | 57734311 |
a0001c0001t0051 | 0/0 | 8300 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | copy fasta | chr13 | 57626744 | 57734311 |
a0001c0001t0052 | 0/0 | 8298 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | copy fasta | chr13 | 57626744 | 57734311 |
a0001c0001t0053 | 0/0 | 8297 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | copy fasta | chr13 | 57626744 | 57734311 |
a0001c0001t0054 | 0/0 | 8299 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | copy fasta | chr13 | 57626744 | 57734311 |
a0001c0001t0055 | 0/0 | 8298 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | copy fasta | chr13 | 57626744 | 57734311 |
a0001c0001t0056 | 0/0 | 8298 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | copy fasta | chr13 | 57626744 | 57734311 |
a0001c0002t0001 | 0/0 | 8297 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | copy fasta | chr13 | 57626744 | 57734311 |
a0001c0002t0005 | 0/0 | 8299 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | copy fasta | chr13 | 57626744 | 57734311 |
a0001c0002t0006 | 0/0 | 8298 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | copy fasta | chr13 | 57626744 | 57734311 |
a0001c0002t0049 | 0/0 | 8297 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | copy fasta | chr13 | 57626744 | 57734311 |
a0001c0003t0001 | 0/0 | 8297 | 1 | 0 | 0 | 0 | 1 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | copy fasta | chr13 | 57626744 | 57734311 |
a0001c0003t0002 | 0/0 | 8300 | 2 | 0 | 0 | 2 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | copy fasta | chr13 | 57626744 | 57734311 |
a0001c0004t0005 | 0/0 | 8299 | 2 | 2 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | copy fasta | chr13 | 57626744 | 57734311 |
a0001c0005t0028 | 0/0 | 8298 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | copy fasta | chr13 | 57626744 | 57734311 |
a0001c0006t0003 | 0/0 | 8299 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | copy fasta | chr13 | 57626744 | 57734311 |
a0001c0010t0001 | 0/0 | 8297 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | copy fasta | chr13 | 57626744 | 57734311 |
a0001c0011t0001 | 0/0 | 8297 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | copy fasta | chr13 | 57626744 | 57734311 |
a0001c0012t0001 | 0/0 | 8297 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | copy fasta | chr13 | 57626744 | 57734311 |
a0001c0013t0016 | 0/0 | 8297 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | copy fasta | chr13 | 57626744 | 57734311 |
a0001c0016t0005 | 0/0 | 8299 | 1 | 0 | 0 | 0 | 0 | 1 | PCDH17_chr13_57626744_57734311 | PCDH17 | copy fasta | chr13 | 57626744 | 57734311 |
a0002c0018t0011 | 0/0 | 8298 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | copy fasta | chr13 | 57626744 | 57734311 |
a0003c0017t0011 | 0/0 | 8298 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | copy fasta | chr13 | 57626744 | 57734311 |
a0004c0015t0003 | 0/0 | 8299 | 1 | 0 | 0 | 0 | 1 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | copy fasta | chr13 | 57626744 | 57734311 |
a0005c0014t0006 | 0/0 | 8298 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | copy fasta | chr13 | 57626744 | 57734311 |
a0006c0009t0007 | 0/0 | 8298 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | copy fasta | chr13 | 57626744 | 57734311 |
a0007c0008t0045 | 0/0 | 8298 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | copy fasta | chr13 | 57626744 | 57734311 |
a0008c0007t0006 | 0/0 | 8298 | 1 | 0 | 0 | 0 | 0 | 1 | PCDH17_chr13_57626744_57734311 | PCDH17 | copy fasta | chr13 | 57626744 | 57734311 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0001g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0001g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0001g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0002g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0002g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0002g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0002g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0002g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0002g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0002g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0002g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0002g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0002g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0002g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0002g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0002g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0002g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0002g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0002g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0002g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0002g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0002g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0002g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0002g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0002g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0002g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0002g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0002g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0002g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0002g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0002g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0002g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0002g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0003g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0003g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0003g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0003g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0003g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0003g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0003g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0003g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0003g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0003g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0003g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0003g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0003g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0003g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0003g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0003g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0003g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0003g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0003g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0003g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0003g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0003g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0003g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0003g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0003g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0003g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0003g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0003g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0003g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0003g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0003g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0004g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0004g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0004g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0004g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0004g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0004g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0004g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0004g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0004g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0004g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0004g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0004g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0004g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0004g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0004g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0004g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0004g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0004g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0004g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0005g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0005g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0005g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0005g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0005g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0005g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0005g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0005g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0005g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0005g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0005g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0005g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0005g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0006g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0006g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0006g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0006g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0006g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0006g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0006g0105 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0006g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0006g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0006g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0006g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0006g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0006g0242 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0007g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0007g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0007g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0007g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0007g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0007g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0007g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0007g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0007g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0007g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0007g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0007g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0008g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0008g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0008g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0008g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0008g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0008g0024 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0008g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0008g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0008g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0008g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0008g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0009g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0009g0029 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0009g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0009g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0009g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0009g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0009g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0009g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0009g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0009g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0010g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0010g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0010g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0010g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0010g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0010g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0010g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0010g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0011g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0011g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0011g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0011g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0011g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0012g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0012g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0012g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0012g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0012g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0013g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0013g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0013g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0013g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0014g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0014g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0014g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0015g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0015g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0015g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0016g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0016g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0017g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0017g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0018g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0018g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0019g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0019g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0020g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0020g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0021g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0021g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0022g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0022g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0023g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0023g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0024g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0025g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0026g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0027g0030 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0029g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0030g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0031g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0032g0028 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0033g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0034g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0035g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0036g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0037g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0038g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0039g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0040g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0041g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0042g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0043g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0044g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0046g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0047g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0048g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0050g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0051g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0052g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0053g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0054g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0055g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0001t0056g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0002t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0002t0005g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0002t0006g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0002t0049g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0003t0001g0294 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0003t0002g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0003t0002g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0004t0005g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0004t0005g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0005t0028g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0006t0003g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0010t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0011t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0012t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0013t0016g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0001c0016t0005g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0002c0018t0011g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0003c0017t0011g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0004c0015t0003g0032 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0005c0014t0006g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0006c0009t0007g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0007c0008t0045g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
a0008c0007t0006g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0001 | t0001 | g0167 | EUR | GBR | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
HG00140 | hp2 | a0001 | c0001 | t0006 | g0242 | EUR | GBR | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
HG00280 | hp1 | a0001 | c0003 | t0001 | g0294 | EUR | FIN | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
HG00280 | hp2 | a0004 | c0015 | t0003 | g0032 | EUR | FIN | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
HG00323 | hp1 | a0001 | c0001 | t0007 | g0116 | EUR | FIN | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
HG00323 | hp2 | a0001 | c0001 | t0003 | g0220 | EUR | FIN | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
HG00544 | hp1 | a0001 | c0001 | t0002 | g0256 | EAS | CHS | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
HG00544 | hp2 | a0001 | c0001 | t0033 | g0229 | EAS | CHS | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
HG00558 | hp1 | a0001 | c0001 | t0007 | g0187 | EAS | CHS | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
HG00558 | hp2 | a0001 | c0001 | t0011 | g0182 | EAS | CHS | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
HG00597 | hp1 | a0001 | c0001 | t0002 | g0251 | EAS | CHS | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
HG00597 | hp2 | a0001 | c0001 | t0017 | g0152 | EAS | CHS | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
HG00621 | hp1 | a0001 | c0001 | t0003 | g0253 | EAS | CHS | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
HG00621 | hp2 | a0001 | c0003 | t0002 | g0287 | EAS | CHS | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
HG00639 | hp1 | a0001 | c0001 | t0022 | g0207 | AMR | PUR | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0065 | AMR | PUR | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
HG00673 | hp1 | a0001 | c0001 | t0029 | g0051 | EAS | CHS | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
HG00673 | hp2 | a0001 | c0001 | t0007 | g0173 | EAS | CHS | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0161 | AMR | PUR | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
HG00735 | hp2 | a0001 | c0001 | t0009 | g0034 | AMR | PUR | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
HG00738 | hp1 | a0001 | c0001 | t0003 | g0165 | AMR | PUR | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0186 | AMR | PUR | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
HG00741 | hp1 | a0001 | c0001 | t0010 | g0228 | AMR | PUR | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
HG00741 | hp2 | a0001 | c0001 | t0002 | g0005 | AMR | PUR | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
HG01069 | hp1 | a0001 | c0001 | t0009 | g0037 | AMR | PUR | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
HG01069 | hp2 | a0005 | c0014 | t0006 | g0160 | AMR | PUR | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
HG01074 | hp1 | a0001 | c0001 | t0002 | g0250 | AMR | PUR | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0213 | AMR | PUR | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
HG01081 | hp1 | a0001 | c0001 | t0054 | g0174 | AMR | PUR | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
HG01081 | hp2 | a0001 | c0001 | t0020 | g0108 | AMR | PUR | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
HG01099 | hp1 | a0001 | c0001 | t0003 | g0164 | AMR | PUR | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
HG01099 | hp2 | a0001 | c0006 | t0003 | g0114 | AMR | PUR | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
HG01106 | hp1 | a0001 | c0001 | t0002 | g0068 | AMR | PUR | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
HG01106 | hp2 | a0001 | c0001 | t0006 | g0125 | AMR | PUR | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
HG01109 | hp1 | a0001 | c0001 | t0002 | g0086 | AMR | PUR | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
HG01109 | hp2 | a0001 | c0001 | t0039 | g0267 | AMR | PUR | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
HG01168 | hp1 | a0001 | c0001 | t0021 | g0183 | AMR | PUR | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
HG01168 | hp2 | a0001 | c0001 | t0003 | g0263 | AMR | PUR | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
HG01169 | hp1 | a0001 | c0001 | t0003 | g0045 | AMR | PUR | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
HG01169 | hp2 | a0001 | c0001 | t0003 | g0262 | AMR | PUR | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0170 | AMR | PUR | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
HG01175 | hp2 | a0001 | c0001 | t0006 | g0227 | AMR | PUR | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
HG01192 | hp1 | a0001 | c0001 | t0009 | g0302 | AMR | PUR | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
HG01192 | hp2 | a0001 | c0001 | t0002 | g0005 | AMR | PUR | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
HG01243 | hp1 | a0001 | c0001 | t0004 | g0143 | AMR | PUR | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
HG01243 | hp2 | a0001 | c0001 | t0002 | g0266 | AMR | PUR | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
HG01255 | hp1 | a0001 | c0001 | t0010 | g0090 | AMR | CLM | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
HG01255 | hp2 | a0001 | c0001 | t0009 | g0054 | AMR | CLM | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
HG01256 | hp1 | a0001 | c0001 | t0004 | g0003 | AMR | CLM | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
HG01256 | hp2 | a0001 | c0001 | t0003 | g0070 | AMR | CLM | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
HG01257 | hp1 | a0001 | c0001 | t0008 | g0019 | AMR | CLM | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0110 | AMR | CLM | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
HG01258 | hp1 | a0001 | c0001 | t0008 | g0026 | AMR | CLM | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
HG01258 | hp2 | a0001 | c0001 | t0004 | g0003 | AMR | CLM | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
HG01261 | hp1 | a0001 | c0001 | t0003 | g0217 | AMR | CLM | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
HG01261 | hp2 | a0001 | c0001 | t0009 | g0025 | AMR | CLM | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0158 | AMR | CLM | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
HG01346 | hp2 | a0001 | c0001 | t0020 | g0249 | AMR | CLM | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
HG01361 | hp2 | a0001 | c0001 | t0003 | g0268 | AMR | CLM | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
HG01433 | hp1 | a0001 | c0001 | t0002 | g0223 | AMR | CLM | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0159 | AMR | CLM | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
HG01496 | hp1 | a0001 | c0001 | t0005 | g0275 | AMR | CLM | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0049 | AMR | CLM | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
HG01515 | hp1 | a0001 | c0001 | t0002 | g0216 | EUR | IBS | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
HG01515 | hp2 | a0001 | c0001 | t0027 | g0030 | EUR | IBS | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
HG01884 | hp1 | a0001 | c0001 | t0002 | g0234 | AFR | ACB | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
HG01884 | hp2 | a0001 | c0001 | t0004 | g0148 | AFR | ACB | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
HG01891 | hp1 | a0001 | c0001 | t0002 | g0135 | AFR | ACB | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
HG01891 | hp2 | a0001 | c0001 | t0004 | g0092 | AFR | ACB | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
HG01934 | hp1 | a0001 | c0001 | t0003 | g0041 | AMR | PEL | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
HG01934 | hp2 | a0001 | c0001 | t0003 | g0151 | AMR | PEL | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
HG01943 | hp1 | a0001 | c0001 | t0003 | g0072 | AMR | PEL | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0129 | AMR | PEL | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
HG01952 | hp1 | a0001 | c0001 | t0003 | g0064 | AMR | PEL | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0192 | AMR | PEL | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
HG01975 | hp1 | a0001 | c0001 | t0003 | g0073 | AMR | PEL | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
HG01975 | hp2 | a0001 | c0001 | t0004 | g0137 | AMR | PEL | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
HG01978 | hp1 | a0001 | c0001 | t0003 | g0071 | AMR | PEL | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
HG01978 | hp2 | a0001 | c0001 | t0006 | g0168 | AMR | PEL | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
HG01981 | hp1 | a0001 | c0001 | t0003 | g0188 | AMR | PEL | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
HG01981 | hp2 | a0001 | c0001 | t0006 | g0212 | AMR | PEL | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
HG01993 | hp1 | a0001 | c0001 | t0004 | g0243 | AMR | PEL | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0191 | AMR | PEL | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
HG02015 | hp1 | a0001 | c0001 | t0007 | g0194 | EAS | KHV | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
HG02015 | hp2 | a0001 | c0001 | t0011 | g0047 | EAS | KHV | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
HG02027 | hp1 | a0001 | c0001 | t0008 | g0042 | EAS | KHV | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
HG02027 | hp2 | a0001 | c0001 | t0005 | g0239 | EAS | KHV | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
HG02055 | hp1 | a0001 | c0001 | t0002 | g0236 | AFR | ACB | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
HG02055 | hp2 | a0001 | c0001 | t0018 | g0060 | AFR | ACB | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
HG02074 | hp1 | a0001 | c0001 | t0016 | g0286 | EAS | KHV | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
HG02074 | hp2 | a0001 | c0001 | t0007 | g0172 | EAS | KHV | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
HG02080 | hp1 | a0001 | c0001 | t0016 | g0265 | EAS | KHV | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
HG02080 | hp2 | a0001 | c0001 | t0007 | g0078 | EAS | KHV | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
HG02083 | hp1 | a0001 | c0005 | t0028 | g0052 | EAS | KHV | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
HG02083 | hp2 | a0001 | c0001 | t0004 | g0264 | EAS | KHV | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
HG02129 | hp1 | a0001 | c0001 | t0023 | g0176 | EAS | KHV | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
HG02129 | hp2 | a0001 | c0001 | t0004 | g0117 | EAS | KHV | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
HG02132 | hp1 | a0001 | c0001 | t0007 | g0285 | EAS | KHV | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
HG02132 | hp2 | a0001 | c0001 | t0008 | g0023 | EAS | KHV | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | KHV | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
HG02135 | hp2 | a0001 | c0001 | t0004 | g0215 | EAS | KHV | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0232 | AMR | PEL | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
HG02148 | hp2 | a0001 | c0001 | t0008 | g0017 | AMR | PEL | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
HG02257 | hp1 | a0001 | c0004 | t0005 | g0061 | AFR | ACB | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
HG02257 | hp2 | a0001 | c0001 | t0034 | g0247 | AFR | ACB | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
HG02258 | hp1 | a0001 | c0004 | t0005 | g0062 | AFR | ACB | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0059 | AFR | ACB | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
HG02280 | hp1 | a0001 | c0001 | t0002 | g0102 | AFR | ACB | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
HG02280 | hp2 | a0001 | c0001 | t0005 | g0122 | AFR | ACB | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
HG02300 | hp1 | a0001 | c0001 | t0003 | g0069 | AMR | PEL | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
HG02300 | hp2 | a0001 | c0001 | t0003 | g0233 | AMR | PEL | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
HG02451 | hp1 | a0001 | c0001 | t0005 | g0147 | AFR | ACB | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
HG02451 | hp2 | a0001 | c0001 | t0005 | g0278 | AFR | ACB | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
HG02572 | hp1 | a0001 | c0001 | t0043 | g0087 | AFR | GWD | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
HG02572 | hp2 | a0001 | c0001 | t0037 | g0012 | AFR | GWD | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
HG02602 | hp1 | a0001 | c0001 | t0002 | g0241 | SAS | PJL | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
HG02602 | hp2 | a0001 | c0001 | t0003 | g0011 | SAS | PJL | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
HG02615 | hp1 | a0001 | c0001 | t0015 | g0013 | AFR | GWD | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
HG02615 | hp2 | a0001 | c0001 | t0005 | g0131 | AFR | GWD | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
HG02622 | hp1 | a0001 | c0001 | t0002 | g0093 | AFR | GWD | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
HG02622 | hp2 | a0001 | c0001 | t0002 | g0149 | AFR | GWD | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
HG02630 | hp1 | a0001 | c0001 | t0004 | g0303 | AFR | GWD | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
HG02630 | hp2 | a0001 | c0001 | t0002 | g0089 | AFR | GWD | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
HG02723 | hp1 | a0001 | c0001 | t0004 | g0136 | AFR | GWD | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
HG02723 | hp2 | a0001 | c0002 | t0001 | g0163 | AFR | GWD | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
HG02735 | hp1 | a0001 | c0001 | t0021 | g0074 | SAS | PJL | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
HG02735 | hp2 | a0001 | c0001 | t0003 | g0226 | SAS | PJL | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
HG02738 | hp1 | a0001 | c0001 | t0010 | g0219 | SAS | PJL | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
HG02738 | hp2 | a0001 | c0001 | t0007 | g0121 | SAS | PJL | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
HG02809 | hp1 | a0001 | c0001 | t0002 | g0097 | AFR | GWD | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
HG02809 | hp2 | a0001 | c0001 | t0002 | g0138 | AFR | GWD | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
HG02818 | hp1 | a0001 | c0001 | t0002 | g0091 | AFR | GWD | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
HG02818 | hp2 | a0001 | c0001 | t0008 | g0035 | AFR | GWD | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
HG02895 | hp1 | a0001 | c0001 | t0002 | g0098 | AFR | GWD | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
HG02897 | hp1 | a0001 | c0001 | t0010 | g0002 | AFR | GWD | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
HG02897 | hp2 | a0001 | c0001 | t0041 | g0088 | AFR | GWD | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
HG02976 | hp1 | a0001 | c0001 | t0005 | g0123 | AFR | ESN | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
HG02976 | hp2 | a0001 | c0001 | t0042 | g0279 | AFR | ESN | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0076 | SAS | PJL | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
HG03017 | hp2 | a0001 | c0016 | t0005 | g0166 | SAS | PJL | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0139 | AFR | GWD | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
HG03041 | hp2 | a0001 | c0002 | t0049 | g0209 | AFR | GWD | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
HG03098 | hp1 | a0001 | c0001 | t0040 | g0109 | AFR | MSL | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
HG03098 | hp2 | a0001 | c0001 | t0035 | g0063 | AFR | MSL | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
HG03130 | hp1 | a0001 | c0001 | t0002 | g0008 | AFR | ESN | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
HG03130 | hp2 | a0001 | c0001 | t0002 | g0134 | AFR | ESN | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
HG03195 | hp1 | a0001 | c0001 | t0018 | g0203 | AFR | ESN | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
HG03195 | hp2 | a0001 | c0001 | t0005 | g0132 | AFR | ESN | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
HG03209 | hp1 | a0001 | c0001 | t0002 | g0298 | AFR | MSL | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
HG03209 | hp2 | a0001 | c0001 | t0002 | g0141 | AFR | MSL | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
HG03225 | hp1 | a0001 | c0001 | t0002 | g0009 | AFR | MSL | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
HG03225 | hp2 | a0001 | c0001 | t0005 | g0133 | AFR | MSL | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
HG03239 | hp1 | a0001 | c0001 | t0002 | g0270 | SAS | PJL | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0184 | SAS | PJL | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
HG03453 | hp1 | a0001 | c0001 | t0005 | g0126 | AFR | MSL | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
HG03453 | hp2 | a0001 | c0002 | t0006 | g0210 | AFR | MSL | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
HG03486 | hp1 | a0001 | c0002 | t0005 | g0208 | AFR | MSL | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
HG03486 | hp2 | a0001 | c0001 | t0002 | g0140 | AFR | MSL | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
HG03491 | hp1 | a0001 | c0001 | t0013 | g0022 | SAS | PJL | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0077 | SAS | PJL | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
HG03492 | hp1 | a0001 | c0001 | t0013 | g0018 | SAS | PJL | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0066 | SAS | PJL | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
HG03516 | hp1 | a0001 | c0001 | t0013 | g0046 | AFR | ESN | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
HG03516 | hp2 | a0001 | c0001 | t0015 | g0015 | AFR | ESN | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
HG03579 | hp1 | a0001 | c0001 | t0005 | g0276 | AFR | MSL | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
HG03579 | hp2 | a0001 | c0001 | t0002 | g0142 | AFR | MSL | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0150 | SAS | PJL | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
HG03669 | hp2 | a0001 | c0001 | t0009 | g0245 | SAS | PJL | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0119 | SAS | BEB | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
HG03834 | hp2 | a0001 | c0001 | t0003 | g0296 | SAS | BEB | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
HG04184 | hp1 | a0001 | c0001 | t0003 | g0244 | SAS | BEB | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
HG04184 | hp2 | a0001 | c0001 | t0004 | g0107 | SAS | BEB | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
HG04199 | hp1 | a0008 | c0007 | t0006 | g0206 | SAS | STU | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
HG04199 | hp2 | a0001 | c0001 | t0009 | g0221 | SAS | STU | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0185 | SAS | STU | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0155 | SAS | STU | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0127 | AFR | YRI | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
NA18522 | hp2 | a0001 | c0001 | t0044 | g0230 | AFR | YRI | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
NA18939 | hp1 | a0001 | c0001 | t0014 | g0201 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
NA18939 | hp2 | a0001 | c0001 | t0017 | g0224 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
NA18940 | hp1 | a0001 | c0001 | t0010 | g0007 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
NA18940 | hp2 | a0001 | c0001 | t0051 | g0113 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
NA18942 | hp1 | a0001 | c0001 | t0012 | g0036 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
NA18942 | hp2 | a0001 | c0001 | t0012 | g0043 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
NA18943 | hp1 | a0001 | c0001 | t0002 | g0080 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
NA18943 | hp2 | a0001 | c0001 | t0011 | g0057 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
NA18945 | hp2 | a0001 | c0001 | t0002 | g0205 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
NA18948 | hp1 | a0001 | c0001 | t0002 | g0120 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
NA18948 | hp2 | a0001 | c0001 | t0013 | g0027 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
NA18949 | hp2 | a0001 | c0001 | t0008 | g0001 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
NA18951 | hp1 | a0001 | c0001 | t0004 | g0254 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
NA18951 | hp2 | a0001 | c0001 | t0003 | g0195 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
NA18952 | hp1 | a0001 | c0001 | t0014 | g0004 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
NA18952 | hp2 | a0001 | c0013 | t0016 | g0288 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
NA18953 | hp1 | a0001 | c0001 | t0014 | g0004 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
NA18956 | hp1 | a0001 | c0001 | t0038 | g0272 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
NA18956 | hp2 | a0001 | c0001 | t0052 | g0154 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
NA18959 | hp1 | a0001 | c0001 | t0002 | g0252 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
NA18959 | hp2 | a0001 | c0001 | t0047 | g0099 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
NA18962 | hp1 | a0001 | c0001 | t0004 | g0085 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
NA18962 | hp2 | a0006 | c0009 | t0007 | g0293 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
NA18965 | hp2 | a0001 | c0001 | t0014 | g0196 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
NA18967 | hp1 | a0001 | c0001 | t0009 | g0040 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
NA18967 | hp2 | a0001 | c0001 | t0003 | g0280 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
NA18968 | hp1 | a0001 | c0001 | t0002 | g0225 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
NA18968 | hp2 | a0001 | c0001 | t0004 | g0111 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
NA18969 | hp2 | a0001 | c0001 | t0008 | g0260 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
NA18971 | hp1 | a0001 | c0001 | t0048 | g0289 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
NA18971 | hp2 | a0001 | c0001 | t0025 | g0204 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
NA18977 | hp1 | a0001 | c0001 | t0007 | g0261 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
NA18977 | hp2 | a0001 | c0001 | t0003 | g0193 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
NA18980 | hp2 | a0001 | c0001 | t0006 | g0096 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
NA18981 | hp1 | a0001 | c0001 | t0002 | g0255 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
NA18981 | hp2 | a0001 | c0001 | t0019 | g0202 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
NA18982 | hp1 | a0001 | c0001 | t0011 | g0021 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
NA18984 | hp2 | a0001 | c0001 | t0050 | g0104 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
NA18985 | hp1 | a0001 | c0001 | t0002 | g0169 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
NA18985 | hp2 | a0001 | c0001 | t0053 | g0081 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
NA18988 | hp2 | a0001 | c0001 | t0005 | g0291 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
NA18990 | hp1 | a0001 | c0001 | t0012 | g0048 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
NA18990 | hp2 | a0001 | c0001 | t0003 | g0273 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
NA18992 | hp1 | a0007 | c0008 | t0045 | g0269 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
NA18992 | hp2 | a0001 | c0011 | t0001 | g0214 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
NA18993 | hp1 | a0001 | c0001 | t0056 | g0056 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
NA18993 | hp2 | a0001 | c0001 | t0019 | g0171 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
NA18994 | hp1 | a0001 | c0001 | t0006 | g0100 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
NA18998 | hp1 | a0001 | c0001 | t0007 | g0181 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
NA18998 | hp2 | a0001 | c0001 | t0002 | g0162 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
NA18999 | hp1 | a0003 | c0017 | t0011 | g0055 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
NA18999 | hp2 | a0001 | c0001 | t0002 | g0179 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
NA19000 | hp1 | a0001 | c0010 | t0001 | g0295 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
NA19000 | hp2 | a0001 | c0001 | t0004 | g0177 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
NA19001 | hp1 | a0002 | c0018 | t0011 | g0033 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
NA19001 | hp2 | a0001 | c0001 | t0030 | g0039 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
NA19002 | hp2 | a0001 | c0001 | t0002 | g0198 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
NA19004 | hp1 | a0001 | c0001 | t0024 | g0222 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
NA19007 | hp2 | a0001 | c0001 | t0002 | g0106 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
NA19009 | hp1 | a0001 | c0001 | t0026 | g0248 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
NA19009 | hp2 | a0001 | c0001 | t0007 | g0180 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
NA19010 | hp1 | a0001 | c0001 | t0011 | g0300 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
NA19010 | hp2 | a0001 | c0001 | t0006 | g0083 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
NA19011 | hp1 | a0001 | c0001 | t0004 | g0082 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
NA19011 | hp2 | a0001 | c0001 | t0012 | g0031 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
NA19012 | hp1 | a0001 | c0001 | t0010 | g0283 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
NA19012 | hp2 | a0001 | c0001 | t0055 | g0153 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
NA19030 | hp1 | a0001 | c0001 | t0015 | g0014 | AFR | LWK | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
NA19030 | hp2 | a0001 | c0001 | t0002 | g0145 | AFR | LWK | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
NA19043 | hp1 | a0001 | c0001 | t0002 | g0301 | AFR | LWK | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
NA19043 | hp2 | a0001 | c0001 | t0010 | g0274 | AFR | LWK | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
NA19056 | hp2 | a0001 | c0001 | t0023 | g0178 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
NA19057 | hp1 | a0001 | c0001 | t0012 | g0044 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
NA19057 | hp2 | a0001 | c0001 | t0003 | g0284 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
NA19058 | hp1 | a0001 | c0001 | t0006 | g0058 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
NA19060 | hp1 | a0001 | c0001 | t0006 | g0084 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
NA19060 | hp2 | a0001 | c0001 | t0008 | g0020 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
NA19062 | hp1 | a0001 | c0001 | t0002 | g0112 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
NA19062 | hp2 | a0001 | c0001 | t0008 | g0053 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
NA19064 | hp1 | a0001 | c0001 | t0002 | g0240 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
NA19064 | hp2 | a0001 | c0001 | t0009 | g0050 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
NA19066 | hp1 | a0001 | c0003 | t0002 | g0297 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
NA19074 | hp2 | a0001 | c0001 | t0008 | g0001 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
NA19077 | hp1 | a0001 | c0001 | t0002 | g0190 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
NA19083 | hp1 | a0001 | c0001 | t0004 | g0199 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
NA19086 | hp1 | a0001 | c0001 | t0007 | g0290 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
NA19087 | hp1 | a0001 | c0001 | t0003 | g0299 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
NA19087 | hp2 | a0001 | c0001 | t0010 | g0237 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
NA19088 | hp1 | a0001 | c0001 | t0002 | g0130 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
NA20129 | hp1 | a0001 | c0001 | t0022 | g0292 | AFR | ASW | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
NA20129 | hp2 | a0001 | c0001 | t0002 | g0277 | AFR | ASW | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
NA20752 | hp1 | a0001 | c0001 | t0004 | g0067 | EUR | TSI | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
NA20752 | hp2 | a0001 | c0001 | t0009 | g0029 | EUR | TSI | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
NA20805 | hp1 | a0001 | c0001 | t0008 | g0024 | EUR | TSI | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
NA20805 | hp2 | a0001 | c0001 | t0002 | g0235 | EUR | TSI | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
NA20905 | hp1 | a0001 | c0001 | t0006 | g0231 | SAS | GIH | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
NA20905 | hp2 | a0001 | c0001 | t0031 | g0038 | SAS | GIH | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0118 | AMR | CLM | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
HG01123 | hp2 | a0001 | c0001 | t0003 | g0246 | AMR | CLM | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
HG02486 | hp1 | a0001 | c0001 | t0036 | g0211 | AFR | ACB | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
HG02486 | hp2 | a0001 | c0001 | t0002 | g0128 | AFR | ACB | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
HG06807 | hp1 | a0001 | c0001 | t0003 | g0075 | AFR | USA | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
HG06807 | hp2 | a0001 | c0001 | t0002 | g0144 | AFR | USA | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
NA20300 | hp1 | a0001 | c0001 | t0005 | g0124 | AFR | USA | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
NA20300 | hp2 | a0001 | c0012 | t0001 | g0094 | AFR | USA | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
NA21309 | hp1 | a0001 | c0001 | t0006 | g0016 | AFR | LWK | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
NA21309 | hp2 | a0001 | c0001 | t0046 | g0095 | AFR | LWK | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0006 | g0105 | REF | REF | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0032 | g0028 | REF | REF | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr13:57632775
|
G | T | 1 | a0002 | 1 | NA19001.hp1 | missense_variant | MODERATE | c.229G>T | p.Val77Leu | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/4 | 1032/8300 | 229/3480 | 77/1159 | chr13 | 57632775 | ||
chr13:57632992
|
C | T | 1 | a0003 | 1 | NA18999.hp1 | missense_variant | MODERATE | c.446C>T | p.Thr149Ile | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/4 | 1249/8300 | 446/3480 | 149/1159 | chr13 | 57632992 | ||
chr13:57633577
|
G | T | 1 | a0004 | 1 | HG00280.hp2 | missense_variant | MODERATE | c.1031G>T | p.Arg344Leu | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/4 | 1834/8300 | 1031/3480 | 344/1159 | chr13 | 57633577 | ||
chr13:57633964
|
C | T | 1 | a0005 | 1 | HG01069.hp2 | missense_variant | MODERATE | c.1418C>T | p.Thr473Ile | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/4 | 2221/8300 | 1418/3480 | 473/1159 | chr13 | 57633964 | ||
chr13:57666785
|
G | A | 1 | a0008 | 1 | HG04199.hp1 | missense_variant | MODERATE | c.2749G>A | p.Ala917Thr | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/4 | 3552/8300 | 2749/3480 | 917/1159 | chr13 | 57666785 | ||
chr13:57724954
|
G | C | 1 | a0007 | 1 | NA18992.hp1 | missense_variant | MODERATE | c.3140G>C | p.Cys1047Ser | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 4/4 | 3943/8300 | 3140/3480 | 1047/1159 | chr13 | 57724954 | ||
chr13:57725224
|
A | G | 1 | a0006 | 1 | NA18962.hp2 | missense_variant | MODERATE | c.3410A>G | p.Glu1137Gly | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 4/4 | 4213/8300 | 3410/3480 | 1137/1159 | chr13 | 57725224 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr13:57633054
|
C | T | 1 | a0001c0004 | 2 | HG02257.hp1 HG02258.hp1 |
synonymous_variant | LOW | c.508C>T | p.Leu170Leu | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/4 | 1311/8300 | 508/3480 | 170/1159 | chr13 | 57633054 | ||
chr13:57633326
|
A | G | 1 | a0001c0016 | 1 | HG03017.hp2 | synonymous_variant | LOW | c.780A>G | p.Thr260Thr | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/4 | 1583/8300 | 780/3480 | 260/1159 | chr13 | 57633326 | ||
chr13:57633647
|
C | A | 1 | a0001c0005 | 1 | HG02083.hp1 | synonymous_variant | LOW | c.1101C>A | p.Pro367Pro | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/4 | 1904/8300 | 1101/3480 | 367/1159 | chr13 | 57633647 | ||
chr13:57633749
|
G | A | 1 | a0001c0006 | 1 | HG01099.hp2 | synonymous_variant | LOW | c.1203G>A | p.Gly401Gly | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/4 | 2006/8300 | 1203/3480 | 401/1159 | chr13 | 57633749 | ||
chr13:57634136
|
G | C | 1 | a0001c0003 | 3 | HG00280.hp1 HG00621.hp2 NA19066.hp1 |
synonymous_variant | LOW | c.1590G>C | p.Thr530Thr | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/4 | 2393/8300 | 1590/3480 | 530/1159 | chr13 | 57634136 | ||
chr13:57634310
|
G | A | 1 | a0001c0002 | 4 | HG02723.hp2 HG03041.hp2 HG03453.hp2 others(1): Show |
synonymous_variant | LOW | c.1764G>A | p.Leu588Leu | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/4 | 2567/8300 | 1764/3480 | 588/1159 | chr13 | 57634310 | ||
chr13:57634661
|
G | T | 1 | a0001c0013 | 1 | NA18952.hp2 | synonymous_variant | LOW | c.2115G>T | p.Ser705Ser | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/4 | 2918/8300 | 2115/3480 | 705/1159 | chr13 | 57634661 | ||
chr13:57634781
|
C | G | 1 | a0001c0012 | 1 | NA20300.hp2 | synonymous_variant | LOW | c.2235C>G | p.Ala745Ala | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/4 | 3038/8300 | 2235/3480 | 745/1159 | chr13 | 57634781 | ||
chr13:57724694
|
A | G | 1 | a0001c0011 | 1 | NA18992.hp2 | synonymous_variant | LOW | c.2880A>G | p.Ala960Ala | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 4/4 | 3683/8300 | 2880/3480 | 960/1159 | chr13 | 57724694 | ||
chr13:57725003
|
C | G | 1 | a0001c0010 | 1 | NA19000.hp1 | synonymous_variant | LOW | c.3189C>G | p.Ala1063Ala | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 4/4 | 3992/8300 | 3189/3480 | 1063/1159 | chr13 | 57725003 | ||
chr13:57725255
|
A | G | 1 | a0007c0008 | 1 | NA18992.hp1 | synonymous_variant | LOW | c.3441A>G | p.Gln1147Gln | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 4/4 | 4244/8300 | 3441/3480 | 1147/1159 | chr13 | 57725255 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr13:57631780
|
G | A | 3 | a0001c0001t0017a0001c0001t0024a0001c0001t0025 | 4 | HG00597.hp2 NA18939.hp2 NA18971.hp2 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-767G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/4 | 767 | chr13 | 57631780 | |||||
chr13:57631787
|
GA | G | 59 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(56): Show | 264 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(261): Show |
5_prime_UTR_variant | MODIFIER | c.-750delA | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/4 | 750 | INFO_REALIGN_3_PRIME | chr13 | 57631787 | ||||
chr13:57631801
|
G | C | 2 | a0001c0001t0034a0001c0001t0035 | 2 | HG02257.hp2 HG03098.hp2 |
5_prime_UTR_variant | MODIFIER | c.-746G>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/4 | 746 | chr13 | 57631801 | |||||
chr13:57631803
|
T | C | 1 | a0001c0001t0036 | 1 | HG02486.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-744T>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/4 | chr13 | 57631803 | ||||||
chr13:57631875
|
A | C | 1 | a0001c0001t0056 | 1 | NA18993.hp1 | 5_prime_UTR_variant | MODIFIER | c.-672A>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/4 | 672 | chr13 | 57631875 | |||||
chr13:57632078
|
T | C | 2 | a0001c0001t0015a0001c0001t0037 | 4 | HG02572.hp2 HG02615.hp1 HG03516.hp2 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-469T>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/4 | 469 | chr13 | 57632078 | |||||
chr13:57632389
|
C | T | 1 | a0001c0001t0055 | 1 | NA19012.hp2 | 5_prime_UTR_variant | MODIFIER | c.-158C>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/4 | 158 | chr13 | 57632389 | |||||
chr13:57632485
|
C | T | 1 | a0001c0001t0033 | 1 | HG00544.hp2 | 5_prime_UTR_variant | MODIFIER | c.-62C>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/4 | 62 | chr13 | 57632485 | |||||
chr13:57725300
|
G | GA | 37 | a0001c0001t0002a0001c0001t0004a0001c0001t0005others(34): Show | 155 | HG00140.hp2 HG00544.hp1 HG00544.hp2 others(152): Show |
3_prime_UTR_variant | MODIFIER | c.*17dupA | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 4/4 | 18 | INFO_REALIGN_3_PRIME | chr13 | 57725300 | ||||
chr13:57725490
|
G | A | 1 | a0001c0001t0018 | 2 | HG02055.hp2 HG03195.hp1 |
3_prime_UTR_variant | MODIFIER | c.*196G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 4/4 | 196 | chr13 | 57725490 | |||||
chr13:57725549
|
G | A | 28 | a0001c0001t0001a0001c0001t0006a0001c0001t0010others(25): Show | 108 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(105): Show |
3_prime_UTR_variant | MODIFIER | c.*255G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 4/4 | 255 | chr13 | 57725549 | |||||
chr13:57726102
|
A | G | 5 | a0001c0001t0007a0001c0001t0023a0001c0001t0053others(2): Show | 17 | HG00323.hp1 HG00558.hp1 HG00673.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*808A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 4/4 | 808 | chr13 | 57726102 | |||||
chr13:57726159
|
T | C | 1 | a0001c0001t0034 | 1 | HG02257.hp2 | 3_prime_UTR_variant | MODIFIER | c.*865T>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 4/4 | 865 | chr13 | 57726159 | |||||
chr13:57726298
|
C | T | 1 | a0001c0001t0046 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1004C>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 4/4 | 1004 | chr13 | 57726298 | |||||
chr13:57726309
|
A | C | 3 | a0001c0001t0024a0001c0001t0026a0007c0008t0045 | 3 | NA18992.hp1 NA19004.hp1 NA19009.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1015A>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 4/4 | 1015 | chr13 | 57726309 | |||||
chr13:57726625
|
G | A | 1 | a0001c0001t0050 | 1 | NA18984.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1331G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 4/4 | 1331 | chr13 | 57726625 | |||||
chr13:57726724
|
T | C | 2 | a0001c0001t0023a0001c0001t0053 | 3 | HG02129.hp1 NA18985.hp2 NA19056.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1430T>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 4/4 | 1430 | chr13 | 57726724 | |||||
chr13:57726737
|
C | T | 1 | a0001c0001t0044 | 1 | NA18522.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1443C>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 4/4 | 1443 | chr13 | 57726737 | |||||
chr13:57727204
|
A | T | 1 | a0001c0001t0043 | 1 | HG02572.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1910A>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 4/4 | 1910 | chr13 | 57727204 | |||||
chr13:57727438
|
T | C | 1 | a0001c0001t0038 | 1 | NA18956.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2144T>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 4/4 | 2144 | chr13 | 57727438 | |||||
chr13:57727718
|
G | C | 7 | a0001c0001t0006a0001c0001t0013a0001c0001t0036others(4): Show | 22 | HG00140.hp2 HG01069.hp2 HG01106.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*2424G>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 4/4 | 2424 | chr13 | 57727718 | |||||
chr13:57727977
|
G | A | 72 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(69): Show | 307 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(304): Show |
3_prime_UTR_variant | MODIFIER | c.*2683G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 4/4 | 2683 | chr13 | 57727977 | |||||
chr13:57728010
|
A | T | 1 | a0001c0001t0029 | 1 | HG00673.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2716A>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 4/4 | 2716 | chr13 | 57728010 | |||||
chr13:57728304
|
G | T | 1 | a0001c0002t0049 | 1 | HG03041.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3010G>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 4/4 | 3010 | chr13 | 57728304 | |||||
chr13:57728387
|
A | G | 1 | a0001c0001t0014 | 4 | NA18939.hp1 NA18952.hp1 NA18953.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3093A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 4/4 | 3093 | chr13 | 57728387 | |||||
chr13:57728478
|
T | C | 1 | a0001c0001t0039 | 1 | HG01109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3184T>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 4/4 | 3184 | chr13 | 57728478 | |||||
chr13:57728517
|
T | TA | 7 | a0001c0001t0020a0001c0001t0030a0001c0001t0039others(4): Show | 8 | HG01081.hp2 HG01109.hp2 HG01346.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*3246dupA | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 4/4 | 3247 | INFO_REALIGN_3_PRIME | chr13 | 57728517 | ||||
chr13:57728517
|
TA | T | 13 | a0001c0001t0005a0001c0001t0007a0001c0001t0010others(10): Show | 47 | HG00323.hp1 HG00558.hp1 HG00597.hp2 others(44): Show |
3_prime_UTR_variant | MODIFIER | c.*3246delA | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 4/4 | 3246 | INFO_REALIGN_3_PRIME | chr13 | 57728517 | ||||
chr13:57728517
|
TAA | T | 33 | a0001c0001t0001a0001c0001t0004a0001c0001t0006others(30): Show | 130 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(127): Show |
3_prime_UTR_variant | MODIFIER | c.*3245_*3246delAA | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 4/4 | 3245 | INFO_REALIGN_3_PRIME | chr13 | 57728517 | ||||
chr13:57728703
|
G | A | 1 | a0001c0001t0042 | 1 | HG02976.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3409G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 4/4 | 3409 | chr13 | 57728703 | |||||
chr13:57728707
|
G | A | 1 | a0001c0001t0041 | 1 | HG02897.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3413G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 4/4 | 3413 | chr13 | 57728707 | |||||
chr13:57728907
|
A | G | 1 | a0001c0001t0031 | 1 | NA20905.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3613A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 4/4 | 3613 | chr13 | 57728907 | |||||
chr13:57728943
|
G | A | 4 | a0001c0001t0016a0001c0001t0048a0001c0005t0028others(1): Show | 5 | HG02074.hp1 HG02080.hp1 HG02083.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3649G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 4/4 | 3649 | chr13 | 57728943 | |||||
chr13:57728949
|
T | C | 1 | a0001c0001t0041 | 1 | HG02897.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3655T>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 4/4 | 3655 | chr13 | 57728949 | |||||
chr13:57729037
|
G | A | 1 | a0001c0001t0044 | 1 | NA18522.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3743G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 4/4 | 3743 | chr13 | 57729037 | |||||
chr13:57729073
|
T | C | 1 | a0001c0001t0040 | 1 | HG03098.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3779T>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 4/4 | 3779 | chr13 | 57729073 | |||||
chr13:57729212
|
A | G | 1 | a0001c0001t0018 | 2 | HG02055.hp2 HG03195.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3918A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 4/4 | 3918 | chr13 | 57729212 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr13:57635244
|
C | T | 1 | a0001c0001t0004g0303 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2565+133C>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57635244 | ||||||
chr13:57636343
|
T | A | 2 | a0001c0001t0002g0008a0001c0001t0002g0009 | 2 | HG03130.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.2565+1232T>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57636343 | ||||||
chr13:57636383
|
A | G | 1 | a0001c0001t0009g0302 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.2565+1272A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57636383 | ||||||
chr13:57636743
|
A | G | 1 | a0001c0001t0002g0301 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2565+1632A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57636743 | ||||||
chr13:57636779
|
A | T | 1 | a0001c0001t0011g0300 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.2565+1668A>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57636779 | ||||||
chr13:57636917
|
G | T | 52 | a0001c0001t0001g0007a0001c0001t0001g0257a0001c0001t0001g0258others(49): Show | 52 | HG00280.hp1 HG00544.hp1 HG00597.hp1 others(49): Show |
intron_variant | MODIFIER | c.2565+1806G>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57636917 | ||||||
chr13:57637113
|
C | T | 2 | a0001c0001t0002g0250a0001c0001t0020g0249 | 2 | HG01074.hp1 HG01346.hp2 |
intron_variant | MODIFIER | c.2565+2002C>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57637113 | ||||||
chr13:57637469
|
A | G | 1 | a0001c0001t0026g0248 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.2565+2358A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57637469 | ||||||
chr13:57638040
|
A | C | 1 | a0001c0001t0034g0247 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2565+2929A>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57638040 | ||||||
chr13:57638272
|
T | A | 2 | a0001c0001t0001g0010a0001c0001t0003g0011 | 2 | HG01361.hp1 HG02602.hp2 |
intron_variant | MODIFIER | c.2565+3161T>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57638272 | ||||||
chr13:57638470
|
T | C | 4 | a0001c0001t0015g0013a0001c0001t0015g0014a0001c0001t0015g0015others(1): Show | 4 | HG02572.hp2 HG02615.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.2565+3359T>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57638470 | ||||||
chr13:57638507
|
C | T | 259 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(256): Show | 263 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(260): Show |
intron_variant | MODIFIER | c.2565+3396C>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57638507 | ||||||
chr13:57639081
|
T | C | 1 | a0001c0001t0001g0059 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2565+3970T>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57639081 | ||||||
chr13:57639178
|
T | A | 4 | a0001c0001t0001g0059a0001c0001t0018g0060a0001c0004t0005g0061others(1): Show | 4 | HG02055.hp2 HG02257.hp1 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.2565+4067T>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57639178 | ||||||
chr13:57639260
|
C | G | 1 | a0001c0001t0003g0246 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.2565+4149C>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57639260 | ||||||
chr13:57639358
|
A | C | 2 | a0001c0001t0002g0008a0001c0001t0002g0009 | 2 | HG03130.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.2565+4247A>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57639358 | ||||||
chr13:57639502
|
A | T | 1 | a0001c0001t0006g0058 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.2565+4391A>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57639502 | ||||||
chr13:57639711
|
T | C | 1 | a0001c0001t0002g0301 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2565+4600T>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57639711 | ||||||
chr13:57640395
|
A | C | 164 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0059others(161): Show | 168 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(165): Show |
intron_variant | MODIFIER | c.2565+5284A>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57640395 | ||||||
chr13:57640611
|
C | T | 52 | a0001c0001t0001g0002a0001c0001t0001g0103a0001c0001t0001g0110others(49): Show | 52 | HG00323.hp1 HG01081.hp2 HG01099.hp2 others(49): Show |
intron_variant | MODIFIER | c.2565+5500C>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57640611 | ||||||
chr13:57640617
|
G | T | 1 | a0001c0001t0009g0245 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.2565+5506G>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57640617 | ||||||
chr13:57640713
|
T | C | 2 | a0001c0001t0034g0247a0001c0001t0035g0063 | 2 | HG02257.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.2565+5602T>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57640713 | ||||||
chr13:57640774
|
A | T | 1 | a0001c0001t0009g0245 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.2565+5663A>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57640774 | ||||||
chr13:57640794
|
A | G | 3 | a0001c0001t0011g0057a0001c0001t0056g0056a0003c0017t0011g0055 | 3 | NA18943.hp2 NA18993.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.2565+5683A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57640794 | ||||||
chr13:57640890
|
A | C | 1 | a0001c0001t0003g0299 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.2565+5779A>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57640890 | ||||||
chr13:57640893
|
C | T | 1 | a0001c0001t0002g0298 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2565+5782C>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57640893 | ||||||
chr13:57640894
|
G | A | 2 | a0001c0001t0002g0008a0001c0001t0002g0009 | 2 | HG03130.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.2565+5783G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57640894 | ||||||
chr13:57640918
|
A | G | 2 | a0001c0001t0034g0247a0001c0001t0035g0063 | 2 | HG02257.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.2565+5807A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57640918 | ||||||
chr13:57640924
|
A | T | 6 | a0001c0001t0002g0241a0001c0001t0002g0250a0001c0001t0003g0244others(3): Show | 6 | HG00140.hp2 HG01074.hp1 HG01346.hp2 others(3): Show |
intron_variant | MODIFIER | c.2565+5813A>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57640924 | ||||||
chr13:57641008
|
G | A | 207 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(204): Show | 211 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(208): Show |
intron_variant | MODIFIER | c.2565+5897G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57641008 | ||||||
chr13:57641142
|
G | A | 207 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(204): Show | 211 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(208): Show |
intron_variant | MODIFIER | c.2565+6031G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57641142 | ||||||
chr13:57641558
|
GA | G | 24 | a0001c0001t0001g0103a0001c0001t0001g0115a0001c0001t0001g0258others(21): Show | 24 | HG00280.hp2 HG00323.hp1 HG00735.hp2 others(21): Show |
intron_variant | MODIFIER | c.2565+6477delA | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 57641558 | |||||
chr13:57641558
|
GAA | G | 8 | a0001c0001t0001g0049a0001c0001t0002g0102a0001c0001t0004g0111others(5): Show | 8 | HG01069.hp2 HG01496.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.2565+6476_2565+647 others(6): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 57641558 | |||||
chr13:57641558
|
GAAA | G | 11 | a0001c0001t0001g0059a0001c0001t0001g0118a0001c0001t0001g0119others(8): Show | 11 | HG00673.hp1 HG01123.hp1 HG01123.hp2 others(8): Show |
intron_variant | MODIFIER | c.2565+6475_2565+647 others(7): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 57641558 | |||||
chr13:57641558
|
GAAAA | G | 9 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0079others(6): Show | 9 | HG01109.hp1 HG01934.hp2 HG02080.hp2 others(6): Show |
intron_variant | MODIFIER | c.2565+6474_2565+647 others(8): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 57641558 | |||||
chr13:57641558
|
GAAAAA | G | 19 | a0001c0001t0001g0218a0001c0001t0001g0281a0001c0001t0001g0282others(16): Show | 20 | HG00323.hp2 HG00621.hp1 HG01168.hp2 others(17): Show |
intron_variant | MODIFIER | c.2565+6473_2565+647 others(9): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 57641558 | |||||
chr13:57641558
|
GAAAAAA | G | 10 | a0001c0001t0001g0161a0001c0001t0002g0112a0001c0001t0002g0162others(7): Show | 10 | HG00735.hp1 HG01074.hp1 HG01099.hp2 others(7): Show |
intron_variant | MODIFIER | c.2565+6472_2565+647 others(10): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 57641558 | |||||
chr13:57641558
|
GAAAAAAA | G | 21 | a0001c0001t0001g0007a0001c0001t0001g0101a0001c0001t0002g0144others(18): Show | 21 | HG00140.hp2 HG00280.hp1 HG01081.hp2 others(18): Show |
intron_variant | MODIFIER | c.2565+6471_2565+647 others(11): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 57641558 | |||||
chr13:57641558
|
GAAAAAAA others(1): Show |
G | 14 | a0001c0001t0001g0139a0001c0001t0001g0146a0001c0001t0002g0008others(11): Show | 14 | HG00639.hp1 HG01975.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.2565+6470_2565+647 others(12): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 57641558 | |||||
chr13:57641558
|
GAAAAAAA others(2): Show |
G | 22 | a0001c0001t0002g0223a0001c0001t0002g0236a0001c0001t0003g0299others(19): Show | 22 | HG00621.hp2 HG00673.hp2 HG01433.hp1 others(19): Show |
intron_variant | MODIFIER | c.2565+6469_2565+647 others(13): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 57641558 | |||||
chr13:57641558
|
GAAAAAAA others(3): Show |
G | 15 | a0001c0001t0001g0167a0001c0001t0001g0232a0001c0001t0001g0238others(12): Show | 15 | HG00140.hp1 HG00738.hp1 HG01099.hp1 others(12): Show |
intron_variant | MODIFIER | c.2565+6468_2565+647 others(14): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 57641558 | |||||
chr13:57641558
|
GAAAAAAA others(4): Show |
G | 20 | a0001c0001t0001g0006a0001c0001t0002g0005a0001c0001t0002g0134others(17): Show | 22 | HG00741.hp1 HG00741.hp2 HG01081.hp1 others(19): Show |
intron_variant | MODIFIER | c.2565+6467_2565+647 others(15): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 57641558 | |||||
chr13:57641558
|
GAAAAAAA others(5): Show |
G | 5 | a0001c0001t0001g0213a0001c0001t0002g0140a0001c0001t0002g0169others(2): Show | 5 | HG01074.hp2 HG02897.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.2565+6466_2565+647 others(16): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 57641558 | |||||
chr13:57641558
|
GAAAAAAA others(6): Show |
G | 18 | a0001c0001t0001g0175a0001c0001t0001g0257a0001c0001t0001g0271others(15): Show | 18 | HG00544.hp1 HG02129.hp1 HG02615.hp1 others(15): Show |
intron_variant | MODIFIER | c.2565+6465_2565+647 others(17): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 57641558 | |||||
chr13:57641558
|
GAAAAAAA others(7): Show |
G | 10 | a0001c0001t0002g0089a0001c0001t0002g0091a0001c0001t0002g0234others(7): Show | 10 | HG01255.hp1 HG01496.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.2565+6464_2565+647 others(18): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 57641558 | |||||
chr13:57641558
|
GAAAAAAA others(8): Show |
G | 3 | a0001c0001t0002g0097a0001c0001t0033g0229a0001c0001t0044g0230 | 3 | HG00544.hp2 HG02809.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.2565+6463_2565+647 others(19): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 57641558 | |||||
chr13:57641558
|
GAAAAAAA others(9): Show |
G | 2 | a0001c0001t0005g0278a0001c0001t0042g0279 | 2 | HG02451.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.2565+6462_2565+647 others(20): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 57641558 | |||||
chr13:57641571
|
A | T | 1 | a0001c0001t0010g0237 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.2565+6460A>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57641571 | ||||||
chr13:57641572
|
AAAAAAAA others(10): Show |
A | 2 | a0001c0001t0010g0274a0001c0001t0034g0247 | 2 | HG02257.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.2565+6463_2565+647 others(21): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 57641572 | |||||
chr13:57641573
|
A | T | 3 | a0001c0001t0003g0280a0001c0001t0010g0237a0001c0003t0002g0297 | 3 | NA18967.hp2 NA19066.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.2565+6462A>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57641573 | ||||||
chr13:57641573
|
AAAAAAAA others(9): Show |
A | 1 | a0001c0001t0004g0215 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.2565+6464_2565+647 others(20): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 57641573 | |||||
chr13:57641574
|
AAAAAAAA others(8): Show |
A | 24 | a0001c0001t0001g0184a0001c0001t0001g0185a0001c0001t0001g0186others(21): Show | 25 | HG00558.hp1 HG00558.hp2 HG00738.hp2 others(22): Show |
intron_variant | MODIFIER | c.2565+6465_2565+647 others(19): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 57641574 | |||||
chr13:57641574
|
AAAAAAAA others(10): Show |
A | 1 | a0001c0004t0005g0062 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2565+6465_2565+648 others(21): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 57641574 | |||||
chr13:57641575
|
A | T | 10 | a0001c0001t0001g0258a0001c0001t0001g0259a0001c0001t0002g0093others(7): Show | 10 | HG01261.hp1 HG01515.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.2565+6464A>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57641575 | ||||||
chr13:57641575
|
AAAAAAAA others(7): Show |
A | 2 | a0001c0001t0001g0170a0001c0001t0019g0171 | 2 | HG01175.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.2565+6466_2565+647 others(18): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 57641575 | |||||
chr13:57641575
|
AAAAAAAA others(9): Show |
A | 2 | a0001c0001t0002g0141a0001c0001t0002g0142 | 2 | HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.2565+6466_2565+648 others(20): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 57641575 | |||||
chr13:57641575
|
AAAAAAAA others(15): Show |
A | 1 | a0001c0001t0004g0143 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2565+6466_2565+648 others(26): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 57641575 | |||||
chr13:57641576
|
AAAAAAAA others(6): Show |
A | 1 | a0001c0001t0002g0252 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.2565+6467_2565+647 others(17): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 57641576 | |||||
chr13:57641576
|
AAAAAAAA others(8): Show |
A | 5 | a0001c0001t0001g0155a0001c0001t0001g0156a0001c0001t0001g0157others(2): Show | 5 | HG01346.hp1 HG01433.hp2 HG04204.hp2 others(2): Show |
intron_variant | MODIFIER | c.2565+6467_2565+648 others(19): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 57641576 | |||||
chr13:57641577
|
A | AT | 4 | a0001c0001t0002g0080a0001c0001t0005g0131a0001c0001t0017g0152others(1): Show | 4 | HG00597.hp2 HG02615.hp2 NA18943.hp1 others(1): Show |
intron_variant | MODIFIER | c.2565+6466_2565+646 others(5): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57641577 | ||||||
chr13:57641577
|
A | T | 18 | a0001c0001t0001g0059a0001c0001t0001g0101a0001c0001t0001g0258others(15): Show | 18 | HG00280.hp1 HG01074.hp1 HG01261.hp1 others(15): Show |
intron_variant | MODIFIER | c.2565+6466A>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57641577 | ||||||
chr13:57641577
|
AAAAAAAA others(5): Show |
A | 1 | a0001c0001t0002g0251 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.2565+6468_2565+647 others(16): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 57641577 | |||||
chr13:57641577
|
AAAAAAAA others(9): Show |
A | 2 | a0001c0001t0001g0002a0001c0001t0010g0002 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.2565+6468_2565+648 others(20): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 57641577 | |||||
chr13:57641578
|
AAAAAAAA others(4): Show |
A | 1 | a0001c0001t0001g0127 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2565+6469_2565+647 others(15): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 57641578 | |||||
chr13:57641578
|
AAAAAAAA others(6): Show |
A | 1 | a0001c0001t0002g0128 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2565+6469_2565+648 others(17): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 57641578 | |||||
chr13:57641578
|
AAAAAAAA others(8): Show |
A | 1 | a0001c0001t0001g0150 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.2565+6469_2565+648 others(19): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 57641578 | |||||
chr13:57641579
|
A | T | 44 | a0001c0001t0001g0059a0001c0001t0001g0101a0001c0001t0001g0129others(41): Show | 44 | HG00280.hp1 HG00323.hp2 HG00597.hp2 others(41): Show |
intron_variant | MODIFIER | c.2565+6468A>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57641579 | ||||||
chr13:57641579
|
AAAAAAAA others(3): Show |
A | 1 | a0001c0001t0009g0054 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.2565+6470_2565+647 others(14): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 57641579 | |||||
chr13:57641580
|
AAAAAAAA others(12): Show |
A | 1 | a0001c0001t0040g0109 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2565+6471_2565+648 others(23): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 57641580 | |||||
chr13:57641581
|
A | T | 70 | a0001c0001t0001g0059a0001c0001t0001g0101a0001c0001t0001g0110others(67): Show | 71 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(68): Show |
intron_variant | MODIFIER | c.2565+6470A>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57641581 | ||||||
chr13:57641583
|
A | T | 101 | a0001c0001t0001g0007a0001c0001t0001g0059a0001c0001t0001g0101others(98): Show | 102 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(99): Show |
intron_variant | MODIFIER | c.2565+6472A>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57641583 | ||||||
chr13:57641585
|
A | T | 139 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0059others(136): Show | 142 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(139): Show |
intron_variant | MODIFIER | c.2565+6474A>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57641585 | ||||||
chr13:57641587
|
A | AT | 4 | a0001c0001t0009g0029a0001c0001t0012g0031a0001c0001t0026g0248others(1): Show | 4 | HG01515.hp2 NA19009.hp1 NA19011.hp2 others(1): Show |
intron_variant | MODIFIER | c.2565+6476_2565+647 others(5): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57641587 | ||||||
chr13:57641587
|
A | T | 181 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0049others(178): Show | 184 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(181): Show |
intron_variant | MODIFIER | c.2565+6476A>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57641587 | ||||||
chr13:57641588
|
AT | A | 6 | a0001c0001t0006g0016a0001c0001t0006g0058a0001c0001t0008g0001others(3): Show | 7 | HG01257.hp1 HG03492.hp1 NA18949.hp2 others(4): Show |
intron_variant | MODIFIER | c.2565+6478delT | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57641588 | ||||||
chr13:57641588
|
ATATATAT others(10): Show |
A | 1 | a0001c0001t0003g0064 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.2565+6478_2565+649 others(21): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57641588 | ||||||
chr13:57641589
|
T | A | 1 | a0001c0001t0008g0017 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.2565+6478T>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57641589 | ||||||
chr13:57641591
|
T | A | 1 | a0001c0001t0006g0016 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2565+6480T>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57641591 | ||||||
chr13:57641622
|
A | G | 2 | a0001c0001t0003g0262a0001c0001t0003g0263 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.2565+6511A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57641622 | ||||||
chr13:57641623
|
T | A | 2 | a0001c0001t0003g0262a0001c0001t0003g0263 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.2565+6512T>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57641623 | ||||||
chr13:57641779
|
G | A | 1 | a0001c0001t0002g0266 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2565+6668G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57641779 | ||||||
chr13:57641995
|
A | C | 1 | a0001c0001t0001g0103 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.2565+6884A>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57641995 | ||||||
chr13:57642060
|
G | A | 26 | a0001c0001t0001g0002a0001c0001t0001g0103a0001c0001t0001g0110others(23): Show | 26 | HG00323.hp1 HG01081.hp2 HG01099.hp2 others(23): Show |
intron_variant | MODIFIER | c.2565+6949G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57642060 | ||||||
chr13:57642186
|
C | A | 46 | a0001c0001t0001g0150a0001c0001t0001g0155a0001c0001t0001g0156others(43): Show | 47 | HG00544.hp2 HG00558.hp1 HG00558.hp2 others(44): Show |
intron_variant | MODIFIER | c.2565+7075C>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57642186 | ||||||
chr13:57642330
|
T | C | 1 | a0001c0001t0002g0141 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2565+7219T>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57642330 | ||||||
chr13:57642398
|
A | G | 5 | a0001c0001t0002g0235a0001c0001t0003g0151a0001c0001t0003g0220others(2): Show | 5 | HG00323.hp2 HG01069.hp2 HG01934.hp2 others(2): Show |
intron_variant | MODIFIER | c.2565+7287A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57642398 | ||||||
chr13:57642443
|
A | G | 1 | a0001c0001t0019g0202 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.2565+7332A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57642443 | ||||||
chr13:57642674
|
G | C | 1 | a0001c0001t0016g0286 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.2565+7563G>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57642674 | ||||||
chr13:57643012
|
C | T | 2 | a0001c0001t0002g0008a0001c0001t0002g0009 | 2 | HG03130.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.2565+7901C>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57643012 | ||||||
chr13:57643081
|
T | C | 1 | a0001c0001t0001g0170 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.2565+7970T>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57643081 | ||||||
chr13:57643180
|
T | G | 6 | a0001c0001t0002g0241a0001c0001t0002g0250a0001c0001t0003g0244others(3): Show | 6 | HG00140.hp2 HG01074.hp1 HG01346.hp2 others(3): Show |
intron_variant | MODIFIER | c.2565+8069T>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57643180 | ||||||
chr13:57643277
|
G | A | 205 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(202): Show | 209 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(206): Show |
intron_variant | MODIFIER | c.2565+8166G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57643277 | ||||||
chr13:57643569
|
G | A | 99 | a0001c0001t0001g0006a0001c0001t0001g0150a0001c0001t0001g0155others(96): Show | 103 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(100): Show |
intron_variant | MODIFIER | c.2565+8458G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57643569 | ||||||
chr13:57643724
|
T | C | 1 | a0001c0001t0006g0058 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.2565+8613T>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57643724 | ||||||
chr13:57643772
|
A | C | 1 | a0001c0001t0018g0060 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2565+8661A>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57643772 | ||||||
chr13:57643953
|
A | G | 6 | a0001c0001t0002g0277a0001c0001t0005g0275a0001c0001t0005g0276others(3): Show | 6 | HG01496.hp1 HG02451.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.2565+8842A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57643953 | ||||||
chr13:57644485
|
A | G | 1 | a0001c0001t0018g0060 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2565+9374A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57644485 | ||||||
chr13:57644512
|
G | A | 1 | a0001c0001t0001g0059 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2565+9401G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57644512 | ||||||
chr13:57644526
|
T | TA | 57 | a0001c0001t0001g0007a0001c0001t0001g0218a0001c0001t0001g0238others(54): Show | 57 | HG00280.hp1 HG00544.hp1 HG00597.hp1 others(54): Show |
intron_variant | MODIFIER | c.2565+9424dupA | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 57644526 | |||||
chr13:57644556
|
C | G | 2 | a0001c0001t0014g0004a0001c0001t0014g0201 | 3 | NA18939.hp1 NA18952.hp1 NA18953.hp1 |
intron_variant | MODIFIER | c.2565+9445C>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57644556 | ||||||
chr13:57644593
|
C | T | 2 | a0001c0001t0001g0200a0001c0001t0004g0199 | 2 | NA19066.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.2565+9482C>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57644593 | ||||||
chr13:57644596
|
C | T | 26 | a0001c0001t0001g0002a0001c0001t0001g0103a0001c0001t0001g0110others(23): Show | 26 | HG00323.hp1 HG01081.hp2 HG01099.hp2 others(23): Show |
intron_variant | MODIFIER | c.2565+9485C>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57644596 | ||||||
chr13:57644966
|
G | A | 3 | a0001c0001t0002g0106a0001c0001t0002g0112a0001c0001t0002g0130 | 3 | NA19007.hp2 NA19062.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.2565+9855G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57644966 | ||||||
chr13:57645165
|
C | T | 1 | a0001c0001t0002g0097 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2565+10054C>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57645165 | ||||||
chr13:57646461
|
A | C | 52 | a0001c0001t0001g0002a0001c0001t0001g0103a0001c0001t0001g0110others(49): Show | 52 | HG00323.hp1 HG01081.hp2 HG01099.hp2 others(49): Show |
intron_variant | MODIFIER | c.2565+11350A>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57646461 | ||||||
chr13:57646676
|
T | C | 2 | a0001c0001t0001g0065a0001c0001t0001g0066 | 2 | HG00639.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.2565+11565T>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57646676 | ||||||
chr13:57646689
|
T | C | 1 | a0001c0004t0005g0062 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2565+11578T>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57646689 | ||||||
chr13:57646699
|
G | A | 19 | a0001c0001t0001g0010a0001c0001t0001g0065a0001c0001t0001g0066others(16): Show | 19 | HG00639.hp2 HG01106.hp1 HG01256.hp2 others(16): Show |
intron_variant | MODIFIER | c.2565+11588G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57646699 | ||||||
chr13:57646734
|
C | T | 1 | a0001c0001t0003g0296 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.2565+11623C>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57646734 | ||||||
chr13:57646764
|
T | A | 1 | a0001c0001t0007g0121 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.2565+11653T>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57646764 | ||||||
chr13:57646905
|
C | T | 1 | a0001c0001t0001g0139 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2565+11794C>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57646905 | ||||||
chr13:57646911
|
C | A | 1 | a0001c0001t0003g0246 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.2565+11800C>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57646911 | ||||||
chr13:57646922
|
T | G | 2 | a0001c0001t0002g0005a0001c0001t0003g0226 | 3 | HG00741.hp2 HG01192.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.2565+11811T>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57646922 | ||||||
chr13:57646947
|
A | T | 1 | a0001c0001t0003g0226 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.2565+11836A>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57646947 | ||||||
chr13:57647541
|
C | T | 1 | a0001c0001t0002g0198 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.2565+12430C>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57647541 | ||||||
chr13:57648161
|
T | C | 1 | a0001c0001t0011g0182 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.2565+13050T>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57648161 | ||||||
chr13:57648190
|
A | G | 2 | a0001c0004t0005g0061a0001c0004t0005g0062 | 2 | HG02257.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.2565+13079A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57648190 | ||||||
chr13:57648295
|
G | T | 10 | a0001c0001t0009g0040a0001c0001t0009g0050a0001c0001t0011g0057others(7): Show | 10 | HG02083.hp1 NA18942.hp2 NA18943.hp2 others(7): Show |
intron_variant | MODIFIER | c.2565+13184G>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57648295 | ||||||
chr13:57648378
|
G | A | 52 | a0001c0001t0001g0002a0001c0001t0001g0103a0001c0001t0001g0110others(49): Show | 52 | HG00323.hp1 HG01081.hp2 HG01099.hp2 others(49): Show |
intron_variant | MODIFIER | c.2565+13267G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57648378 | ||||||
chr13:57648544
|
T | A | 237 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(234): Show | 241 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(238): Show |
intron_variant | MODIFIER | c.2565+13433T>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57648544 | ||||||
chr13:57648673
|
T | C | 1 | a0001c0012t0001g0094 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2565+13562T>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57648673 | ||||||
chr13:57648714
|
A | G | 2 | a0001c0001t0034g0247a0001c0001t0035g0063 | 2 | HG02257.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.2565+13603A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57648714 | ||||||
chr13:57649038
|
A | G | 1 | a0001c0001t0012g0044 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.2565+13927A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57649038 | ||||||
chr13:57649380
|
A | G | 1 | a0001c0001t0001g0059 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2565+14269A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57649380 | ||||||
chr13:57649583
|
A | T | 1 | a0001c0001t0001g0159 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.2565+14472A>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57649583 | ||||||
chr13:57649675
|
T | C | 52 | a0001c0001t0001g0002a0001c0001t0001g0103a0001c0001t0001g0110others(49): Show | 52 | HG00323.hp1 HG01081.hp2 HG01099.hp2 others(49): Show |
intron_variant | MODIFIER | c.2565+14564T>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57649675 | ||||||
chr13:57649896
|
T | C | 1 | a0001c0001t0001g0281 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.2565+14785T>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57649896 | ||||||
chr13:57649987
|
G | A | 4 | a0001c0001t0001g0059a0001c0001t0018g0060a0001c0004t0005g0061others(1): Show | 4 | HG02055.hp2 HG02257.hp1 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.2565+14876G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57649987 | ||||||
chr13:57650218
|
T | TTG | 40 | a0001c0001t0001g0103a0001c0001t0001g0110a0001c0001t0001g0115others(37): Show | 41 | HG00323.hp1 HG00621.hp1 HG00621.hp2 others(38): Show |
intron_variant | MODIFIER | c.2565+15149_2565+15 others(8): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 57650218 | |||||
chr13:57650218
|
T | TTGTG | 47 | a0001c0001t0001g0002a0001c0001t0001g0127a0001c0001t0001g0129others(44): Show | 47 | HG00544.hp1 HG00558.hp1 HG01069.hp2 others(44): Show |
intron_variant | MODIFIER | c.2565+15147_2565+15 others(10): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 57650218 | |||||
chr13:57650218
|
T | TTGTGTG | 43 | a0001c0001t0001g0059a0001c0001t0001g0161a0001c0001t0001g0175others(40): Show | 43 | HG00140.hp2 HG00280.hp1 HG00639.hp1 others(40): Show |
intron_variant | MODIFIER | c.2565+15145_2565+15 others(12): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 57650218 | |||||
chr13:57650218
|
T | TTGTGTGT others(1): Show |
55 | a0001c0001t0001g0006a0001c0001t0001g0139a0001c0001t0001g0150others(52): Show | 58 | HG00323.hp2 HG00558.hp2 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.2565+15143_2565+15 others(14): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 57650218 | |||||
chr13:57650218
|
T | TTGTGTGT others(3): Show |
10 | a0001c0001t0001g0167a0001c0001t0002g0266a0001c0001t0003g0195others(7): Show | 10 | HG00140.hp1 HG00544.hp2 HG01081.hp1 others(7): Show |
intron_variant | MODIFIER | c.2565+15141_2565+15 others(16): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 57650218 | |||||
chr13:57650218
|
T | TTGTGTGT others(5): Show |
4 | a0001c0001t0001g0197a0001c0001t0002g0141a0001c0001t0006g0168others(1): Show | 4 | HG01978.hp2 HG03209.hp2 NA18956.hp2 others(1): Show |
intron_variant | MODIFIER | c.2565+15139_2565+15 others(18): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 57650218 | |||||
chr13:57650218
|
TTG | T | 47 | a0001c0001t0001g0049a0001c0001t0001g0101a0001c0001t0001g0186others(44): Show | 47 | HG00280.hp2 HG00735.hp2 HG00738.hp2 others(44): Show |
intron_variant | MODIFIER | c.2565+15149_2565+15 others(8): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 57650218 | |||||
chr13:57650218
|
TTGTG | T | 13 | a0001c0001t0001g0184a0001c0001t0001g0185a0001c0001t0002g0093others(10): Show | 13 | HG01168.hp1 HG01192.hp1 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.2565+15147_2565+15 others(10): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 57650218 | |||||
chr13:57650218
|
TTGTGTG | T | 16 | a0001c0001t0001g0010a0001c0001t0001g0065a0001c0001t0001g0066others(13): Show | 16 | HG00639.hp2 HG01106.hp1 HG01256.hp2 others(13): Show |
intron_variant | MODIFIER | c.2565+15145_2565+15 others(12): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 57650218 | |||||
chr13:57650218
|
TTGTGTGT others(1): Show |
T | 4 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0003g0075others(1): Show | 4 | HG02735.hp1 HG03017.hp1 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.2565+15143_2565+15 others(14): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 57650218 | |||||
chr13:57650218
|
TTGTGTGT others(11): Show |
T | 1 | a0001c0001t0039g0267 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2565+15133_2565+15 others(24): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 57650218 | |||||
chr13:57650311
|
G | C | 56 | a0001c0001t0001g0007a0001c0001t0001g0238a0001c0001t0001g0257others(53): Show | 56 | HG00280.hp1 HG00544.hp1 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.2565+15200G>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57650311 | ||||||
chr13:57650986
|
C | T | 55 | a0001c0001t0001g0007a0001c0001t0001g0238a0001c0001t0001g0257others(52): Show | 55 | HG00280.hp1 HG00544.hp1 HG00597.hp1 others(52): Show |
intron_variant | MODIFIER | c.2566-15482C>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57650986 | ||||||
chr13:57651007
|
A | G | 26 | a0001c0001t0001g0127a0001c0001t0001g0139a0001c0001t0002g0128others(23): Show | 26 | HG01243.hp1 HG01884.hp2 HG01891.hp1 others(23): Show |
intron_variant | MODIFIER | c.2566-15461A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57651007 | ||||||
chr13:57651036
|
A | T | 18 | a0001c0001t0001g0010a0001c0001t0001g0065a0001c0001t0001g0066others(15): Show | 18 | HG00639.hp2 HG01106.hp1 HG01256.hp2 others(15): Show |
intron_variant | MODIFIER | c.2566-15432A>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57651036 | ||||||
chr13:57651304
|
A | G | 1 | a0001c0001t0006g0168 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.2566-15164A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57651304 | ||||||
chr13:57651356
|
G | GT | 17 | a0001c0001t0002g0091a0001c0001t0003g0041a0001c0001t0004g0092others(14): Show | 17 | HG00673.hp1 HG00735.hp2 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.2566-15089dupT | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 57651356 | |||||
chr13:57651356
|
GT | G | 188 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(185): Show | 192 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(189): Show |
intron_variant | MODIFIER | c.2566-15089delT | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 57651356 | |||||
chr13:57651359
|
T | G | 1 | a0001c0001t0010g0283 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.2566-15109T>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57651359 | ||||||
chr13:57651369
|
T | G | 1 | a0001c0001t0001g0103 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.2566-15099T>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57651369 | ||||||
chr13:57651476
|
T | A | 1 | a0001c0001t0001g0155 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2566-14992T>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57651476 | ||||||
chr13:57651483
|
A | G | 3 | a0001c0001t0002g0005a0001c0001t0003g0226a0001c0001t0010g0237 | 4 | HG00741.hp2 HG01192.hp2 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.2566-14985A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57651483 | ||||||
chr13:57651568
|
T | G | 218 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(215): Show | 222 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(219): Show |
intron_variant | MODIFIER | c.2566-14900T>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57651568 | ||||||
chr13:57651574
|
G | A | 17 | a0001c0001t0001g0007a0001c0001t0001g0238a0001c0001t0002g0240others(14): Show | 17 | HG00621.hp1 HG02027.hp2 HG02074.hp1 others(14): Show |
intron_variant | MODIFIER | c.2566-14894G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57651574 | ||||||
chr13:57651612
|
A | G | 1 | a0001c0001t0012g0043 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.2566-14856A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57651612 | ||||||
chr13:57651707
|
C | A | 1 | a0001c0001t0003g0195 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.2566-14761C>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57651707 | ||||||
chr13:57651837
|
ATAT | A | 4 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0034g0247others(1): Show | 4 | HG02257.hp2 HG03098.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.2566-14623_2566-14 others(9): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 57651837 | |||||
chr13:57651954
|
A | G | 1 | a0001c0001t0002g0093 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2566-14514A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57651954 | ||||||
chr13:57652033
|
C | G | 2 | a0001c0001t0034g0247a0001c0001t0035g0063 | 2 | HG02257.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.2566-14435C>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57652033 | ||||||
chr13:57652207
|
A | G | 1 | a0001c0001t0007g0116 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.2566-14261A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57652207 | ||||||
chr13:57652284
|
C | CA | 59 | a0001c0001t0001g0002a0001c0001t0001g0059a0001c0001t0001g0103others(56): Show | 59 | HG00323.hp1 HG01081.hp2 HG01099.hp2 others(56): Show |
intron_variant | MODIFIER | c.2566-14166dupA | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 57652284 | |||||
chr13:57652284
|
C | CAA | 165 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(162): Show | 169 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(166): Show |
intron_variant | MODIFIER | c.2566-14167_2566-14 others(8): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 57652284 | |||||
chr13:57652284
|
C | CAAA | 15 | a0001c0001t0001g0170a0001c0001t0001g0175a0001c0001t0001g0189others(12): Show | 15 | HG01109.hp2 HG01175.hp1 HG01175.hp2 others(12): Show |
intron_variant | MODIFIER | c.2566-14168_2566-14 others(9): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 57652284 | |||||
chr13:57652567
|
C | A | 1 | a0001c0001t0001g0059 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2566-13901C>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57652567 | ||||||
chr13:57652610
|
A | G | 18 | a0001c0001t0001g0010a0001c0001t0001g0065a0001c0001t0001g0066others(15): Show | 18 | HG00639.hp2 HG01106.hp1 HG01256.hp2 others(15): Show |
intron_variant | MODIFIER | c.2566-13858A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57652610 | ||||||
chr13:57652766
|
G | A | 2 | a0001c0001t0002g0008a0001c0001t0002g0009 | 2 | HG03130.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.2566-13702G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57652766 | ||||||
chr13:57652785
|
A | G | 1 | a0001c0001t0035g0063 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2566-13683A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57652785 | ||||||
chr13:57652808
|
G | A | 52 | a0001c0001t0001g0002a0001c0001t0001g0103a0001c0001t0001g0110others(49): Show | 52 | HG00323.hp1 HG01081.hp2 HG01099.hp2 others(49): Show |
intron_variant | MODIFIER | c.2566-13660G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57652808 | ||||||
chr13:57652913
|
C | G | 1 | a0001c0001t0002g0120 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.2566-13555C>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57652913 | ||||||
chr13:57652989
|
A | G | 26 | a0001c0001t0001g0127a0001c0001t0001g0139a0001c0001t0002g0128others(23): Show | 26 | HG01243.hp1 HG01884.hp2 HG01891.hp1 others(23): Show |
intron_variant | MODIFIER | c.2566-13479A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57652989 | ||||||
chr13:57653157
|
T | A | 18 | a0001c0001t0001g0010a0001c0001t0001g0065a0001c0001t0001g0066others(15): Show | 18 | HG00639.hp2 HG01106.hp1 HG01256.hp2 others(15): Show |
intron_variant | MODIFIER | c.2566-13311T>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57653157 | ||||||
chr13:57653325
|
AC | A | 3 | a0001c0001t0018g0060a0001c0004t0005g0061a0001c0004t0005g0062 | 3 | HG02055.hp2 HG02257.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.2566-13141delC | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 57653325 | |||||
chr13:57653441
|
A | G | 1 | a0001c0001t0006g0096 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.2566-13027A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57653441 | ||||||
chr13:57653442
|
T | C | 1 | a0001c0001t0004g0137 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.2566-13026T>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57653442 | ||||||
chr13:57653611
|
G | A | 5 | a0001c0001t0002g0270a0001c0001t0003g0268a0001c0001t0003g0296others(2): Show | 5 | HG01109.hp2 HG01361.hp2 HG03239.hp1 others(2): Show |
intron_variant | MODIFIER | c.2566-12857G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57653611 | ||||||
chr13:57653618
|
G | T | 1 | a0001c0001t0011g0021 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.2566-12850G>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57653618 | ||||||
chr13:57654202
|
A | T | 164 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0059others(161): Show | 168 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(165): Show |
intron_variant | MODIFIER | c.2566-12266A>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57654202 | ||||||
chr13:57654319
|
A | G | 1 | a0001c0001t0001g0155 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2566-12149A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57654319 | ||||||
chr13:57654361
|
A | G | 10 | a0001c0001t0001g0257a0001c0001t0002g0205a0001c0001t0002g0251others(7): Show | 10 | HG00544.hp1 HG00597.hp1 NA18945.hp2 others(7): Show |
intron_variant | MODIFIER | c.2566-12107A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57654361 | ||||||
chr13:57654401
|
GT | G | 30 | a0001c0001t0001g0127a0001c0001t0001g0139a0001c0001t0002g0128others(27): Show | 30 | HG01243.hp1 HG01884.hp2 HG01891.hp1 others(27): Show |
intron_variant | MODIFIER | c.2566-12057delT | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 57654401 | |||||
chr13:57654401
|
GTT | G | 26 | a0001c0001t0001g0002a0001c0001t0001g0103a0001c0001t0001g0110others(23): Show | 26 | HG00323.hp1 HG01081.hp2 HG01099.hp2 others(23): Show |
intron_variant | MODIFIER | c.2566-12058_2566-12 others(8): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 57654401 | |||||
chr13:57654660
|
C | T | 19 | a0001c0001t0001g0010a0001c0001t0001g0065a0001c0001t0001g0066others(16): Show | 19 | HG00639.hp2 HG01106.hp1 HG01256.hp2 others(16): Show |
intron_variant | MODIFIER | c.2566-11808C>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57654660 | ||||||
chr13:57654936
|
T | C | 237 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(234): Show | 241 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(238): Show |
intron_variant | MODIFIER | c.2566-11532T>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57654936 | ||||||
chr13:57654982
|
GTTGGGGA others(9): Show |
G | 1 | a0001c0001t0017g0224 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.2566-11483_2566-11 others(22): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 57654982 | |||||
chr13:57655211
|
G | GC | 218 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(215): Show | 222 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(219): Show |
intron_variant | MODIFIER | c.2566-11257_2566-11 others(7): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57655211 | ||||||
chr13:57655426
|
A | G | 2 | a0001c0001t0034g0247a0001c0001t0035g0063 | 2 | HG02257.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.2566-11042A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57655426 | ||||||
chr13:57655826
|
G | A | 1 | a0001c0001t0023g0176 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.2566-10642G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57655826 | ||||||
chr13:57655868
|
T | TA | 257 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(254): Show | 261 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(258): Show |
intron_variant | MODIFIER | c.2566-10593dupA | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 57655868 | |||||
chr13:57656079
|
GA | G | 55 | a0001c0001t0001g0007a0001c0001t0001g0238a0001c0001t0001g0257others(52): Show | 55 | HG00280.hp1 HG00544.hp1 HG00597.hp1 others(52): Show |
intron_variant | MODIFIER | c.2566-10381delA | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 57656079 | |||||
chr13:57656089
|
G | A | 55 | a0001c0001t0001g0007a0001c0001t0001g0238a0001c0001t0001g0257others(52): Show | 55 | HG00280.hp1 HG00544.hp1 HG00597.hp1 others(52): Show |
intron_variant | MODIFIER | c.2566-10379G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57656089 | ||||||
chr13:57656347
|
G | A | 1 | a0001c0001t0034g0247 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2566-10121G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57656347 | ||||||
chr13:57656440
|
T | C | 52 | a0001c0001t0001g0002a0001c0001t0001g0103a0001c0001t0001g0110others(49): Show | 52 | HG00323.hp1 HG01081.hp2 HG01099.hp2 others(49): Show |
intron_variant | MODIFIER | c.2566-10028T>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57656440 | ||||||
chr13:57656562
|
G | A | 1 | a0004c0015t0003g0032 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.2566-9906G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57656562 | ||||||
chr13:57656890
|
A | C | 164 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0059others(161): Show | 168 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(165): Show |
intron_variant | MODIFIER | c.2566-9578A>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57656890 | ||||||
chr13:57657139
|
G | A | 2 | a0001c0001t0001g0189a0001c0001t0002g0198 | 2 | NA19002.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.2566-9329G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57657139 | ||||||
chr13:57657185
|
A | C | 2 | a0001c0001t0034g0247a0001c0001t0035g0063 | 2 | HG02257.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.2566-9283A>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57657185 | ||||||
chr13:57657452
|
A | T | 1 | a0001c0001t0034g0247 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2566-9016A>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57657452 | ||||||
chr13:57657470
|
TTA | T | 4 | a0001c0001t0001g0059a0001c0001t0018g0060a0001c0004t0005g0061others(1): Show | 4 | HG02055.hp2 HG02257.hp1 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.2566-8996_2566-899 others(6): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 57657470 | |||||
chr13:57657524
|
A | G | 1 | a0001c0001t0002g0093 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2566-8944A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57657524 | ||||||
chr13:57657642
|
T | C | 1 | a0001c0001t0017g0152 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.2566-8826T>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57657642 | ||||||
chr13:57657678
|
G | C | 2 | a0001c0001t0001g0127a0001c0001t0002g0128 | 2 | HG02486.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.2566-8790G>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57657678 | ||||||
chr13:57657811
|
T | G | 3 | a0001c0001t0006g0058a0001c0001t0008g0001a0001c0001t0008g0017 | 4 | HG02148.hp2 NA18949.hp2 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.2566-8657T>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57657811 | ||||||
chr13:57658300
|
G | A | 1 | a0001c0005t0028g0052 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.2566-8168G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57658300 | ||||||
chr13:57658355
|
G | C | 3 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0021g0074 | 3 | HG02735.hp1 HG03017.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.2566-8113G>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57658355 | ||||||
chr13:57658426
|
C | A | 1 | a0001c0001t0002g0009 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2566-8042C>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57658426 | ||||||
chr13:57658640
|
G | A | 26 | a0001c0001t0001g0002a0001c0001t0001g0103a0001c0001t0001g0110others(23): Show | 26 | HG00323.hp1 HG01081.hp2 HG01099.hp2 others(23): Show |
intron_variant | MODIFIER | c.2566-7828G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57658640 | ||||||
chr13:57658764
|
G | GTTTGT | 26 | a0001c0001t0001g0002a0001c0001t0001g0059a0001c0001t0001g0101others(23): Show | 26 | HG00597.hp1 HG01109.hp1 HG01255.hp1 others(23): Show |
intron_variant | MODIFIER | c.2566-7674_2566-767 others(9): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 57658764 | |||||
chr13:57658764
|
G | GTTTGTTT others(3): Show |
4 | a0001c0001t0001g0103a0001c0001t0001g0115a0001c0001t0005g0122others(1): Show | 4 | HG02257.hp2 HG02280.hp2 NA18982.hp2 others(1): Show |
intron_variant | MODIFIER | c.2566-7679_2566-767 others(14): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 57658764 | |||||
chr13:57658764
|
G | GTTTGTTT others(8): Show |
38 | a0001c0001t0001g0110a0001c0001t0001g0118a0001c0001t0001g0119others(35): Show | 38 | HG00323.hp1 HG01081.hp2 HG01099.hp2 others(35): Show |
intron_variant | MODIFIER | c.2566-7684_2566-767 others(19): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 57658764 | |||||
chr13:57658764
|
G | GTTTGTTT others(13): Show |
8 | a0001c0001t0001g0139a0001c0001t0002g0138a0001c0001t0002g0141others(5): Show | 8 | HG01243.hp1 HG01975.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.2566-7689_2566-767 others(24): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 57658764 | |||||
chr13:57658764
|
G | GTTTGTTT others(18): Show |
1 | a0001c0001t0004g0117 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.2566-7694_2566-767 others(29): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 57658764 | |||||
chr13:57658883
|
G | A | 1 | a0001c0001t0018g0060 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2566-7585G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57658883 | ||||||
chr13:57658911
|
C | T | 1 | a0001c0001t0003g0073 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.2566-7557C>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57658911 | ||||||
chr13:57659021
|
A | T | 2 | a0001c0004t0005g0061a0001c0004t0005g0062 | 2 | HG02257.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.2566-7447A>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57659021 | ||||||
chr13:57659103
|
T | TTG | 13 | a0001c0001t0001g0059a0001c0001t0002g0005a0001c0001t0002g0008others(10): Show | 14 | HG00741.hp2 HG01192.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.2566-7337_2566-733 others(6): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 57659103 | |||||
chr13:57659103
|
T | TTGTG | 11 | a0001c0001t0002g0009a0001c0001t0002g0068a0001c0001t0002g0216others(8): Show | 11 | HG00738.hp1 HG00741.hp1 HG01099.hp1 others(8): Show |
intron_variant | MODIFIER | c.2566-7339_2566-733 others(8): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 57659103 | |||||
chr13:57659103
|
T | TTGTGTG | 70 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0079others(67): Show | 73 | HG00323.hp2 HG00544.hp2 HG00558.hp1 others(70): Show |
intron_variant | MODIFIER | c.2566-7341_2566-733 others(10): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 57659103 | |||||
chr13:57659103
|
T | TTGTGTGT others(1): Show |
40 | a0001c0001t0001g0065a0001c0001t0001g0066a0001c0001t0001g0076others(37): Show | 40 | HG00140.hp1 HG00140.hp2 HG00621.hp1 others(37): Show |
intron_variant | MODIFIER | c.2566-7343_2566-733 others(12): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 57659103 | |||||
chr13:57659103
|
T | TTGTGTGT others(3): Show |
39 | a0001c0001t0001g0007a0001c0001t0001g0238a0001c0001t0001g0257others(36): Show | 39 | HG00280.hp1 HG00544.hp1 HG00597.hp1 others(36): Show |
intron_variant | MODIFIER | c.2566-7345_2566-733 others(14): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 57659103 | |||||
chr13:57659103
|
T | TTGTGTGT others(5): Show |
2 | a0001c0001t0022g0292a0001c0001t0048g0289 | 2 | NA18971.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.2566-7347_2566-733 others(16): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 57659103 | |||||
chr13:57659103
|
T | TTGTGTGT others(7): Show |
1 | a0001c0001t0003g0296 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.2566-7349_2566-733 others(18): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 57659103 | |||||
chr13:57659103
|
TTG | T | 4 | a0001c0001t0002g0086a0001c0001t0002g0270a0001c0001t0011g0021others(1): Show | 4 | HG01109.hp1 HG03239.hp1 NA18982.hp1 others(1): Show |
intron_variant | MODIFIER | c.2566-7337_2566-733 others(6): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 57659103 | |||||
chr13:57659103
|
TTGTGTG | T | 4 | a0001c0001t0015g0013a0001c0001t0015g0014a0001c0001t0015g0015others(1): Show | 4 | HG02572.hp2 HG02615.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.2566-7341_2566-733 others(10): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 57659103 | |||||
chr13:57659131
|
G | A | 1 | a0001c0001t0004g0303 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2566-7337G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57659131 | ||||||
chr13:57659131
|
G | GTA | 7 | a0001c0001t0001g0139a0001c0001t0002g0138a0001c0001t0002g0141others(4): Show | 7 | HG02723.hp1 HG02809.hp2 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.2566-7334_2566-733 others(6): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 57659131 | |||||
chr13:57659131
|
G | GTGTA | 40 | a0001c0001t0001g0002a0001c0001t0001g0103a0001c0001t0001g0110others(37): Show | 40 | HG00323.hp1 HG01081.hp2 HG01099.hp2 others(37): Show |
intron_variant | MODIFIER | c.2566-7336_2566-733 others(8): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 57659131 | |||||
chr13:57659131
|
G | GTGTGTA | 4 | a0001c0001t0001g0127a0001c0001t0002g0102a0001c0001t0002g0128others(1): Show | 4 | HG02280.hp1 HG02486.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.2566-7336_2566-733 others(10): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 57659131 | |||||
chr13:57659167
|
A | G | 21 | a0001c0001t0001g0101a0001c0001t0002g0080a0001c0001t0002g0086others(18): Show | 21 | HG01109.hp1 HG01255.hp1 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.2566-7301A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57659167 | ||||||
chr13:57659188
|
T | C | 20 | a0001c0001t0001g0010a0001c0001t0001g0065a0001c0001t0001g0066others(17): Show | 20 | HG00140.hp2 HG00639.hp2 HG01106.hp1 others(17): Show |
intron_variant | MODIFIER | c.2566-7280T>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57659188 | ||||||
chr13:57659633
|
C | G | 2 | a0001c0001t0034g0247a0001c0001t0035g0063 | 2 | HG02257.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.2566-6835C>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57659633 | ||||||
chr13:57659897
|
G | A | 4 | a0001c0001t0001g0059a0001c0001t0018g0060a0001c0004t0005g0061others(1): Show | 4 | HG02055.hp2 HG02257.hp1 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.2566-6571G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57659897 | ||||||
chr13:57659961
|
G | A | 22 | a0001c0001t0001g0101a0001c0001t0002g0080a0001c0001t0002g0086others(19): Show | 22 | HG01109.hp1 HG01255.hp1 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.2566-6507G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57659961 | ||||||
chr13:57659961
|
G | C | 1 | a0001c0002t0049g0209 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2566-6507G>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57659961 | ||||||
chr13:57660030
|
C | T | 237 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(234): Show | 241 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(238): Show |
intron_variant | MODIFIER | c.2566-6438C>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57660030 | ||||||
chr13:57660092
|
A | C | 40 | a0001c0001t0001g0006a0001c0001t0001g0161a0001c0001t0001g0167others(37): Show | 42 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(39): Show |
intron_variant | MODIFIER | c.2566-6376A>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57660092 | ||||||
chr13:57660251
|
T | TA | 21 | a0001c0001t0001g0101a0001c0001t0002g0080a0001c0001t0002g0086others(18): Show | 21 | HG01109.hp1 HG01255.hp1 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.2566-6213dupA | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 57660251 | |||||
chr13:57660369
|
G | A | 1 | a0001c0001t0008g0017 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.2566-6099G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57660369 | ||||||
chr13:57660396
|
T | G | 1 | a0001c0001t0001g0059 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2566-6072T>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57660396 | ||||||
chr13:57661064
|
C | T | 1 | a0001c0001t0014g0196 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.2566-5404C>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57661064 | ||||||
chr13:57661065
|
G | A | 1 | a0001c0001t0001g0101 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.2566-5403G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57661065 | ||||||
chr13:57661069
|
G | A | 100 | a0001c0001t0001g0006a0001c0001t0001g0150a0001c0001t0001g0155others(97): Show | 104 | HG00140.hp1 HG00323.hp2 HG00544.hp2 others(101): Show |
intron_variant | MODIFIER | c.2566-5399G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57661069 | ||||||
chr13:57661368
|
T | C | 1 | a0001c0001t0002g0141 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2566-5100T>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57661368 | ||||||
chr13:57661466
|
T | C | 1 | a0001c0001t0039g0267 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2566-5002T>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57661466 | ||||||
chr13:57661579
|
T | A | 2 | a0001c0001t0002g0080a0001c0001t0053g0081 | 2 | NA18943.hp1 NA18985.hp2 |
intron_variant | MODIFIER | c.2566-4889T>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57661579 | ||||||
chr13:57661587
|
T | A | 54 | a0001c0001t0001g0002a0001c0001t0001g0103a0001c0001t0001g0110others(51): Show | 54 | HG00323.hp1 HG01081.hp2 HG01099.hp2 others(51): Show |
intron_variant | MODIFIER | c.2566-4881T>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57661587 | ||||||
chr13:57661658
|
A | G | 1 | a0001c0001t0003g0246 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.2566-4810A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57661658 | ||||||
chr13:57661812
|
C | T | 237 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(234): Show | 241 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(238): Show |
intron_variant | MODIFIER | c.2566-4656C>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57661812 | ||||||
chr13:57661845
|
G | A | 1 | a0001c0001t0001g0059 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2566-4623G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57661845 | ||||||
chr13:57661876
|
G | A | 53 | a0001c0001t0001g0007a0001c0001t0001g0238a0001c0001t0001g0257others(50): Show | 53 | HG00280.hp1 HG00544.hp1 HG00597.hp1 others(50): Show |
intron_variant | MODIFIER | c.2566-4592G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57661876 | ||||||
chr13:57661894
|
G | A | 1 | a0001c0001t0004g0303 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2566-4574G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57661894 | ||||||
chr13:57661903
|
T | C | 1 | a0001c0001t0004g0254 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.2566-4565T>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57661903 | ||||||
chr13:57661963
|
G | A | 21 | a0001c0001t0001g0101a0001c0001t0002g0080a0001c0001t0002g0086others(18): Show | 21 | HG01109.hp1 HG01255.hp1 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.2566-4505G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57661963 | ||||||
chr13:57662194
|
G | A | 1 | a0001c0001t0002g0102 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2566-4274G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57662194 | ||||||
chr13:57662359
|
A | G | 2 | a0001c0001t0002g0008a0001c0001t0002g0009 | 2 | HG03130.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.2566-4109A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57662359 | ||||||
chr13:57662574
|
CACAA | C | 53 | a0001c0001t0001g0007a0001c0001t0001g0238a0001c0001t0001g0257others(50): Show | 53 | HG00280.hp1 HG00544.hp1 HG00597.hp1 others(50): Show |
intron_variant | MODIFIER | c.2566-3890_2566-388 others(8): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 57662574 | |||||
chr13:57662761
|
A | G | 108 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0150others(105): Show | 112 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(109): Show |
intron_variant | MODIFIER | c.2566-3707A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57662761 | ||||||
chr13:57662878
|
T | C | 3 | a0001c0001t0003g0151a0001c0001t0003g0220a0005c0014t0006g0160 | 3 | HG00323.hp2 HG01069.hp2 HG01934.hp2 |
intron_variant | MODIFIER | c.2566-3590T>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57662878 | ||||||
chr13:57662960
|
C | T | 237 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(234): Show | 241 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(238): Show |
intron_variant | MODIFIER | c.2566-3508C>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57662960 | ||||||
chr13:57663002
|
A | T | 2 | a0001c0001t0002g0008a0001c0001t0002g0009 | 2 | HG03130.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.2566-3466A>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57663002 | ||||||
chr13:57663101
|
A | T | 1 | a0001c0001t0029g0051 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.2566-3367A>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57663101 | ||||||
chr13:57663381
|
G | A | 19 | a0001c0001t0001g0010a0001c0001t0001g0065a0001c0001t0001g0066others(16): Show | 19 | HG00639.hp2 HG01106.hp1 HG01256.hp2 others(16): Show |
intron_variant | MODIFIER | c.2566-3087G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57663381 | ||||||
chr13:57663517
|
T | C | 4 | a0001c0001t0001g0059a0001c0001t0018g0060a0001c0004t0005g0061others(1): Show | 4 | HG02055.hp2 HG02257.hp1 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.2566-2951T>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57663517 | ||||||
chr13:57663605
|
G | A | 1 | a0001c0001t0013g0046 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2566-2863G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57663605 | ||||||
chr13:57663963
|
G | T | 1 | a0001c0001t0052g0154 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.2566-2505G>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57663963 | ||||||
chr13:57664087
|
A | G | 1 | a0001c0001t0011g0300 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.2566-2381A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57664087 | ||||||
chr13:57664283
|
C | G | 54 | a0001c0001t0001g0007a0001c0001t0001g0238a0001c0001t0001g0257others(51): Show | 54 | HG00280.hp1 HG00544.hp1 HG00597.hp1 others(51): Show |
intron_variant | MODIFIER | c.2566-2185C>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57664283 | ||||||
chr13:57664325
|
A | G | 1 | a0001c0003t0002g0287 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.2566-2143A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57664325 | ||||||
chr13:57664408
|
C | G | 1 | a0001c0003t0002g0287 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.2566-2060C>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57664408 | ||||||
chr13:57664411
|
A | G | 1 | a0001c0001t0022g0207 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.2566-2057A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57664411 | ||||||
chr13:57664726
|
A | G | 57 | a0001c0001t0001g0002a0001c0001t0001g0103a0001c0001t0001g0110others(54): Show | 57 | HG00323.hp1 HG01081.hp2 HG01099.hp2 others(54): Show |
intron_variant | MODIFIER | c.2566-1742A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57664726 | ||||||
chr13:57664818
|
A | T | 1 | a0001c0001t0006g0096 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.2566-1650A>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57664818 | ||||||
chr13:57664965
|
T | C | 1 | a0001c0001t0010g0237 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.2566-1503T>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57664965 | ||||||
chr13:57665113
|
G | A | 1 | a0001c0001t0001g0213 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.2566-1355G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57665113 | ||||||
chr13:57665146
|
A | T | 2 | a0001c0001t0012g0031a0001c0001t0012g0036 | 2 | NA18942.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.2566-1322A>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57665146 | ||||||
chr13:57665172
|
T | TG | 48 | a0001c0001t0001g0002a0001c0001t0001g0103a0001c0001t0001g0110others(45): Show | 48 | HG00323.hp1 HG01081.hp2 HG01099.hp2 others(45): Show |
intron_variant | MODIFIER | c.2566-1288dupG | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 57665172 | |||||
chr13:57665206
|
C | CACTT | 219 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(216): Show | 223 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.2566-1260_2566-125 others(8): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 57665206 | |||||
chr13:57665265
|
G | GA | 261 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(258): Show | 265 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(262): Show |
intron_variant | MODIFIER | c.2566-1203_2566-120 others(5): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57665265 | ||||||
chr13:57665339
|
C | T | 1 | a0001c0001t0018g0203 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2566-1129C>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57665339 | ||||||
chr13:57665555
|
C | T | 53 | a0001c0001t0001g0007a0001c0001t0001g0238a0001c0001t0001g0257others(50): Show | 53 | HG00280.hp1 HG00544.hp1 HG00597.hp1 others(50): Show |
intron_variant | MODIFIER | c.2566-913C>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57665555 | ||||||
chr13:57665762
|
A | G | 5 | a0001c0001t0036g0211a0001c0002t0001g0163a0001c0002t0005g0208others(2): Show | 5 | HG02486.hp1 HG02723.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.2566-706A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57665762 | ||||||
chr13:57665879
|
G | C | 219 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(216): Show | 223 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.2566-589G>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57665879 | ||||||
chr13:57667052
|
C | T | 238 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(235): Show | 242 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.2797+219C>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57667052 | ||||||
chr13:57667086
|
T | C | 19 | a0001c0001t0001g0010a0001c0001t0001g0065a0001c0001t0001g0066others(16): Show | 19 | HG00140.hp2 HG00639.hp2 HG01106.hp1 others(16): Show |
intron_variant | MODIFIER | c.2797+253T>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57667086 | ||||||
chr13:57667108
|
T | C | 1 | a0001c0001t0004g0111 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.2797+275T>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57667108 | ||||||
chr13:57667514
|
A | G | 2 | a0001c0001t0034g0247a0001c0001t0035g0063 | 2 | HG02257.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.2797+681A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57667514 | ||||||
chr13:57667554
|
G | A | 1 | a0001c0001t0002g0098 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.2797+721G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57667554 | ||||||
chr13:57667687
|
A | G | 1 | a0001c0001t0001g0103 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.2797+854A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57667687 | ||||||
chr13:57667769
|
TTA | T | 259 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(256): Show | 263 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(260): Show |
intron_variant | MODIFIER | c.2797+945_2797+946d others(4): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr13 | 57667769 | |||||
chr13:57667812
|
G | A | 1 | a0001c0001t0002g0234 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2797+979G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57667812 | ||||||
chr13:57667880
|
CTTAT | C | 97 | a0001c0001t0001g0006a0001c0001t0001g0150a0001c0001t0001g0155others(94): Show | 101 | HG00140.hp1 HG00323.hp2 HG00544.hp2 others(98): Show |
intron_variant | MODIFIER | c.2797+1052_2797+105 others(8): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr13 | 57667880 | |||||
chr13:57667895
|
T | A | 2 | a0001c0001t0002g0097a0001c0001t0008g0035 | 2 | HG02809.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.2797+1062T>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57667895 | ||||||
chr13:57667900
|
A | T | 1 | a0001c0001t0013g0027 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.2797+1067A>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57667900 | ||||||
chr13:57668022
|
G | C | 1 | a0001c0001t0001g0059 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2797+1189G>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57668022 | ||||||
chr13:57668167
|
G | T | 1 | a0001c0001t0013g0046 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2797+1334G>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57668167 | ||||||
chr13:57668331
|
G | A | 1 | a0001c0001t0003g0226 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.2797+1498G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57668331 | ||||||
chr13:57668404
|
T | C | 28 | a0001c0001t0001g0002a0001c0001t0001g0103a0001c0001t0001g0110others(25): Show | 28 | HG00323.hp1 HG01081.hp2 HG01099.hp2 others(25): Show |
intron_variant | MODIFIER | c.2797+1571T>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57668404 | ||||||
chr13:57668566
|
A | T | 217 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(214): Show | 221 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(218): Show |
intron_variant | MODIFIER | c.2797+1733A>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57668566 | ||||||
chr13:57668801
|
A | G | 1 | a0001c0001t0002g0135 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2797+1968A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57668801 | ||||||
chr13:57668998
|
C | T | 1 | a0001c0001t0002g0009 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2797+2165C>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57668998 | ||||||
chr13:57669016
|
G | A | 2 | a0001c0001t0002g0089a0001c0001t0002g0091 | 2 | HG02630.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.2797+2183G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57669016 | ||||||
chr13:57669388
|
T | C | 1 | a0001c0001t0044g0230 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2797+2555T>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57669388 | ||||||
chr13:57669434
|
G | A | 267 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(264): Show | 271 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(268): Show |
intron_variant | MODIFIER | c.2797+2601G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57669434 | ||||||
chr13:57669753
|
A | G | 1 | a0001c0001t0002g0097 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2797+2920A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57669753 | ||||||
chr13:57670332
|
C | T | 4 | a0001c0001t0001g0059a0001c0001t0018g0060a0001c0004t0005g0061others(1): Show | 4 | HG02055.hp2 HG02257.hp1 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.2797+3499C>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57670332 | ||||||
chr13:57670350
|
T | C | 1 | a0001c0001t0007g0187 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.2797+3517T>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57670350 | ||||||
chr13:57670745
|
T | C | 1 | a0001c0001t0002g0102 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2797+3912T>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57670745 | ||||||
chr13:57670869
|
G | A | 1 | a0001c0001t0002g0225 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.2797+4036G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57670869 | ||||||
chr13:57671007
|
G | T | 1 | a0001c0001t0002g0301 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2797+4174G>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57671007 | ||||||
chr13:57671017
|
C | A | 150 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0150others(147): Show | 154 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(151): Show |
intron_variant | MODIFIER | c.2797+4184C>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57671017 | ||||||
chr13:57671041
|
C | G | 4 | a0001c0001t0001g0059a0001c0001t0018g0060a0001c0004t0005g0061others(1): Show | 4 | HG02055.hp2 HG02257.hp1 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.2797+4208C>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57671041 | ||||||
chr13:57671048
|
T | C | 1 | a0001c0001t0001g0049 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.2797+4215T>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57671048 | ||||||
chr13:57671087
|
C | G | 28 | a0001c0001t0001g0002a0001c0001t0001g0103a0001c0001t0001g0110others(25): Show | 28 | HG00323.hp1 HG01081.hp2 HG01099.hp2 others(25): Show |
intron_variant | MODIFIER | c.2797+4254C>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57671087 | ||||||
chr13:57671267
|
T | C | 55 | a0001c0001t0001g0002a0001c0001t0001g0103a0001c0001t0001g0110others(52): Show | 55 | HG00323.hp1 HG01081.hp2 HG01099.hp2 others(52): Show |
intron_variant | MODIFIER | c.2797+4434T>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57671267 | ||||||
chr13:57671394
|
A | G | 2 | a0001c0001t0002g0008a0001c0001t0002g0009 | 2 | HG03130.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.2797+4561A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57671394 | ||||||
chr13:57671544
|
A | G | 55 | a0001c0001t0001g0002a0001c0001t0001g0103a0001c0001t0001g0110others(52): Show | 55 | HG00323.hp1 HG01081.hp2 HG01099.hp2 others(52): Show |
intron_variant | MODIFIER | c.2797+4711A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57671544 | ||||||
chr13:57671820
|
G | A | 4 | a0001c0001t0001g0059a0001c0001t0018g0060a0001c0004t0005g0061others(1): Show | 4 | HG02055.hp2 HG02257.hp1 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.2797+4987G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57671820 | ||||||
chr13:57671878
|
C | T | 261 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(258): Show | 265 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(262): Show |
intron_variant | MODIFIER | c.2797+5045C>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57671878 | ||||||
chr13:57672027
|
C | T | 2 | a0001c0001t0034g0247a0001c0001t0035g0063 | 2 | HG02257.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.2797+5194C>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57672027 | ||||||
chr13:57672028
|
T | G | 1 | a0001c0001t0007g0173 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.2797+5195T>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57672028 | ||||||
chr13:57672338
|
T | C | 1 | a0001c0001t0011g0047 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.2797+5505T>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57672338 | ||||||
chr13:57672346
|
G | A | 1 | a0001c0001t0007g0181 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.2797+5513G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57672346 | ||||||
chr13:57672670
|
C | T | 1 | a0001c0001t0018g0203 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2797+5837C>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57672670 | ||||||
chr13:57672846
|
G | A | 54 | a0001c0001t0001g0007a0001c0001t0001g0238a0001c0001t0001g0257others(51): Show | 54 | HG00280.hp1 HG00544.hp1 HG00597.hp1 others(51): Show |
intron_variant | MODIFIER | c.2797+6013G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57672846 | ||||||
chr13:57672868
|
A | G | 4 | a0001c0001t0015g0013a0001c0001t0015g0014a0001c0001t0015g0015others(1): Show | 4 | HG02572.hp2 HG02615.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.2797+6035A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57672868 | ||||||
chr13:57672909
|
T | C | 1 | a0001c0001t0002g0102 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2797+6076T>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57672909 | ||||||
chr13:57673140
|
G | T | 96 | a0001c0001t0001g0006a0001c0001t0001g0150a0001c0001t0001g0155others(93): Show | 100 | HG00140.hp1 HG00323.hp2 HG00544.hp2 others(97): Show |
intron_variant | MODIFIER | c.2797+6307G>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57673140 | ||||||
chr13:57673313
|
C | T | 1 | a0001c0001t0002g0093 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2797+6480C>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57673313 | ||||||
chr13:57673381
|
G | C | 2 | a0001c0001t0004g0199a0001c0011t0001g0214 | 2 | NA18992.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.2797+6548G>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57673381 | ||||||
chr13:57673502
|
C | T | 52 | a0001c0001t0001g0002a0001c0001t0001g0103a0001c0001t0001g0110others(49): Show | 52 | HG00323.hp1 HG01099.hp2 HG01123.hp1 others(49): Show |
intron_variant | MODIFIER | c.2797+6669C>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57673502 | ||||||
chr13:57673620
|
T | C | 22 | a0001c0001t0001g0101a0001c0001t0002g0080a0001c0001t0002g0086others(19): Show | 22 | HG01109.hp1 HG01255.hp1 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.2797+6787T>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57673620 | ||||||
chr13:57673710
|
G | T | 50 | a0001c0001t0001g0002a0001c0001t0001g0103a0001c0001t0001g0110others(47): Show | 50 | HG00323.hp1 HG01099.hp2 HG01123.hp1 others(47): Show |
intron_variant | MODIFIER | c.2797+6877G>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57673710 | ||||||
chr13:57673762
|
T | C | 1 | a0001c0001t0018g0060 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2797+6929T>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57673762 | ||||||
chr13:57673830
|
T | C | 54 | a0001c0001t0001g0238a0001c0001t0001g0257a0001c0001t0001g0258others(51): Show | 54 | HG00280.hp1 HG00544.hp1 HG00597.hp1 others(51): Show |
intron_variant | MODIFIER | c.2797+6997T>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57673830 | ||||||
chr13:57673883
|
ATCTCGGT others(8): Show |
A | 32 | a0001c0001t0001g0059a0001c0001t0001g0127a0001c0001t0001g0139others(29): Show | 32 | HG01243.hp1 HG01884.hp2 HG01891.hp1 others(29): Show |
intron_variant | MODIFIER | c.2797+7054_2797+706 others(19): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr13 | 57673883 | |||||
chr13:57673990
|
A | C | 144 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(141): Show | 148 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(145): Show |
intron_variant | MODIFIER | c.2797+7157A>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57673990 | ||||||
chr13:57674034
|
A | C | 1 | a0001c0001t0002g0225 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.2797+7201A>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57674034 | ||||||
chr13:57674288
|
G | A | 3 | a0001c0001t0015g0013a0001c0001t0015g0015a0001c0001t0037g0012 | 3 | HG02572.hp2 HG02615.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.2797+7455G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57674288 | ||||||
chr13:57674458
|
G | A | 7 | a0001c0001t0002g0089a0001c0001t0002g0091a0001c0001t0002g0098others(4): Show | 7 | HG01255.hp1 HG01891.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.2797+7625G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57674458 | ||||||
chr13:57674488
|
C | T | 1 | a0001c0003t0002g0287 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.2797+7655C>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57674488 | ||||||
chr13:57674598
|
G | A | 117 | a0001c0001t0001g0007a0001c0001t0001g0049a0001c0001t0001g0059others(114): Show | 119 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(116): Show |
intron_variant | MODIFIER | c.2797+7765G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57674598 | ||||||
chr13:57674655
|
C | T | 44 | a0001c0001t0001g0002a0001c0001t0001g0079a0001c0001t0001g0129others(41): Show | 44 | HG01099.hp2 HG01109.hp2 HG01175.hp2 others(41): Show |
intron_variant | MODIFIER | c.2797+7822C>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57674655 | ||||||
chr13:57674681
|
A | G | 1 | a0001c0012t0001g0094 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2797+7848A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57674681 | ||||||
chr13:57674903
|
G | A | 2 | a0001c0001t0007g0116a0001c0001t0054g0174 | 2 | HG00323.hp1 HG01081.hp1 |
intron_variant | MODIFIER | c.2797+8070G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57674903 | ||||||
chr13:57675293
|
C | T | 1 | a0001c0001t0002g0277 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2797+8460C>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57675293 | ||||||
chr13:57675296
|
A | G | 18 | a0001c0001t0002g0266a0001c0001t0006g0016a0001c0001t0006g0083others(15): Show | 18 | HG00140.hp2 HG01069.hp2 HG01106.hp2 others(15): Show |
intron_variant | MODIFIER | c.2797+8463A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57675296 | ||||||
chr13:57675339
|
A | G | 1 | a0001c0001t0004g0136 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2797+8506A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57675339 | ||||||
chr13:57675396
|
G | A | 2 | a0001c0001t0001g0186a0001c0001t0021g0183 | 2 | HG00738.hp2 HG01168.hp1 |
intron_variant | MODIFIER | c.2797+8563G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57675396 | ||||||
chr13:57675723
|
G | C | 18 | a0001c0001t0002g0266a0001c0001t0006g0016a0001c0001t0006g0083others(15): Show | 18 | HG00140.hp2 HG01069.hp2 HG01106.hp2 others(15): Show |
intron_variant | MODIFIER | c.2797+8890G>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57675723 | ||||||
chr13:57676086
|
AT | A | 3 | a0001c0001t0004g0177a0001c0001t0004g0215a0001c0005t0028g0052 | 3 | HG02083.hp1 HG02135.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.2797+9255delT | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr13 | 57676086 | |||||
chr13:57676100
|
T | C | 1 | a0001c0001t0001g0010 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.2797+9267T>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57676100 | ||||||
chr13:57676188
|
TG | T | 110 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(107): Show | 111 | HG00140.hp1 HG00280.hp1 HG00558.hp2 others(108): Show |
intron_variant | MODIFIER | c.2797+9357delG | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr13 | 57676188 | |||||
chr13:57676930
|
C | T | 1 | a0001c0012t0001g0094 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2797+10097C>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57676930 | ||||||
chr13:57677306
|
T | C | 2 | a0001c0001t0018g0060a0001c0001t0018g0203 | 2 | HG02055.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.2797+10473T>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57677306 | ||||||
chr13:57677461
|
C | A | 3 | a0001c0001t0024g0222a0001c0001t0026g0248a0007c0008t0045g0269 | 3 | NA18992.hp1 NA19004.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.2797+10628C>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57677461 | ||||||
chr13:57677575
|
G | A | 2 | a0001c0001t0002g0005a0001c0001t0003g0226 | 3 | HG00741.hp2 HG01192.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.2797+10742G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57677575 | ||||||
chr13:57677763
|
A | C | 2 | a0001c0001t0018g0060a0001c0001t0018g0203 | 2 | HG02055.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.2797+10930A>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57677763 | ||||||
chr13:57677853
|
C | T | 126 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(123): Show | 127 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(124): Show |
intron_variant | MODIFIER | c.2797+11020C>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57677853 | ||||||
chr13:57678144
|
C | CAT | 61 | a0001c0001t0002g0068a0001c0001t0002g0089a0001c0001t0002g0091others(58): Show | 61 | HG00544.hp1 HG00544.hp2 HG00597.hp1 others(58): Show |
intron_variant | MODIFIER | c.2797+11328_2797+11 others(8): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr13 | 57678144 | |||||
chr13:57678144
|
C | CATAT | 20 | a0001c0001t0002g0266a0001c0001t0006g0016a0001c0001t0006g0058others(17): Show | 20 | HG00140.hp2 HG01069.hp2 HG01106.hp2 others(17): Show |
intron_variant | MODIFIER | c.2797+11326_2797+11 others(10): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr13 | 57678144 | |||||
chr13:57678444
|
G | A | 1 | a0005c0014t0006g0160 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.2797+11611G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57678444 | ||||||
chr13:57678667
|
G | A | 262 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(259): Show | 266 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.2797+11834G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57678667 | ||||||
chr13:57678808
|
A | T | 1 | a0001c0001t0014g0196 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.2797+11975A>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57678808 | ||||||
chr13:57678823
|
T | A | 1 | a0001c0001t0025g0204 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.2797+11990T>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57678823 | ||||||
chr13:57678933
|
C | T | 2 | a0001c0001t0006g0083a0001c0001t0006g0084 | 2 | NA19010.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.2797+12100C>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57678933 | ||||||
chr13:57678935
|
T | A | 2 | a0001c0001t0006g0083a0001c0001t0006g0084 | 2 | NA19010.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.2797+12102T>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57678935 | ||||||
chr13:57679279
|
G | A | 1 | a0001c0001t0043g0087 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2797+12446G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57679279 | ||||||
chr13:57679283
|
A | G | 1 | a0001c0001t0002g0266 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2797+12450A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57679283 | ||||||
chr13:57679320
|
C | T | 1 | a0001c0001t0004g0085 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.2797+12487C>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57679320 | ||||||
chr13:57679360
|
CA | C | 200 | a0001c0001t0001g0007a0001c0001t0001g0059a0001c0001t0001g0065others(197): Show | 203 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(200): Show |
intron_variant | MODIFIER | c.2797+12539delA | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr13 | 57679360 | |||||
chr13:57679360
|
CAA | C | 43 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0010others(40): Show | 44 | HG00597.hp2 HG01074.hp2 HG01169.hp1 others(41): Show |
intron_variant | MODIFIER | c.2797+12538_2797+12 others(8): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr13 | 57679360 | |||||
chr13:57679487
|
A | G | 3 | a0001c0001t0004g0177a0001c0001t0004g0215a0001c0005t0028g0052 | 3 | HG02083.hp1 HG02135.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.2797+12654A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57679487 | ||||||
chr13:57679508
|
A | G | 1 | a0001c0001t0023g0176 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.2797+12675A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57679508 | ||||||
chr13:57679599
|
C | T | 2 | a0001c0001t0004g0177a0001c0005t0028g0052 | 2 | HG02083.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.2797+12766C>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57679599 | ||||||
chr13:57679733
|
T | A | 8 | a0001c0001t0001g0161a0001c0001t0003g0011a0001c0001t0007g0078others(5): Show | 8 | HG00323.hp1 HG00558.hp1 HG00735.hp1 others(5): Show |
intron_variant | MODIFIER | c.2797+12900T>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57679733 | ||||||
chr13:57679822
|
A | G | 2 | a0001c0001t0007g0180a0001c0001t0007g0181 | 2 | NA18998.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.2797+12989A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57679822 | ||||||
chr13:57679843
|
G | A | 1 | a0001c0001t0002g0266 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2797+13010G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57679843 | ||||||
chr13:57679962
|
T | G | 11 | a0001c0001t0001g0059a0001c0001t0001g0129a0001c0001t0004g0303others(8): Show | 11 | HG01943.hp2 HG02258.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.2797+13129T>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57679962 | ||||||
chr13:57680003
|
A | T | 1 | a0001c0001t0001g0170 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.2797+13170A>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57680003 | ||||||
chr13:57680139
|
C | CAT | 58 | a0001c0001t0002g0068a0001c0001t0002g0089a0001c0001t0002g0091others(55): Show | 58 | HG00140.hp2 HG00544.hp1 HG00544.hp2 others(55): Show |
intron_variant | MODIFIER | c.2797+13320_2797+13 others(8): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr13 | 57680139 | |||||
chr13:57680178
|
A | G | 3 | a0001c0001t0001g0139a0001c0001t0010g0090a0001c0001t0010g0274 | 3 | HG01255.hp1 HG03041.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.2797+13345A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57680178 | ||||||
chr13:57680206
|
A | G | 1 | a0001c0001t0022g0292 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2797+13373A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57680206 | ||||||
chr13:57680254
|
G | T | 1 | a0001c0003t0002g0297 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.2797+13421G>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57680254 | ||||||
chr13:57680446
|
G | A | 42 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0010others(39): Show | 43 | HG00597.hp2 HG01074.hp2 HG01169.hp1 others(40): Show |
intron_variant | MODIFIER | c.2797+13613G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57680446 | ||||||
chr13:57680496
|
T | C | 72 | a0001c0001t0002g0005a0001c0001t0002g0080a0001c0001t0002g0120others(69): Show | 75 | HG00673.hp2 HG00741.hp2 HG01069.hp2 others(72): Show |
intron_variant | MODIFIER | c.2797+13663T>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57680496 | ||||||
chr13:57680554
|
C | A | 8 | a0001c0001t0001g0161a0001c0001t0003g0011a0001c0001t0007g0078others(5): Show | 8 | HG00323.hp1 HG00558.hp1 HG00735.hp1 others(5): Show |
intron_variant | MODIFIER | c.2797+13721C>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57680554 | ||||||
chr13:57680561
|
A | G | 1 | a0001c0001t0040g0109 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2797+13728A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57680561 | ||||||
chr13:57680639
|
A | C | 58 | a0001c0001t0001g0007a0001c0001t0001g0065a0001c0001t0001g0066others(55): Show | 58 | HG00140.hp1 HG00280.hp1 HG00558.hp2 others(55): Show |
intron_variant | MODIFIER | c.2797+13806A>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57680639 | ||||||
chr13:57680767
|
A | T | 5 | a0001c0001t0002g0128a0001c0001t0002g0140a0001c0001t0037g0012others(2): Show | 5 | HG02257.hp1 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.2797+13934A>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57680767 | ||||||
chr13:57680975
|
T | A | 20 | a0001c0001t0002g0266a0001c0001t0006g0016a0001c0001t0006g0058others(17): Show | 20 | HG00140.hp2 HG01069.hp2 HG01106.hp2 others(17): Show |
intron_variant | MODIFIER | c.2797+14142T>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57680975 | ||||||
chr13:57681041
|
G | A | 2 | a0001c0001t0002g0240a0001c0001t0005g0291 | 2 | NA18988.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.2797+14208G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57681041 | ||||||
chr13:57681130
|
G | A | 1 | a0001c0001t0015g0014 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2797+14297G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57681130 | ||||||
chr13:57681870
|
G | A | 1 | a0001c0001t0003g0296 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.2797+15037G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57681870 | ||||||
chr13:57681944
|
G | A | 2 | a0001c0001t0005g0122a0001c0001t0005g0123 | 2 | HG02280.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.2797+15111G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57681944 | ||||||
chr13:57682257
|
G | A | 6 | a0001c0001t0002g0128a0001c0001t0002g0140a0001c0001t0037g0012others(3): Show | 6 | HG02257.hp1 HG02258.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.2797+15424G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57682257 | ||||||
chr13:57682346
|
A | G | 1 | a0001c0001t0001g0127 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2797+15513A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57682346 | ||||||
chr13:57682627
|
G | A | 1 | a0001c0001t0010g0237 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.2797+15794G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57682627 | ||||||
chr13:57682646
|
G | A | 2 | a0001c0001t0006g0105a0001c0001t0006g0168 | 2 | HG01978.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.2797+15813G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57682646 | ||||||
chr13:57682746
|
C | T | 3 | a0001c0001t0001g0139a0001c0001t0010g0090a0001c0001t0010g0274 | 3 | HG01255.hp1 HG03041.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.2797+15913C>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57682746 | ||||||
chr13:57682827
|
C | T | 1 | a0001c0001t0002g0144 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2797+15994C>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57682827 | ||||||
chr13:57682893
|
T | C | 19 | a0001c0001t0006g0016a0001c0001t0006g0058a0001c0001t0006g0083others(16): Show | 19 | HG00140.hp2 HG01069.hp2 HG01106.hp2 others(16): Show |
intron_variant | MODIFIER | c.2797+16060T>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57682893 | ||||||
chr13:57683031
|
C | T | 244 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(241): Show | 248 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(245): Show |
intron_variant | MODIFIER | c.2797+16198C>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57683031 | ||||||
chr13:57683131
|
A | G | 58 | a0001c0001t0002g0068a0001c0001t0002g0089a0001c0001t0002g0091others(55): Show | 58 | HG00544.hp1 HG00544.hp2 HG00597.hp1 others(55): Show |
intron_variant | MODIFIER | c.2797+16298A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57683131 | ||||||
chr13:57683180
|
A | G | 1 | a0001c0001t0001g0049 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.2797+16347A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57683180 | ||||||
chr13:57683281
|
A | G | 20 | a0001c0001t0002g0266a0001c0001t0006g0016a0001c0001t0006g0058others(17): Show | 20 | HG00140.hp2 HG01069.hp2 HG01106.hp2 others(17): Show |
intron_variant | MODIFIER | c.2797+16448A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57683281 | ||||||
chr13:57683293
|
C | T | 108 | a0001c0001t0002g0005a0001c0001t0002g0068a0001c0001t0002g0080others(105): Show | 111 | HG00544.hp1 HG00544.hp2 HG00597.hp1 others(108): Show |
intron_variant | MODIFIER | c.2797+16460C>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57683293 | ||||||
chr13:57683384
|
G | A | 1 | a0001c0001t0001g0191 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.2797+16551G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57683384 | ||||||
chr13:57683422
|
C | G | 19 | a0001c0001t0006g0016a0001c0001t0006g0058a0001c0001t0006g0083others(16): Show | 19 | HG00140.hp2 HG01069.hp2 HG01106.hp2 others(16): Show |
intron_variant | MODIFIER | c.2797+16589C>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57683422 | ||||||
chr13:57683533
|
T | A | 264 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(261): Show | 268 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(265): Show |
intron_variant | MODIFIER | c.2797+16700T>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57683533 | ||||||
chr13:57683645
|
C | T | 1 | a0001c0001t0043g0087 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2797+16812C>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57683645 | ||||||
chr13:57683686
|
C | T | 1 | a0001c0001t0001g0189 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.2797+16853C>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57683686 | ||||||
chr13:57683687
|
G | A | 6 | a0001c0001t0002g0128a0001c0001t0002g0140a0001c0001t0037g0012others(3): Show | 6 | HG02257.hp1 HG02258.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.2797+16854G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57683687 | ||||||
chr13:57683717
|
C | T | 1 | a0001c0001t0002g0008 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2797+16884C>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57683717 | ||||||
chr13:57683777
|
C | T | 19 | a0001c0001t0006g0016a0001c0001t0006g0058a0001c0001t0006g0083others(16): Show | 19 | HG00140.hp2 HG01069.hp2 HG01106.hp2 others(16): Show |
intron_variant | MODIFIER | c.2797+16944C>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57683777 | ||||||
chr13:57683823
|
C | T | 19 | a0001c0001t0006g0016a0001c0001t0006g0058a0001c0001t0006g0083others(16): Show | 19 | HG00140.hp2 HG01069.hp2 HG01106.hp2 others(16): Show |
intron_variant | MODIFIER | c.2797+16990C>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57683823 | ||||||
chr13:57683878
|
A | G | 1 | a0001c0001t0015g0014 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2797+17045A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57683878 | ||||||
chr13:57683960
|
G | A | 106 | a0001c0001t0002g0005a0001c0001t0002g0068a0001c0001t0002g0080others(103): Show | 109 | HG00544.hp1 HG00544.hp2 HG00597.hp1 others(106): Show |
intron_variant | MODIFIER | c.2797+17127G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57683960 | ||||||
chr13:57683962
|
A | C | 1 | a0001c0001t0006g0083 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.2797+17129A>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57683962 | ||||||
chr13:57683995
|
AG | A | 19 | a0001c0001t0006g0016a0001c0001t0006g0058a0001c0001t0006g0083others(16): Show | 19 | HG00140.hp2 HG01069.hp2 HG01106.hp2 others(16): Show |
intron_variant | MODIFIER | c.2797+17166delG | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr13 | 57683995 | |||||
chr13:57684014
|
G | A | 19 | a0001c0001t0006g0016a0001c0001t0006g0058a0001c0001t0006g0083others(16): Show | 19 | HG00140.hp2 HG01069.hp2 HG01106.hp2 others(16): Show |
intron_variant | MODIFIER | c.2797+17181G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57684014 | ||||||
chr13:57684086
|
C | T | 1 | a0001c0001t0036g0211 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2797+17253C>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57684086 | ||||||
chr13:57684333
|
A | T | 3 | a0001c0001t0002g0301a0001c0001t0041g0088a0001c0001t0043g0087 | 3 | HG02572.hp1 HG02897.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.2797+17500A>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57684333 | ||||||
chr13:57684335
|
C | A | 3 | a0001c0001t0002g0301a0001c0001t0041g0088a0001c0001t0043g0087 | 3 | HG02572.hp1 HG02897.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.2797+17502C>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57684335 | ||||||
chr13:57684566
|
A | G | 19 | a0001c0001t0006g0016a0001c0001t0006g0058a0001c0001t0006g0083others(16): Show | 19 | HG00140.hp2 HG01069.hp2 HG01106.hp2 others(16): Show |
intron_variant | MODIFIER | c.2797+17733A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57684566 | ||||||
chr13:57684638
|
T | G | 3 | a0001c0001t0004g0092a0001c0001t0005g0147a0001c0001t0042g0279 | 3 | HG01891.hp2 HG02451.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.2797+17805T>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57684638 | ||||||
chr13:57685084
|
G | C | 2 | a0001c0001t0002g0008a0001c0001t0002g0234 | 2 | HG01884.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.2797+18251G>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57685084 | ||||||
chr13:57685141
|
G | C | 1 | a0001c0001t0025g0204 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.2797+18308G>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57685141 | ||||||
chr13:57685358
|
C | A | 153 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(150): Show | 154 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(151): Show |
intron_variant | MODIFIER | c.2797+18525C>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57685358 | ||||||
chr13:57686031
|
G | A | 8 | a0001c0001t0001g0161a0001c0001t0003g0011a0001c0001t0007g0078others(5): Show | 8 | HG00323.hp1 HG00558.hp1 HG00735.hp1 others(5): Show |
intron_variant | MODIFIER | c.2797+19198G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57686031 | ||||||
chr13:57686090
|
G | GA | 37 | a0001c0001t0002g0068a0001c0001t0002g0106a0001c0001t0002g0112others(34): Show | 37 | HG00544.hp1 HG00544.hp2 HG00597.hp1 others(34): Show |
intron_variant | MODIFIER | c.2797+19267dupA | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr13 | 57686090 | |||||
chr13:57686145
|
A | G | 110 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(107): Show | 111 | HG00140.hp1 HG00280.hp1 HG00558.hp2 others(108): Show |
intron_variant | MODIFIER | c.2797+19312A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57686145 | ||||||
chr13:57686298
|
C | G | 8 | a0001c0001t0001g0059a0001c0001t0004g0303a0001c0001t0005g0122others(5): Show | 8 | HG02258.hp2 HG02280.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.2797+19465C>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57686298 | ||||||
chr13:57686302
|
C | T | 19 | a0001c0001t0006g0016a0001c0001t0006g0058a0001c0001t0006g0083others(16): Show | 19 | HG00140.hp2 HG01069.hp2 HG01106.hp2 others(16): Show |
intron_variant | MODIFIER | c.2797+19469C>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57686302 | ||||||
chr13:57686436
|
T | C | 1 | a0001c0001t0005g0124 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2797+19603T>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57686436 | ||||||
chr13:57686594
|
A | C | 3 | a0001c0001t0001g0139a0001c0001t0010g0090a0001c0001t0010g0274 | 3 | HG01255.hp1 HG03041.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.2797+19761A>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57686594 | ||||||
chr13:57686614
|
C | T | 2 | a0001c0001t0002g0008a0001c0001t0002g0234 | 2 | HG01884.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.2797+19781C>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57686614 | ||||||
chr13:57686707
|
A | G | 1 | a0006c0009t0007g0293 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.2797+19874A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57686707 | ||||||
chr13:57686896
|
G | A | 20 | a0001c0001t0002g0089a0001c0001t0002g0091a0001c0001t0002g0098others(17): Show | 20 | HG01496.hp1 HG01891.hp1 HG02280.hp1 others(17): Show |
intron_variant | MODIFIER | c.2797+20063G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57686896 | ||||||
chr13:57686957
|
G | A | 1 | a0001c0001t0003g0296 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.2797+20124G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57686957 | ||||||
chr13:57687070
|
A | G | 2 | a0001c0001t0018g0060a0001c0001t0018g0203 | 2 | HG02055.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.2797+20237A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57687070 | ||||||
chr13:57687109
|
C | T | 5 | a0001c0001t0006g0058a0001c0001t0006g0096a0001c0001t0006g0100others(2): Show | 5 | NA18948.hp2 NA18959.hp2 NA18980.hp2 others(2): Show |
intron_variant | MODIFIER | c.2797+20276C>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57687109 | ||||||
chr13:57687431
|
A | G | 1 | a0001c0001t0008g0024 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.2797+20598A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57687431 | ||||||
chr13:57687525
|
T | C | 1 | a0004c0015t0003g0032 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.2797+20692T>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57687525 | ||||||
chr13:57687551
|
T | A | 2 | a0001c0001t0007g0180a0001c0001t0007g0181 | 2 | NA18998.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.2797+20718T>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57687551 | ||||||
chr13:57687783
|
A | G | 264 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(261): Show | 268 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(265): Show |
intron_variant | MODIFIER | c.2797+20950A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57687783 | ||||||
chr13:57687833
|
T | C | 5 | a0001c0001t0013g0046a0001c0001t0034g0247a0001c0001t0036g0211others(2): Show | 5 | HG02257.hp2 HG02486.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.2797+21000T>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57687833 | ||||||
chr13:57687872
|
A | T | 2 | a0001c0001t0002g0008a0001c0001t0002g0234 | 2 | HG01884.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.2797+21039A>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57687872 | ||||||
chr13:57687888
|
G | C | 1 | a0001c0001t0002g0145 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2797+21055G>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57687888 | ||||||
chr13:57687892
|
C | T | 2 | a0001c0001t0018g0060a0001c0001t0018g0203 | 2 | HG02055.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.2797+21059C>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57687892 | ||||||
chr13:57687942
|
C | G | 2 | a0001c0001t0002g0008a0001c0001t0002g0234 | 2 | HG01884.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.2797+21109C>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57687942 | ||||||
chr13:57687956
|
T | C | 18 | a0001c0001t0001g0161a0001c0001t0002g0008a0001c0001t0002g0009others(15): Show | 18 | HG00323.hp1 HG00558.hp1 HG00735.hp1 others(15): Show |
intron_variant | MODIFIER | c.2797+21123T>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57687956 | ||||||
chr13:57687982
|
G | C | 6 | a0001c0001t0002g0128a0001c0001t0002g0140a0001c0001t0037g0012others(3): Show | 6 | HG02257.hp1 HG02258.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.2797+21149G>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57687982 | ||||||
chr13:57688182
|
C | G | 2 | a0001c0001t0018g0060a0001c0001t0018g0203 | 2 | HG02055.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.2797+21349C>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57688182 | ||||||
chr13:57688351
|
T | C | 1 | a0001c0001t0030g0039 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.2797+21518T>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57688351 | ||||||
chr13:57688505
|
C | A | 2 | a0001c0001t0018g0060a0001c0001t0018g0203 | 2 | HG02055.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.2797+21672C>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57688505 | ||||||
chr13:57688811
|
A | G | 20 | a0001c0001t0002g0266a0001c0001t0006g0016a0001c0001t0006g0058others(17): Show | 20 | HG00140.hp2 HG01069.hp2 HG01106.hp2 others(17): Show |
intron_variant | MODIFIER | c.2797+21978A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57688811 | ||||||
chr13:57688860
|
A | G | 9 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0086others(6): Show | 9 | HG01109.hp1 HG01884.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.2797+22027A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57688860 | ||||||
chr13:57688879
|
A | G | 5 | a0001c0001t0002g0128a0001c0001t0002g0140a0001c0001t0037g0012others(2): Show | 5 | HG02257.hp1 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.2797+22046A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57688879 | ||||||
chr13:57689013
|
A | T | 1 | a0001c0001t0001g0157 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.2797+22180A>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57689013 | ||||||
chr13:57689056
|
G | C | 52 | a0001c0001t0002g0005a0001c0001t0002g0080a0001c0001t0002g0120others(49): Show | 55 | HG00673.hp2 HG00741.hp2 HG01081.hp2 others(52): Show |
intron_variant | MODIFIER | c.2797+22223G>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57689056 | ||||||
chr13:57689063
|
C | T | 1 | a0001c0001t0016g0286 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.2797+22230C>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57689063 | ||||||
chr13:57689070
|
T | G | 1 | a0001c0001t0010g0237 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.2797+22237T>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57689070 | ||||||
chr13:57689156
|
A | G | 89 | a0001c0001t0002g0005a0001c0001t0002g0068a0001c0001t0002g0080others(86): Show | 92 | HG00544.hp1 HG00544.hp2 HG00597.hp1 others(89): Show |
intron_variant | MODIFIER | c.2797+22323A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57689156 | ||||||
chr13:57689200
|
A | C | 1 | a0001c0001t0056g0056 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.2797+22367A>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57689200 | ||||||
chr13:57689328
|
G | A | 52 | a0001c0001t0002g0005a0001c0001t0002g0080a0001c0001t0002g0120others(49): Show | 55 | HG00673.hp2 HG00741.hp2 HG01081.hp2 others(52): Show |
intron_variant | MODIFIER | c.2797+22495G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57689328 | ||||||
chr13:57689357
|
C | T | 1 | a0001c0001t0002g0234 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2797+22524C>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57689357 | ||||||
chr13:57689430
|
G | T | 1 | a0001c0001t0044g0230 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2797+22597G>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57689430 | ||||||
chr13:57689468
|
T | A | 6 | a0001c0001t0002g0128a0001c0001t0002g0140a0001c0001t0037g0012others(3): Show | 6 | HG02257.hp1 HG02258.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.2797+22635T>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57689468 | ||||||
chr13:57689673
|
A | G | 1 | a0001c0001t0002g0093 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2797+22840A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57689673 | ||||||
chr13:57689868
|
A | T | 2 | a0001c0001t0007g0180a0001c0001t0007g0181 | 2 | NA18998.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.2797+23035A>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57689868 | ||||||
chr13:57689881
|
T | C | 2 | a0001c0001t0018g0060a0001c0001t0018g0203 | 2 | HG02055.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.2797+23048T>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57689881 | ||||||
chr13:57689926
|
T | C | 20 | a0001c0001t0002g0266a0001c0001t0006g0016a0001c0001t0006g0058others(17): Show | 20 | HG00140.hp2 HG01069.hp2 HG01106.hp2 others(17): Show |
intron_variant | MODIFIER | c.2797+23093T>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57689926 | ||||||
chr13:57689994
|
G | A | 2 | a0001c0001t0018g0060a0001c0001t0018g0203 | 2 | HG02055.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.2797+23161G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57689994 | ||||||
chr13:57690087
|
A | C | 56 | a0001c0001t0002g0068a0001c0001t0002g0089a0001c0001t0002g0091others(53): Show | 56 | HG00544.hp1 HG00544.hp2 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.2797+23254A>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57690087 | ||||||
chr13:57690116
|
A | ATT | 20 | a0001c0001t0002g0266a0001c0001t0006g0016a0001c0001t0006g0058others(17): Show | 20 | HG00140.hp2 HG01069.hp2 HG01106.hp2 others(17): Show |
intron_variant | MODIFIER | c.2797+23284_2797+23 others(8): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr13 | 57690116 | |||||
chr13:57690118
|
A | C | 20 | a0001c0001t0002g0266a0001c0001t0006g0016a0001c0001t0006g0058others(17): Show | 20 | HG00140.hp2 HG01069.hp2 HG01106.hp2 others(17): Show |
intron_variant | MODIFIER | c.2797+23285A>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57690118 | ||||||
chr13:57690329
|
T | C | 128 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(125): Show | 129 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(126): Show |
intron_variant | MODIFIER | c.2797+23496T>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57690329 | ||||||
chr13:57690373
|
A | G | 1 | a0001c0001t0006g0242 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.2797+23540A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57690373 | ||||||
chr13:57690451
|
T | G | 2 | a0001c0001t0002g0080a0001c0001t0002g0120 | 2 | NA18943.hp1 NA18948.hp1 |
intron_variant | MODIFIER | c.2797+23618T>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57690451 | ||||||
chr13:57690475
|
G | C | 2 | a0001c0001t0005g0131a0001c0001t0005g0133 | 2 | HG02615.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.2797+23642G>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57690475 | ||||||
chr13:57690545
|
T | C | 263 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(260): Show | 267 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.2797+23712T>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57690545 | ||||||
chr13:57690591
|
C | A | 20 | a0001c0001t0002g0266a0001c0001t0006g0016a0001c0001t0006g0058others(17): Show | 20 | HG00140.hp2 HG01069.hp2 HG01106.hp2 others(17): Show |
intron_variant | MODIFIER | c.2797+23758C>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57690591 | ||||||
chr13:57690618
|
C | T | 2 | a0001c0001t0018g0060a0001c0001t0018g0203 | 2 | HG02055.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.2797+23785C>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57690618 | ||||||
chr13:57690845
|
G | A | 19 | a0001c0001t0006g0016a0001c0001t0006g0058a0001c0001t0006g0083others(16): Show | 19 | HG00140.hp2 HG01069.hp2 HG01106.hp2 others(16): Show |
intron_variant | MODIFIER | c.2797+24012G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57690845 | ||||||
chr13:57690927
|
T | G | 19 | a0001c0001t0006g0016a0001c0001t0006g0058a0001c0001t0006g0083others(16): Show | 19 | HG00140.hp2 HG01069.hp2 HG01106.hp2 others(16): Show |
intron_variant | MODIFIER | c.2797+24094T>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57690927 | ||||||
chr13:57690950
|
T | A | 19 | a0001c0001t0006g0016a0001c0001t0006g0058a0001c0001t0006g0083others(16): Show | 19 | HG00140.hp2 HG01069.hp2 HG01106.hp2 others(16): Show |
intron_variant | MODIFIER | c.2797+24117T>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57690950 | ||||||
chr13:57690972
|
T | C | 1 | a0001c0001t0002g0205 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.2797+24139T>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57690972 | ||||||
chr13:57691272
|
A | G | 1 | a0001c0001t0016g0286 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.2797+24439A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57691272 | ||||||
chr13:57691301
|
T | G | 1 | a0001c0001t0025g0204 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.2797+24468T>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57691301 | ||||||
chr13:57691462
|
G | A | 263 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(260): Show | 267 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.2797+24629G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57691462 | ||||||
chr13:57691786
|
T | C | 19 | a0001c0001t0006g0016a0001c0001t0006g0058a0001c0001t0006g0083others(16): Show | 19 | HG00140.hp2 HG01069.hp2 HG01106.hp2 others(16): Show |
intron_variant | MODIFIER | c.2797+24953T>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57691786 | ||||||
chr13:57691843
|
T | C | 2 | a0001c0001t0018g0060a0001c0001t0018g0203 | 2 | HG02055.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.2797+25010T>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57691843 | ||||||
chr13:57692042
|
T | G | 1 | a0001c0001t0008g0035 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2797+25209T>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57692042 | ||||||
chr13:57692088
|
C | T | 244 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(241): Show | 248 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(245): Show |
intron_variant | MODIFIER | c.2797+25255C>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57692088 | ||||||
chr13:57692188
|
G | A | 7 | a0001c0001t0002g0128a0001c0001t0002g0140a0001c0001t0034g0247others(4): Show | 7 | HG02257.hp1 HG02257.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.2797+25355G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57692188 | ||||||
chr13:57692347
|
T | A | 9 | a0001c0001t0001g0161a0001c0001t0002g0266a0001c0001t0003g0011others(6): Show | 9 | HG00323.hp1 HG00558.hp1 HG00735.hp1 others(6): Show |
intron_variant | MODIFIER | c.2797+25514T>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57692347 | ||||||
chr13:57692406
|
C | G | 1 | a0001c0001t0004g0303 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2797+25573C>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57692406 | ||||||
chr13:57692480
|
C | G | 36 | a0001c0001t0002g0068a0001c0001t0002g0106a0001c0001t0002g0112others(33): Show | 36 | HG00544.hp1 HG00544.hp2 HG00597.hp1 others(33): Show |
intron_variant | MODIFIER | c.2797+25647C>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57692480 | ||||||
chr13:57692527
|
A | G | 16 | a0001c0001t0002g0089a0001c0001t0002g0091a0001c0001t0002g0098others(13): Show | 16 | HG01891.hp1 HG02280.hp1 HG02615.hp1 others(13): Show |
intron_variant | MODIFIER | c.2797+25694A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57692527 | ||||||
chr13:57692554
|
G | T | 19 | a0001c0001t0006g0016a0001c0001t0006g0058a0001c0001t0006g0083others(16): Show | 19 | HG00140.hp2 HG01069.hp2 HG01106.hp2 others(16): Show |
intron_variant | MODIFIER | c.2797+25721G>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57692554 | ||||||
chr13:57692700
|
A | T | 2 | a0001c0001t0007g0078a0001c0001t0007g0187 | 2 | HG00558.hp1 HG02080.hp2 |
intron_variant | MODIFIER | c.2797+25867A>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57692700 | ||||||
chr13:57692738
|
T | G | 1 | a0001c0001t0043g0087 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2797+25905T>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57692738 | ||||||
chr13:57692809
|
G | A | 20 | a0001c0001t0002g0266a0001c0001t0006g0016a0001c0001t0006g0058others(17): Show | 20 | HG00140.hp2 HG01069.hp2 HG01106.hp2 others(17): Show |
intron_variant | MODIFIER | c.2797+25976G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57692809 | ||||||
chr13:57692937
|
A | G | 1 | a0001c0001t0044g0230 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2797+26104A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57692937 | ||||||
chr13:57693023
|
C | A | 20 | a0001c0001t0002g0266a0001c0001t0006g0016a0001c0001t0006g0058others(17): Show | 20 | HG00140.hp2 HG01069.hp2 HG01106.hp2 others(17): Show |
intron_variant | MODIFIER | c.2797+26190C>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57693023 | ||||||
chr13:57693141
|
A | T | 58 | a0001c0001t0001g0002a0001c0001t0002g0068a0001c0001t0002g0089others(55): Show | 58 | HG00544.hp1 HG00544.hp2 HG00597.hp1 others(55): Show |
intron_variant | MODIFIER | c.2797+26308A>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57693141 | ||||||
chr13:57693143
|
G | A | 19 | a0001c0001t0006g0016a0001c0001t0006g0058a0001c0001t0006g0083others(16): Show | 19 | HG00140.hp2 HG01069.hp2 HG01106.hp2 others(16): Show |
intron_variant | MODIFIER | c.2797+26310G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57693143 | ||||||
chr13:57693186
|
A | G | 5 | a0001c0001t0003g0064a0001c0001t0003g0070a0001c0001t0003g0071others(2): Show | 5 | HG01256.hp2 HG01943.hp1 HG01952.hp1 others(2): Show |
intron_variant | MODIFIER | c.2797+26353A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57693186 | ||||||
chr13:57693214
|
CT | C | 302 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0010others(299): Show | 306 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(303): Show |
intron_variant | MODIFIER | c.2797+26391delT | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr13 | 57693214 | |||||
chr13:57693229
|
T | C | 3 | a0001c0001t0004g0092a0001c0001t0005g0147a0001c0001t0042g0279 | 3 | HG01891.hp2 HG02451.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.2797+26396T>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57693229 | ||||||
chr13:57693277
|
A | G | 2 | a0001c0001t0018g0060a0001c0001t0018g0203 | 2 | HG02055.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.2797+26444A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57693277 | ||||||
chr13:57693278
|
A | T | 2 | a0001c0001t0004g0199a0001c0001t0012g0031 | 2 | NA19011.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.2797+26445A>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57693278 | ||||||
chr13:57693279
|
T | A | 19 | a0001c0001t0006g0016a0001c0001t0006g0058a0001c0001t0006g0083others(16): Show | 19 | HG00140.hp2 HG01069.hp2 HG01106.hp2 others(16): Show |
intron_variant | MODIFIER | c.2797+26446T>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57693279 | ||||||
chr13:57693295
|
T | C | 4 | a0001c0001t0001g0059a0001c0001t0001g0129a0001c0001t0010g0237others(1): Show | 4 | HG01943.hp2 HG02258.hp2 NA18992.hp2 others(1): Show |
intron_variant | MODIFIER | c.2797+26462T>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57693295 | ||||||
chr13:57693307
|
C | T | 4 | a0001c0001t0001g0059a0001c0001t0001g0129a0001c0001t0010g0237others(1): Show | 4 | HG01943.hp2 HG02258.hp2 NA18992.hp2 others(1): Show |
intron_variant | MODIFIER | c.2797+26474C>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57693307 | ||||||
chr13:57693315
|
C | CAT | 13 | a0001c0001t0001g0150a0001c0001t0001g0161a0001c0001t0001g0218others(10): Show | 13 | HG00639.hp1 HG00735.hp1 HG01123.hp2 others(10): Show |
intron_variant | MODIFIER | c.2797+26511_2797+26 others(8): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr13 | 57693315 | |||||
chr13:57693315
|
C | CATAT | 6 | a0001c0001t0001g0159a0001c0001t0002g0266a0001c0001t0011g0047others(3): Show | 6 | HG00280.hp1 HG01243.hp2 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.2797+26509_2797+26 others(10): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr13 | 57693315 | |||||
chr13:57693315
|
C | CATATAT | 8 | a0001c0001t0001g0065a0001c0001t0001g0191a0001c0001t0002g0135others(5): Show | 8 | HG00639.hp2 HG01255.hp2 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.2797+26507_2797+26 others(12): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr13 | 57693315 | |||||
chr13:57693315
|
C | CATATATA others(1): Show |
19 | a0001c0001t0001g0002a0001c0001t0002g0134a0001c0001t0002g0241others(16): Show | 19 | HG01109.hp2 HG01496.hp1 HG02280.hp2 others(16): Show |
intron_variant | MODIFIER | c.2797+26505_2797+26 others(14): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr13 | 57693315 | |||||
chr13:57693315
|
C | CATATATA others(3): Show |
14 | a0001c0001t0002g0005a0001c0001t0002g0112a0001c0001t0002g0130others(11): Show | 16 | HG00741.hp2 HG01192.hp2 HG01261.hp2 others(13): Show |
intron_variant | MODIFIER | c.2797+26503_2797+26 others(16): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr13 | 57693315 | |||||
chr13:57693315
|
C | CATATATA others(5): Show |
16 | a0001c0001t0002g0089a0001c0001t0002g0102a0001c0001t0002g0120others(13): Show | 16 | HG00673.hp2 HG01993.hp1 HG02074.hp2 others(13): Show |
intron_variant | MODIFIER | c.2797+26501_2797+26 others(18): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr13 | 57693315 | |||||
chr13:57693315
|
C | CATATATA others(7): Show |
19 | a0001c0001t0002g0068a0001c0001t0002g0080a0001c0001t0002g0091others(16): Show | 19 | HG01074.hp1 HG01081.hp2 HG01106.hp1 others(16): Show |
intron_variant | MODIFIER | c.2797+26499_2797+26 others(20): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr13 | 57693315 | |||||
chr13:57693315
|
C | CATATATA others(9): Show |
27 | a0001c0001t0002g0098a0001c0001t0002g0106a0001c0001t0002g0138others(24): Show | 27 | HG01069.hp1 HG01257.hp1 HG01258.hp1 others(24): Show |
intron_variant | MODIFIER | c.2797+26497_2797+26 others(22): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr13 | 57693315 | |||||
chr13:57693315
|
C | CATATATA others(11): Show |
13 | a0001c0001t0002g0144a0001c0001t0002g0145a0001c0001t0002g0179others(10): Show | 14 | HG00544.hp2 HG00621.hp2 HG00738.hp1 others(11): Show |
intron_variant | MODIFIER | c.2797+26495_2797+26 others(24): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr13 | 57693315 | |||||
chr13:57693315
|
C | CATATATA others(13): Show |
5 | a0001c0001t0002g0198a0001c0001t0002g0256a0001c0001t0002g0277others(2): Show | 5 | HG00544.hp1 HG01099.hp1 NA18962.hp1 others(2): Show |
intron_variant | MODIFIER | c.2797+26493_2797+26 others(26): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr13 | 57693315 | |||||
chr13:57693315
|
C | CATATATA others(15): Show |
4 | a0001c0001t0002g0162a0001c0001t0002g0251a0001c0001t0007g0285others(1): Show | 4 | HG00597.hp1 HG00735.hp2 HG02132.hp1 others(1): Show |
intron_variant | MODIFIER | c.2797+26491_2797+26 others(28): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr13 | 57693315 | |||||
chr13:57693315
|
C | CATATATA others(17): Show |
1 | a0001c0001t0012g0048 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.2797+26489_2797+26 others(30): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr13 | 57693315 | |||||
chr13:57693315
|
CAT | C | 28 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0049others(25): Show | 29 | HG00280.hp2 HG00597.hp2 HG01069.hp2 others(26): Show |
intron_variant | MODIFIER | c.2797+26511_2797+26 others(8): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr13 | 57693315 | |||||
chr13:57693315
|
CATAT | C | 12 | a0001c0001t0006g0016a0001c0001t0006g0105a0001c0001t0006g0125others(9): Show | 12 | HG00140.hp2 HG01106.hp2 HG01175.hp2 others(9): Show |
intron_variant | MODIFIER | c.2797+26509_2797+26 others(10): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr13 | 57693315 | |||||
chr13:57693315
|
CATATAT | C | 7 | a0001c0001t0006g0058a0001c0001t0006g0083a0001c0001t0006g0084others(4): Show | 7 | NA18948.hp2 NA18959.hp2 NA18980.hp2 others(4): Show |
intron_variant | MODIFIER | c.2797+26507_2797+26 others(12): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr13 | 57693315 | |||||
chr13:57693342
|
A | C | 1 | a0001c0001t0006g0125 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.2797+26509A>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57693342 | ||||||
chr13:57693476
|
G | C | 2 | a0001c0004t0005g0061a0001c0004t0005g0062 | 2 | HG02257.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.2797+26643G>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57693476 | ||||||
chr13:57693520
|
G | A | 9 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0086others(6): Show | 9 | HG01109.hp1 HG01884.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.2797+26687G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57693520 | ||||||
chr13:57693522
|
G | A | 19 | a0001c0001t0006g0016a0001c0001t0006g0058a0001c0001t0006g0083others(16): Show | 19 | HG00140.hp2 HG01069.hp2 HG01106.hp2 others(16): Show |
intron_variant | MODIFIER | c.2797+26689G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57693522 | ||||||
chr13:57693704
|
A | G | 6 | a0001c0001t0002g0128a0001c0001t0002g0140a0001c0001t0037g0012others(3): Show | 6 | HG02257.hp1 HG02258.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.2797+26871A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57693704 | ||||||
chr13:57693871
|
G | A | 1 | a0001c0001t0001g0010 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.2797+27038G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57693871 | ||||||
chr13:57693935
|
G | GTAGGTAC others(7): Show |
1 | a0001c0001t0006g0125 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.2797+27103_2797+27 others(20): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr13 | 57693935 | |||||
chr13:57693966
|
G | GT | 7 | a0001c0001t0003g0280a0001c0001t0003g0284a0001c0001t0003g0299others(4): Show | 7 | HG02027.hp1 HG02132.hp2 NA18967.hp2 others(4): Show |
intron_variant | MODIFIER | c.2797+27145dupT | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr13 | 57693966 | |||||
chr13:57693988
|
G | A | 52 | a0001c0001t0002g0005a0001c0001t0002g0080a0001c0001t0002g0120others(49): Show | 55 | HG00673.hp2 HG00741.hp2 HG01081.hp2 others(52): Show |
intron_variant | MODIFIER | c.2797+27155G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57693988 | ||||||
chr13:57694228
|
A | G | 1 | a0001c0001t0056g0056 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.2797+27395A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57694228 | ||||||
chr13:57694240
|
T | G | 1 | a0001c0001t0005g0278 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2797+27407T>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57694240 | ||||||
chr13:57694487
|
A | G | 1 | a0001c0001t0009g0221 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.2797+27654A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57694487 | ||||||
chr13:57694784
|
A | T | 116 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(113): Show | 117 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.2797+27951A>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57694784 | ||||||
chr13:57694818
|
G | A | 1 | a0001c0001t0007g0121 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.2797+27985G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57694818 | ||||||
chr13:57694912
|
T | C | 1 | a0001c0001t0001g0218 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.2797+28079T>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57694912 | ||||||
chr13:57694919
|
G | C | 1 | a0001c0001t0004g0243 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.2797+28086G>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57694919 | ||||||
chr13:57695040
|
A | C | 1 | a0001c0001t0021g0074 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.2797+28207A>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57695040 | ||||||
chr13:57695332
|
T | A | 1 | a0001c0001t0003g0246 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.2797+28499T>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57695332 | ||||||
chr13:57695340
|
A | G | 8 | a0001c0001t0001g0161a0001c0001t0003g0011a0001c0001t0007g0078others(5): Show | 8 | HG00323.hp1 HG00558.hp1 HG00735.hp1 others(5): Show |
intron_variant | MODIFIER | c.2797+28507A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57695340 | ||||||
chr13:57695366
|
T | C | 5 | a0001c0001t0002g0128a0001c0001t0002g0140a0001c0001t0037g0012others(2): Show | 5 | HG02257.hp1 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.2797+28533T>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57695366 | ||||||
chr13:57695421
|
GAGAA | G | 263 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(260): Show | 267 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.2797+28614_2797+28 others(10): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr13 | 57695421 | |||||
chr13:57695540
|
T | C | 1 | a0001c0001t0011g0057 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.2797+28707T>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57695540 | ||||||
chr13:57695629
|
C | T | 112 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(109): Show | 113 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(110): Show |
intron_variant | MODIFIER | c.2797+28796C>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57695629 | ||||||
chr13:57695636
|
C | T | 1 | a0001c0001t0003g0072 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.2797+28803C>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57695636 | ||||||
chr13:57695667
|
G | T | 1 | a0001c0001t0001g0189 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.2797+28834G>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57695667 | ||||||
chr13:57695997
|
A | G | 1 | a0001c0001t0003g0073 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.2798-28615A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57695997 | ||||||
chr13:57696049
|
G | A | 7 | a0001c0001t0004g0303a0001c0001t0005g0122a0001c0001t0005g0123others(4): Show | 7 | HG02280.hp2 HG02615.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.2798-28563G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57696049 | ||||||
chr13:57696090
|
T | C | 89 | a0001c0001t0002g0005a0001c0001t0002g0068a0001c0001t0002g0080others(86): Show | 92 | HG00544.hp1 HG00544.hp2 HG00597.hp1 others(89): Show |
intron_variant | MODIFIER | c.2798-28522T>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57696090 | ||||||
chr13:57696103
|
A | C | 2 | a0001c0001t0006g0083a0001c0001t0006g0084 | 2 | NA19010.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.2798-28509A>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57696103 | ||||||
chr13:57696113
|
G | A | 1 | a0001c0001t0002g0251 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.2798-28499G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57696113 | ||||||
chr13:57696138
|
A | G | 1 | a0001c0001t0046g0095 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2798-28474A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57696138 | ||||||
chr13:57696452
|
A | G | 2 | a0001c0001t0002g0240a0001c0001t0005g0291 | 2 | NA18988.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.2798-28160A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57696452 | ||||||
chr13:57696524
|
C | T | 25 | a0001c0001t0002g0266a0001c0001t0006g0016a0001c0001t0006g0058others(22): Show | 25 | HG00140.hp2 HG01069.hp2 HG01106.hp2 others(22): Show |
intron_variant | MODIFIER | c.2798-28088C>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57696524 | ||||||
chr13:57696526
|
C | CA | 25 | a0001c0001t0002g0266a0001c0001t0006g0016a0001c0001t0006g0058others(22): Show | 25 | HG00140.hp2 HG01069.hp2 HG01106.hp2 others(22): Show |
intron_variant | MODIFIER | c.2798-28078dupA | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr13 | 57696526 | |||||
chr13:57696583
|
G | A | 25 | a0001c0001t0002g0266a0001c0001t0006g0016a0001c0001t0006g0058others(22): Show | 25 | HG00140.hp2 HG01069.hp2 HG01106.hp2 others(22): Show |
intron_variant | MODIFIER | c.2798-28029G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57696583 | ||||||
chr13:57696587
|
C | G | 1 | a0001c0001t0043g0087 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2798-28025C>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57696587 | ||||||
chr13:57696594
|
T | C | 1 | a0001c0001t0009g0029 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.2798-28018T>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57696594 | ||||||
chr13:57696602
|
A | G | 16 | a0001c0001t0002g0068a0001c0001t0002g0216a0001c0001t0002g0235others(13): Show | 16 | HG00735.hp2 HG00738.hp1 HG01069.hp1 others(13): Show |
intron_variant | MODIFIER | c.2798-28010A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57696602 | ||||||
chr13:57696633
|
A | G | 1 | a0001c0001t0044g0230 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2798-27979A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57696633 | ||||||
chr13:57696681
|
A | G | 2 | a0001c0001t0002g0005a0001c0001t0003g0226 | 3 | HG00741.hp2 HG01192.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.2798-27931A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57696681 | ||||||
chr13:57696722
|
C | T | 7 | a0001c0001t0004g0303a0001c0001t0005g0122a0001c0001t0005g0123others(4): Show | 7 | HG02280.hp2 HG02615.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.2798-27890C>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57696722 | ||||||
chr13:57696870
|
A | G | 25 | a0001c0001t0002g0266a0001c0001t0006g0016a0001c0001t0006g0058others(22): Show | 25 | HG00140.hp2 HG01069.hp2 HG01106.hp2 others(22): Show |
intron_variant | MODIFIER | c.2798-27742A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57696870 | ||||||
chr13:57697048
|
A | G | 2 | a0001c0001t0024g0222a0001c0001t0026g0248 | 2 | NA19004.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.2798-27564A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57697048 | ||||||
chr13:57697192
|
G | C | 7 | a0001c0001t0004g0303a0001c0001t0005g0122a0001c0001t0005g0123others(4): Show | 7 | HG02280.hp2 HG02615.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.2798-27420G>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57697192 | ||||||
chr13:57697218
|
A | T | 264 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(261): Show | 268 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(265): Show |
intron_variant | MODIFIER | c.2798-27394A>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57697218 | ||||||
chr13:57697245
|
T | G | 1 | a0001c0001t0002g0145 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2798-27367T>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57697245 | ||||||
chr13:57697327
|
A | G | 1 | a0001c0001t0003g0246 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.2798-27285A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57697327 | ||||||
chr13:57697485
|
T | G | 2 | a0001c0001t0018g0060a0001c0001t0018g0203 | 2 | HG02055.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.2798-27127T>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57697485 | ||||||
chr13:57697495
|
A | G | 10 | a0001c0001t0006g0016a0001c0001t0006g0105a0001c0001t0006g0168others(7): Show | 10 | HG00140.hp2 HG01069.hp2 HG01978.hp2 others(7): Show |
intron_variant | MODIFIER | c.2798-27117A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57697495 | ||||||
chr13:57697591
|
T | TCTC | 25 | a0001c0001t0002g0266a0001c0001t0006g0016a0001c0001t0006g0058others(22): Show | 25 | HG00140.hp2 HG01069.hp2 HG01106.hp2 others(22): Show |
intron_variant | MODIFIER | c.2798-27019_2798-27 others(9): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr13 | 57697591 | |||||
chr13:57697594
|
G | T | 2 | a0001c0001t0018g0060a0001c0001t0018g0203 | 2 | HG02055.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.2798-27018G>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57697594 | ||||||
chr13:57697726
|
A | C | 25 | a0001c0001t0002g0266a0001c0001t0006g0016a0001c0001t0006g0058others(22): Show | 25 | HG00140.hp2 HG01069.hp2 HG01106.hp2 others(22): Show |
intron_variant | MODIFIER | c.2798-26886A>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57697726 | ||||||
chr13:57697774
|
AT | A | 6 | a0001c0001t0002g0128a0001c0001t0002g0140a0001c0001t0037g0012others(3): Show | 6 | HG02257.hp1 HG02258.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.2798-26826delT | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr13 | 57697774 | |||||
chr13:57697850
|
G | A | 25 | a0001c0001t0002g0266a0001c0001t0006g0016a0001c0001t0006g0058others(22): Show | 25 | HG00140.hp2 HG01069.hp2 HG01106.hp2 others(22): Show |
intron_variant | MODIFIER | c.2798-26762G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57697850 | ||||||
chr13:57697862
|
C | T | 1 | a0007c0008t0045g0269 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.2798-26750C>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57697862 | ||||||
chr13:57697936
|
C | A | 126 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(123): Show | 127 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(124): Show |
intron_variant | MODIFIER | c.2798-26676C>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57697936 | ||||||
chr13:57697980
|
C | T | 25 | a0001c0001t0002g0266a0001c0001t0006g0016a0001c0001t0006g0058others(22): Show | 25 | HG00140.hp2 HG01069.hp2 HG01106.hp2 others(22): Show |
intron_variant | MODIFIER | c.2798-26632C>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57697980 | ||||||
chr13:57698035
|
A | G | 25 | a0001c0001t0002g0266a0001c0001t0006g0016a0001c0001t0006g0058others(22): Show | 25 | HG00140.hp2 HG01069.hp2 HG01106.hp2 others(22): Show |
intron_variant | MODIFIER | c.2798-26577A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57698035 | ||||||
chr13:57698287
|
A | T | 261 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(258): Show | 265 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(262): Show |
intron_variant | MODIFIER | c.2798-26325A>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57698287 | ||||||
chr13:57698686
|
AC | A | 149 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(146): Show | 150 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(147): Show |
intron_variant | MODIFIER | c.2798-25925delC | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57698686 | ||||||
chr13:57698708
|
G | A | 1 | a0001c0001t0001g0150 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.2798-25904G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57698708 | ||||||
chr13:57698927
|
A | G | 25 | a0001c0001t0002g0266a0001c0001t0006g0016a0001c0001t0006g0058others(22): Show | 25 | HG00140.hp2 HG01069.hp2 HG01106.hp2 others(22): Show |
intron_variant | MODIFIER | c.2798-25685A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57698927 | ||||||
chr13:57698970
|
G | C | 25 | a0001c0001t0002g0266a0001c0001t0006g0016a0001c0001t0006g0058others(22): Show | 25 | HG00140.hp2 HG01069.hp2 HG01106.hp2 others(22): Show |
intron_variant | MODIFIER | c.2798-25642G>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57698970 | ||||||
chr13:57698971
|
C | A | 1 | a0001c0001t0046g0095 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2798-25641C>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57698971 | ||||||
chr13:57699075
|
C | CTTTT | 25 | a0001c0001t0002g0266a0001c0001t0006g0016a0001c0001t0006g0058others(22): Show | 25 | HG00140.hp2 HG01069.hp2 HG01106.hp2 others(22): Show |
intron_variant | MODIFIER | c.2798-25537_2798-25 others(10): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57699075 | ||||||
chr13:57699076
|
A | G | 25 | a0001c0001t0002g0266a0001c0001t0006g0016a0001c0001t0006g0058others(22): Show | 25 | HG00140.hp2 HG01069.hp2 HG01106.hp2 others(22): Show |
intron_variant | MODIFIER | c.2798-25536A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57699076 | ||||||
chr13:57699078
|
T | C | 25 | a0001c0001t0002g0266a0001c0001t0006g0016a0001c0001t0006g0058others(22): Show | 25 | HG00140.hp2 HG01069.hp2 HG01106.hp2 others(22): Show |
intron_variant | MODIFIER | c.2798-25534T>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57699078 | ||||||
chr13:57699087
|
T | C | 1 | a0001c0001t0011g0021 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.2798-25525T>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57699087 | ||||||
chr13:57699152
|
T | G | 25 | a0001c0001t0002g0266a0001c0001t0006g0016a0001c0001t0006g0058others(22): Show | 25 | HG00140.hp2 HG01069.hp2 HG01106.hp2 others(22): Show |
intron_variant | MODIFIER | c.2798-25460T>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57699152 | ||||||
chr13:57699249
|
A | G | 1 | a0001c0001t0002g0009 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2798-25363A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57699249 | ||||||
chr13:57699270
|
G | A | 25 | a0001c0001t0002g0266a0001c0001t0006g0016a0001c0001t0006g0058others(22): Show | 25 | HG00140.hp2 HG01069.hp2 HG01106.hp2 others(22): Show |
intron_variant | MODIFIER | c.2798-25342G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57699270 | ||||||
chr13:57699413
|
G | A | 1 | a0001c0001t0044g0230 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2798-25199G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57699413 | ||||||
chr13:57699434
|
A | G | 1 | a0001c0001t0003g0268 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.2798-25178A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57699434 | ||||||
chr13:57699603
|
G | A | 25 | a0001c0001t0002g0266a0001c0001t0006g0016a0001c0001t0006g0058others(22): Show | 25 | HG00140.hp2 HG01069.hp2 HG01106.hp2 others(22): Show |
intron_variant | MODIFIER | c.2798-25009G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57699603 | ||||||
chr13:57699666
|
T | A | 26 | a0001c0001t0002g0266a0001c0001t0006g0016a0001c0001t0006g0058others(23): Show | 26 | HG00140.hp2 HG01069.hp2 HG01106.hp2 others(23): Show |
intron_variant | MODIFIER | c.2798-24946T>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57699666 | ||||||
chr13:57699699
|
T | C | 2 | a0001c0001t0003g0253a0001c0001t0008g0053 | 2 | HG00621.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.2798-24913T>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57699699 | ||||||
chr13:57699743
|
C | G | 6 | a0001c0001t0002g0128a0001c0001t0002g0140a0001c0001t0037g0012others(3): Show | 6 | HG02257.hp1 HG02258.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.2798-24869C>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57699743 | ||||||
chr13:57699751
|
G | A | 25 | a0001c0001t0002g0266a0001c0001t0006g0016a0001c0001t0006g0058others(22): Show | 25 | HG00140.hp2 HG01069.hp2 HG01106.hp2 others(22): Show |
intron_variant | MODIFIER | c.2798-24861G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57699751 | ||||||
chr13:57699765
|
A | G | 25 | a0001c0001t0002g0266a0001c0001t0006g0016a0001c0001t0006g0058others(22): Show | 25 | HG00140.hp2 HG01069.hp2 HG01106.hp2 others(22): Show |
intron_variant | MODIFIER | c.2798-24847A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57699765 | ||||||
chr13:57699779
|
T | C | 25 | a0001c0001t0002g0266a0001c0001t0006g0016a0001c0001t0006g0058others(22): Show | 25 | HG00140.hp2 HG01069.hp2 HG01106.hp2 others(22): Show |
intron_variant | MODIFIER | c.2798-24833T>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57699779 | ||||||
chr13:57699814
|
A | T | 4 | a0001c0001t0006g0105a0001c0001t0006g0168a0001c0001t0006g0212others(1): Show | 4 | HG01978.hp2 HG01981.hp2 NA20905.hp1 others(1): Show |
intron_variant | MODIFIER | c.2798-24798A>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57699814 | ||||||
chr13:57700038
|
T | C | 25 | a0001c0001t0002g0266a0001c0001t0006g0016a0001c0001t0006g0058others(22): Show | 25 | HG00140.hp2 HG01069.hp2 HG01106.hp2 others(22): Show |
intron_variant | MODIFIER | c.2798-24574T>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57700038 | ||||||
chr13:57700145
|
A | G | 25 | a0001c0001t0002g0266a0001c0001t0006g0016a0001c0001t0006g0058others(22): Show | 25 | HG00140.hp2 HG01069.hp2 HG01106.hp2 others(22): Show |
intron_variant | MODIFIER | c.2798-24467A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57700145 | ||||||
chr13:57700313
|
C | A | 1 | a0001c0001t0003g0268 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.2798-24299C>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57700313 | ||||||
chr13:57700321
|
C | CT | 13 | a0001c0001t0001g0159a0001c0001t0003g0041a0001c0001t0003g0151others(10): Show | 13 | HG00323.hp2 HG01433.hp2 HG01515.hp2 others(10): Show |
intron_variant | MODIFIER | c.2798-24275dupT | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr13 | 57700321 | |||||
chr13:57700321
|
CT | C | 29 | a0001c0001t0001g0076a0001c0001t0001g0259a0001c0001t0002g0089others(26): Show | 29 | HG01496.hp1 HG01891.hp1 HG01943.hp1 others(26): Show |
intron_variant | MODIFIER | c.2798-24275delT | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr13 | 57700321 | |||||
chr13:57700379
|
C | T | 151 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(148): Show | 152 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(149): Show |
intron_variant | MODIFIER | c.2798-24233C>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57700379 | ||||||
chr13:57700380
|
G | A | 6 | a0001c0001t0004g0085a0001c0001t0012g0043a0001c0001t0012g0044others(3): Show | 6 | NA18942.hp2 NA18962.hp1 NA18993.hp1 others(3): Show |
intron_variant | MODIFIER | c.2798-24232G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57700380 | ||||||
chr13:57700402
|
A | T | 261 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(258): Show | 265 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(262): Show |
intron_variant | MODIFIER | c.2798-24210A>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57700402 | ||||||
chr13:57700464
|
G | A | 1 | a0001c0006t0003g0114 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.2798-24148G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57700464 | ||||||
chr13:57700466
|
G | T | 2 | a0001c0001t0018g0060a0001c0001t0018g0203 | 2 | HG02055.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.2798-24146G>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57700466 | ||||||
chr13:57700659
|
T | C | 261 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(258): Show | 265 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(262): Show |
intron_variant | MODIFIER | c.2798-23953T>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57700659 | ||||||
chr13:57700806
|
A | G | 1 | a0001c0003t0002g0287 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.2798-23806A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57700806 | ||||||
chr13:57700909
|
C | A | 261 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(258): Show | 265 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(262): Show |
intron_variant | MODIFIER | c.2798-23703C>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57700909 | ||||||
chr13:57700915
|
A | G | 1 | a0001c0012t0001g0094 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2798-23697A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57700915 | ||||||
chr13:57701004
|
A | G | 89 | a0001c0001t0002g0005a0001c0001t0002g0068a0001c0001t0002g0080others(86): Show | 92 | HG00544.hp1 HG00544.hp2 HG00597.hp1 others(89): Show |
intron_variant | MODIFIER | c.2798-23608A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57701004 | ||||||
chr13:57701033
|
A | G | 5 | a0001c0001t0005g0132a0001c0001t0005g0275a0001c0001t0005g0276others(2): Show | 5 | HG01496.hp1 HG02451.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.2798-23579A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57701033 | ||||||
chr13:57701040
|
T | C | 1 | a0001c0001t0001g0150 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.2798-23572T>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57701040 | ||||||
chr13:57701267
|
C | CGTTT | 5 | a0001c0001t0002g0128a0001c0001t0002g0140a0001c0001t0037g0012others(2): Show | 5 | HG02257.hp1 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.2798-23324_2798-23 others(10): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr13 | 57701267 | |||||
chr13:57701539
|
T | TG | 302 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(299): Show | 307 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(304): Show |
intron_variant | MODIFIER | c.2798-23073_2798-23 others(7): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57701539 | ||||||
chr13:57701652
|
G | A | 3 | a0001c0001t0001g0139a0001c0001t0010g0090a0001c0001t0010g0274 | 3 | HG01255.hp1 HG03041.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.2798-22960G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57701652 | ||||||
chr13:57701793
|
G | T | 1 | a0001c0001t0003g0273 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.2798-22819G>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57701793 | ||||||
chr13:57701872
|
T | C | 2 | a0001c0001t0002g0086a0001c0001t0002g0097 | 2 | HG01109.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.2798-22740T>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57701872 | ||||||
chr13:57701925
|
G | A | 1 | a0001c0001t0002g0142 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2798-22687G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57701925 | ||||||
chr13:57702231
|
G | A | 261 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(258): Show | 265 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(262): Show |
intron_variant | MODIFIER | c.2798-22381G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57702231 | ||||||
chr13:57702295
|
T | C | 15 | a0001c0001t0001g0002a0001c0001t0001g0127a0001c0001t0002g0205others(12): Show | 15 | HG00597.hp2 HG02027.hp2 HG02615.hp1 others(12): Show |
intron_variant | MODIFIER | c.2798-22317T>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57702295 | ||||||
chr13:57702447
|
G | A | 3 | a0001c0001t0002g0008a0001c0001t0002g0093a0001c0001t0002g0234 | 3 | HG01884.hp1 HG02622.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.2798-22165G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57702447 | ||||||
chr13:57703044
|
T | A | 24 | a0001c0001t0006g0016a0001c0001t0006g0058a0001c0001t0006g0083others(21): Show | 24 | HG00140.hp2 HG01069.hp2 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.2798-21568T>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57703044 | ||||||
chr13:57703172
|
C | A | 261 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(258): Show | 265 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(262): Show |
intron_variant | MODIFIER | c.2798-21440C>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57703172 | ||||||
chr13:57703279
|
A | T | 3 | a0001c0001t0002g0008a0001c0001t0002g0093a0001c0001t0002g0234 | 3 | HG01884.hp1 HG02622.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.2798-21333A>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57703279 | ||||||
chr13:57703405
|
G | A | 1 | a0001c0001t0007g0194 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.2798-21207G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57703405 | ||||||
chr13:57703708
|
C | T | 4 | a0001c0001t0005g0124a0001c0001t0005g0126a0001c0001t0005g0131others(1): Show | 4 | HG02615.hp2 HG03225.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.2798-20904C>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57703708 | ||||||
chr13:57703741
|
T | A | 6 | a0001c0001t0002g0009a0001c0001t0002g0086a0001c0001t0002g0097others(3): Show | 6 | HG01109.hp1 HG02572.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.2798-20871T>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57703741 | ||||||
chr13:57703791
|
A | C | 1 | a0001c0001t0003g0151 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.2798-20821A>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57703791 | ||||||
chr13:57704087
|
G | A | 261 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(258): Show | 265 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(262): Show |
intron_variant | MODIFIER | c.2798-20525G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57704087 | ||||||
chr13:57704146
|
T | C | 1 | a0001c0001t0015g0014 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2798-20466T>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57704146 | ||||||
chr13:57704277
|
A | T | 1 | a0001c0001t0002g0009 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2798-20335A>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57704277 | ||||||
chr13:57704337
|
C | G | 1 | a0001c0001t0024g0222 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.2798-20275C>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57704337 | ||||||
chr13:57704386
|
G | T | 1 | a0001c0001t0007g0121 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.2798-20226G>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57704386 | ||||||
chr13:57704393
|
A | G | 294 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(291): Show | 299 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(296): Show |
intron_variant | MODIFIER | c.2798-20219A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57704393 | ||||||
chr13:57704440
|
T | A | 1 | a0001c0001t0004g0117 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.2798-20172T>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57704440 | ||||||
chr13:57704853
|
A | T | 1 | a0001c0001t0011g0021 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.2798-19759A>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57704853 | ||||||
chr13:57704896
|
A | G | 1 | a0001c0001t0002g0093 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2798-19716A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57704896 | ||||||
chr13:57705051
|
C | T | 1 | a0001c0001t0001g0006 | 2 | NA18969.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.2798-19561C>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57705051 | ||||||
chr13:57705260
|
G | C | 261 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(258): Show | 265 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(262): Show |
intron_variant | MODIFIER | c.2798-19352G>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57705260 | ||||||
chr13:57705654
|
A | G | 69 | a0001c0001t0002g0005a0001c0001t0002g0068a0001c0001t0002g0080others(66): Show | 70 | HG00544.hp1 HG00544.hp2 HG00597.hp1 others(67): Show |
intron_variant | MODIFIER | c.2798-18958A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57705654 | ||||||
chr13:57705933
|
T | G | 1 | a0001c0001t0002g0301 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2798-18679T>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57705933 | ||||||
chr13:57706010
|
A | C | 261 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(258): Show | 265 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(262): Show |
intron_variant | MODIFIER | c.2798-18602A>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57706010 | ||||||
chr13:57706015
|
TA | T | 12 | a0001c0001t0001g0129a0001c0001t0001g0189a0001c0001t0003g0064others(9): Show | 12 | HG01069.hp1 HG01256.hp2 HG01943.hp1 others(9): Show |
intron_variant | MODIFIER | c.2798-18581delA | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr13 | 57706015 | |||||
chr13:57706341
|
C | A | 2 | a0001c0001t0018g0060a0001c0001t0018g0203 | 2 | HG02055.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.2798-18271C>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57706341 | ||||||
chr13:57706447
|
T | C | 7 | a0001c0001t0004g0303a0001c0001t0005g0122a0001c0001t0005g0123others(4): Show | 7 | HG02280.hp2 HG02615.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.2798-18165T>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57706447 | ||||||
chr13:57706618
|
C | A | 1 | a0001c0001t0044g0230 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2798-17994C>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57706618 | ||||||
chr13:57706751
|
C | T | 87 | a0001c0001t0002g0005a0001c0001t0002g0068a0001c0001t0002g0080others(84): Show | 90 | HG00544.hp1 HG00544.hp2 HG00597.hp1 others(87): Show |
intron_variant | MODIFIER | c.2798-17861C>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57706751 | ||||||
chr13:57707334
|
C | CGT | 28 | a0001c0001t0001g0059a0001c0001t0001g0118a0001c0001t0001g0119others(25): Show | 28 | HG00323.hp1 HG00558.hp1 HG00735.hp1 others(25): Show |
intron_variant | MODIFIER | c.2798-17241_2798-17 others(8): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr13 | 57707334 | |||||
chr13:57707334
|
C | CGTGT | 30 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0065others(27): Show | 30 | HG00140.hp1 HG00639.hp2 HG00673.hp1 others(27): Show |
intron_variant | MODIFIER | c.2798-17243_2798-17 others(10): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr13 | 57707334 | |||||
chr13:57707334
|
C | CGTGTGT | 43 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0079others(40): Show | 44 | HG00280.hp1 HG00558.hp2 HG01074.hp2 others(41): Show |
intron_variant | MODIFIER | c.2798-17245_2798-17 others(12): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr13 | 57707334 | |||||
chr13:57707334
|
C | CGTGTGTG others(1): Show |
14 | a0001c0001t0001g0049a0001c0001t0001g0150a0001c0001t0001g0175others(11): Show | 14 | HG00323.hp2 HG00597.hp2 HG01496.hp2 others(11): Show |
intron_variant | MODIFIER | c.2798-17247_2798-17 others(14): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr13 | 57707334 | |||||
chr13:57707334
|
C | CGTGTGTG others(3): Show |
2 | a0001c0001t0001g0139a0001c0001t0010g0090 | 2 | HG01255.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.2798-17249_2798-17 others(16): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr13 | 57707334 | |||||
chr13:57707334
|
C | CGTGTGTG others(5): Show |
1 | a0001c0001t0001g0259 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.2798-17251_2798-17 others(18): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr13 | 57707334 | |||||
chr13:57707334
|
CGT | C | 50 | a0001c0001t0002g0086a0001c0001t0002g0093a0001c0001t0002g0097others(47): Show | 51 | HG00140.hp2 HG00735.hp2 HG01069.hp2 others(48): Show |
intron_variant | MODIFIER | c.2798-17241_2798-17 others(8): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr13 | 57707334 | |||||
chr13:57707334
|
CGTGT | C | 75 | a0001c0001t0002g0005a0001c0001t0002g0009a0001c0001t0002g0068others(72): Show | 77 | HG00544.hp1 HG00544.hp2 HG00597.hp1 others(74): Show |
intron_variant | MODIFIER | c.2798-17243_2798-17 others(10): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr13 | 57707334 | |||||
chr13:57707334
|
CGTGTGT | C | 16 | a0001c0001t0002g0089a0001c0001t0002g0091a0001c0001t0002g0098others(13): Show | 16 | HG01891.hp1 HG02280.hp1 HG02622.hp2 others(13): Show |
intron_variant | MODIFIER | c.2798-17245_2798-17 others(12): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr13 | 57707334 | |||||
chr13:57707334
|
CGTGTGTG others(1): Show |
C | 6 | a0001c0001t0004g0107a0001c0001t0005g0132a0001c0001t0005g0275others(3): Show | 6 | HG01496.hp1 HG02451.hp2 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.2798-17247_2798-17 others(14): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr13 | 57707334 | |||||
chr13:57707334
|
CGTGTGTG others(3): Show |
C | 1 | a0001c0001t0015g0013 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2798-17249_2798-17 others(16): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr13 | 57707334 | |||||
chr13:57707560
|
A | G | 3 | a0001c0001t0014g0004a0001c0001t0014g0196a0001c0001t0014g0201 | 4 | NA18939.hp1 NA18952.hp1 NA18953.hp1 others(1): Show |
intron_variant | MODIFIER | c.2798-17052A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57707560 | ||||||
chr13:57707810
|
C | T | 1 | a0001c0001t0001g0059 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2798-16802C>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57707810 | ||||||
chr13:57707870
|
C | A | 4 | a0001c0001t0005g0124a0001c0001t0005g0126a0001c0001t0005g0131others(1): Show | 4 | HG02615.hp2 HG03225.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.2798-16742C>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57707870 | ||||||
chr13:57707901
|
T | A | 107 | a0001c0001t0002g0005a0001c0001t0002g0068a0001c0001t0002g0080others(104): Show | 110 | HG00544.hp1 HG00544.hp2 HG00597.hp1 others(107): Show |
intron_variant | MODIFIER | c.2798-16711T>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57707901 | ||||||
chr13:57708132
|
A | G | 1 | a0001c0001t0008g0024 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.2798-16480A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57708132 | ||||||
chr13:57708156
|
A | G | 1 | a0001c0001t0003g0296 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.2798-16456A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57708156 | ||||||
chr13:57708306
|
G | C | 1 | a0001c0001t0002g0008 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2798-16306G>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57708306 | ||||||
chr13:57708389
|
T | C | 8 | a0001c0001t0001g0161a0001c0001t0003g0011a0001c0001t0007g0078others(5): Show | 8 | HG00323.hp1 HG00558.hp1 HG00735.hp1 others(5): Show |
intron_variant | MODIFIER | c.2798-16223T>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57708389 | ||||||
chr13:57708518
|
G | C | 2 | a0001c0001t0018g0060a0001c0001t0018g0203 | 2 | HG02055.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.2798-16094G>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57708518 | ||||||
chr13:57708578
|
G | A | 114 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(111): Show | 115 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(112): Show |
intron_variant | MODIFIER | c.2798-16034G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57708578 | ||||||
chr13:57708597
|
T | G | 1 | a0001c0001t0003g0296 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.2798-16015T>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57708597 | ||||||
chr13:57708832
|
T | C | 95 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(92): Show | 96 | HG00140.hp1 HG00280.hp1 HG00558.hp2 others(93): Show |
intron_variant | MODIFIER | c.2798-15780T>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57708832 | ||||||
chr13:57709031
|
C | T | 1 | a0001c0001t0002g0205 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.2798-15581C>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57709031 | ||||||
chr13:57709075
|
A | T | 2 | a0001c0001t0007g0180a0001c0001t0007g0181 | 2 | NA18998.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.2798-15537A>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57709075 | ||||||
chr13:57709110
|
A | AAT | 113 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(110): Show | 114 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(111): Show |
intron_variant | MODIFIER | c.2798-15489_2798-15 others(8): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr13 | 57709110 | |||||
chr13:57709443
|
T | C | 1 | a0001c0001t0003g0151 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.2798-15169T>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57709443 | ||||||
chr13:57709925
|
T | C | 1 | a0001c0001t0001g0115 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.2798-14687T>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57709925 | ||||||
chr13:57710251
|
T | C | 1 | a0001c0001t0044g0230 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2798-14361T>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57710251 | ||||||
chr13:57710425
|
A | T | 1 | a0001c0001t0024g0222 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.2798-14187A>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57710425 | ||||||
chr13:57710478
|
T | A | 96 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(93): Show | 97 | HG00140.hp1 HG00280.hp1 HG00558.hp2 others(94): Show |
intron_variant | MODIFIER | c.2798-14134T>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57710478 | ||||||
chr13:57710554
|
A | T | 20 | a0001c0001t0002g0089a0001c0001t0002g0091a0001c0001t0002g0098others(17): Show | 20 | HG01496.hp1 HG01891.hp1 HG02280.hp1 others(17): Show |
intron_variant | MODIFIER | c.2798-14058A>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57710554 | ||||||
chr13:57710595
|
A | G | 1 | a0001c0001t0046g0095 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2798-14017A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57710595 | ||||||
chr13:57710611
|
C | G | 1 | a0001c0001t0001g0129 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.2798-14001C>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57710611 | ||||||
chr13:57710612
|
G | A | 1 | a0001c0001t0009g0029 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.2798-14000G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57710612 | ||||||
chr13:57710663
|
GATTGGTT others(5): Show |
G | 1 | a0001c0001t0046g0095 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2798-13946_2798-13 others(18): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr13 | 57710663 | |||||
chr13:57710767
|
T | C | 25 | a0001c0001t0002g0266a0001c0001t0006g0016a0001c0001t0006g0058others(22): Show | 25 | HG00140.hp2 HG01069.hp2 HG01106.hp2 others(22): Show |
intron_variant | MODIFIER | c.2798-13845T>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57710767 | ||||||
chr13:57710889
|
C | T | 1 | a0001c0001t0002g0235 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.2798-13723C>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57710889 | ||||||
chr13:57710974
|
A | C | 1 | a0001c0001t0006g0058 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.2798-13638A>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57710974 | ||||||
chr13:57711006
|
G | C | 95 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(92): Show | 96 | HG00140.hp1 HG00280.hp1 HG00558.hp2 others(93): Show |
intron_variant | MODIFIER | c.2798-13606G>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57711006 | ||||||
chr13:57711203
|
C | G | 3 | a0001c0001t0001g0139a0001c0001t0010g0090a0001c0001t0010g0274 | 3 | HG01255.hp1 HG03041.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.2798-13409C>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57711203 | ||||||
chr13:57711213
|
C | A | 6 | a0001c0001t0002g0009a0001c0001t0002g0086a0001c0001t0002g0097others(3): Show | 6 | HG01109.hp1 HG02572.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.2798-13399C>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57711213 | ||||||
chr13:57711318
|
A | T | 16 | a0001c0001t0001g0065a0001c0001t0001g0066a0001c0001t0001g0076others(13): Show | 16 | HG00140.hp1 HG00639.hp2 HG00738.hp2 others(13): Show |
intron_variant | MODIFIER | c.2798-13294A>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57711318 | ||||||
chr13:57711395
|
C | T | 1 | a0001c0001t0047g0099 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.2798-13217C>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57711395 | ||||||
chr13:57711664
|
A | G | 1 | a0001c0001t0002g0140 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2798-12948A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57711664 | ||||||
chr13:57711774
|
GAAT | G | 24 | a0001c0001t0006g0016a0001c0001t0006g0058a0001c0001t0006g0083others(21): Show | 24 | HG00140.hp2 HG01069.hp2 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.2798-12830_2798-12 others(9): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr13 | 57711774 | |||||
chr13:57711782
|
A | G | 89 | a0001c0001t0002g0005a0001c0001t0002g0068a0001c0001t0002g0080others(86): Show | 92 | HG00544.hp1 HG00544.hp2 HG00597.hp1 others(89): Show |
intron_variant | MODIFIER | c.2798-12830A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57711782 | ||||||
chr13:57711801
|
A | C | 1 | a0001c0001t0024g0222 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.2798-12811A>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57711801 | ||||||
chr13:57711851
|
A | G | 69 | a0001c0001t0002g0005a0001c0001t0002g0068a0001c0001t0002g0080others(66): Show | 70 | HG00544.hp1 HG00544.hp2 HG00597.hp1 others(67): Show |
intron_variant | MODIFIER | c.2798-12761A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57711851 | ||||||
chr13:57711861
|
T | A | 1 | a0001c0001t0001g0150 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.2798-12751T>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57711861 | ||||||
chr13:57711868
|
G | A | 1 | a0001c0001t0003g0011 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.2798-12744G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57711868 | ||||||
chr13:57712015
|
G | T | 1 | a0001c0003t0002g0297 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.2798-12597G>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57712015 | ||||||
chr13:57712040
|
C | T | 1 | a0001c0001t0001g0010 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.2798-12572C>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57712040 | ||||||
chr13:57712521
|
C | T | 1 | a0001c0001t0044g0230 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2798-12091C>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57712521 | ||||||
chr13:57712679
|
A | G | 1 | a0001c0001t0004g0137 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.2798-11933A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57712679 | ||||||
chr13:57713279
|
A | T | 7 | a0001c0001t0004g0303a0001c0001t0005g0122a0001c0001t0005g0123others(4): Show | 7 | HG02280.hp2 HG02615.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.2798-11333A>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57713279 | ||||||
chr13:57713484
|
G | T | 5 | a0001c0001t0002g0240a0001c0001t0004g0082a0001c0001t0005g0239others(2): Show | 5 | HG02027.hp2 NA18942.hp1 NA18988.hp2 others(2): Show |
intron_variant | MODIFIER | c.2798-11128G>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57713484 | ||||||
chr13:57713804
|
G | A | 2 | a0001c0001t0015g0013a0001c0001t0015g0015 | 2 | HG02615.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.2798-10808G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57713804 | ||||||
chr13:57714227
|
T | C | 1 | a0001c0001t0002g0234 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2798-10385T>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57714227 | ||||||
chr13:57714368
|
T | C | 261 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(258): Show | 265 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(262): Show |
intron_variant | MODIFIER | c.2798-10244T>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57714368 | ||||||
chr13:57714704
|
G | A | 1 | a0001c0001t0002g0205 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.2798-9908G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57714704 | ||||||
chr13:57714746
|
T | C | 201 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(198): Show | 205 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(202): Show |
intron_variant | MODIFIER | c.2798-9866T>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57714746 | ||||||
chr13:57714788
|
G | A | 7 | a0001c0001t0002g0128a0001c0001t0002g0140a0001c0001t0034g0247others(4): Show | 7 | HG02257.hp1 HG02257.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.2798-9824G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57714788 | ||||||
chr13:57714924
|
A | T | 1 | a0001c0001t0002g0298 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2798-9688A>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57714924 | ||||||
chr13:57714994
|
A | G | 1 | a0008c0007t0006g0206 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.2798-9618A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57714994 | ||||||
chr13:57714998
|
T | C | 1 | a0001c0001t0003g0070 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.2798-9614T>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57714998 | ||||||
chr13:57715026
|
G | A | 1 | a0001c0001t0004g0199 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.2798-9586G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57715026 | ||||||
chr13:57715096
|
G | A | 10 | a0001c0001t0004g0085a0001c0001t0012g0043a0001c0001t0012g0044others(7): Show | 10 | NA18942.hp2 NA18962.hp1 NA18990.hp1 others(7): Show |
intron_variant | MODIFIER | c.2798-9516G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57715096 | ||||||
chr13:57715153
|
A | G | 1 | a0006c0009t0007g0293 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.2798-9459A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57715153 | ||||||
chr13:57715211
|
A | G | 1 | a0001c0011t0001g0214 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.2798-9401A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57715211 | ||||||
chr13:57715402
|
GAGTGTGT others(38): Show |
G | 1 | a0001c0001t0005g0147 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2798-9206_2798-916 others(49): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr13 | 57715402 | |||||
chr13:57715452
|
T | A | 17 | a0001c0001t0001g0161a0001c0001t0002g0008a0001c0001t0002g0009others(14): Show | 17 | HG00323.hp1 HG00558.hp1 HG00735.hp1 others(14): Show |
intron_variant | MODIFIER | c.2798-9160T>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57715452 | ||||||
chr13:57715546
|
A | T | 7 | a0001c0001t0004g0303a0001c0001t0005g0122a0001c0001t0005g0123others(4): Show | 7 | HG02280.hp2 HG02615.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.2798-9066A>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57715546 | ||||||
chr13:57715641
|
C | A | 30 | a0001c0001t0004g0303a0001c0001t0005g0122a0001c0001t0005g0123others(27): Show | 30 | HG00140.hp2 HG01069.hp2 HG01106.hp2 others(27): Show |
intron_variant | MODIFIER | c.2798-8971C>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57715641 | ||||||
chr13:57715671
|
T | G | 3 | a0001c0001t0004g0092a0001c0001t0005g0147a0001c0001t0042g0279 | 3 | HG01891.hp2 HG02451.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.2798-8941T>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57715671 | ||||||
chr13:57715910
|
T | G | 3 | a0001c0001t0002g0089a0001c0001t0002g0091a0001c0001t0002g0098 | 3 | HG02630.hp2 HG02818.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.2798-8702T>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57715910 | ||||||
chr13:57715947
|
T | G | 5 | a0001c0001t0002g0138a0001c0001t0002g0141a0001c0001t0002g0142others(2): Show | 5 | HG02622.hp2 HG02809.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.2798-8665T>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57715947 | ||||||
chr13:57715957
|
A | G | 5 | a0001c0001t0004g0092a0001c0001t0004g0136a0001c0001t0004g0148others(2): Show | 5 | HG01884.hp2 HG01891.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.2798-8655A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57715957 | ||||||
chr13:57716349
|
G | A | 1 | a0001c0001t0001g0115 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.2798-8263G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57716349 | ||||||
chr13:57716427
|
T | A | 1 | a0001c0001t0030g0039 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.2798-8185T>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57716427 | ||||||
chr13:57717024
|
G | T | 1 | a0001c0001t0008g0024 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.2798-7588G>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57717024 | ||||||
chr13:57717097
|
T | C | 1 | a0001c0001t0007g0116 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.2798-7515T>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57717097 | ||||||
chr13:57717192
|
A | G | 70 | a0001c0001t0002g0005a0001c0001t0002g0068a0001c0001t0002g0080others(67): Show | 71 | HG00544.hp1 HG00544.hp2 HG00597.hp1 others(68): Show |
intron_variant | MODIFIER | c.2798-7420A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57717192 | ||||||
chr13:57717214
|
G | A | 1 | a0001c0001t0007g0121 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.2798-7398G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57717214 | ||||||
chr13:57717487
|
G | A | 262 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(259): Show | 266 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.2798-7125G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57717487 | ||||||
chr13:57717528
|
C | T | 19 | a0001c0001t0006g0016a0001c0001t0006g0058a0001c0001t0006g0083others(16): Show | 19 | HG00140.hp2 HG01069.hp2 HG01106.hp2 others(16): Show |
intron_variant | MODIFIER | c.2798-7084C>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57717528 | ||||||
chr13:57717564
|
C | T | 7 | a0001c0001t0001g0161a0001c0001t0003g0011a0001c0001t0007g0078others(4): Show | 7 | HG00323.hp1 HG00558.hp1 HG00735.hp1 others(4): Show |
intron_variant | MODIFIER | c.2798-7048C>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57717564 | ||||||
chr13:57717658
|
G | A | 17 | a0001c0001t0001g0161a0001c0001t0002g0008a0001c0001t0002g0009others(14): Show | 17 | HG00323.hp1 HG00558.hp1 HG00735.hp1 others(14): Show |
intron_variant | MODIFIER | c.2798-6954G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57717658 | ||||||
chr13:57717661
|
G | A | 1 | a0001c0001t0001g0059 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2798-6951G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57717661 | ||||||
chr13:57717742
|
G | A | 5 | a0001c0001t0005g0132a0001c0001t0005g0275a0001c0001t0005g0276others(2): Show | 5 | HG01496.hp1 HG02451.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.2798-6870G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57717742 | ||||||
chr13:57717772
|
A | C | 1 | a0001c0001t0006g0083 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.2798-6840A>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57717772 | ||||||
chr13:57718073
|
A | C | 1 | a0001c0001t0017g0152 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.2798-6539A>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57718073 | ||||||
chr13:57718146
|
A | G | 2 | a0001c0001t0013g0018a0001c0001t0013g0022 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.2798-6466A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57718146 | ||||||
chr13:57718182
|
C | T | 1 | a0001c0001t0034g0247 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2798-6430C>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57718182 | ||||||
chr13:57718725
|
A | G | 1 | a0001c0001t0015g0014 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2798-5887A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57718725 | ||||||
chr13:57719037
|
T | G | 2 | a0001c0001t0002g0086a0001c0001t0002g0097 | 2 | HG01109.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.2798-5575T>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57719037 | ||||||
chr13:57719153
|
C | T | 1 | a0001c0001t0002g0009 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2798-5459C>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57719153 | ||||||
chr13:57719400
|
T | C | 7 | a0001c0001t0001g0161a0001c0001t0003g0011a0001c0001t0007g0078others(4): Show | 7 | HG00323.hp1 HG00558.hp1 HG00735.hp1 others(4): Show |
intron_variant | MODIFIER | c.2798-5212T>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57719400 | ||||||
chr13:57719475
|
C | T | 5 | a0001c0001t0003g0164a0001c0001t0003g0165a0001c0001t0008g0019others(2): Show | 5 | HG00738.hp1 HG01069.hp1 HG01099.hp1 others(2): Show |
intron_variant | MODIFIER | c.2798-5137C>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57719475 | ||||||
chr13:57719724
|
A | G | 3 | a0001c0001t0001g0258a0001c0001t0001g0281a0001c0001t0001g0282 | 3 | NA18945.hp1 NA18984.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.2798-4888A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57719724 | ||||||
chr13:57719863
|
T | A | 4 | a0001c0001t0003g0164a0001c0001t0003g0165a0001c0001t0008g0019others(1): Show | 4 | HG00738.hp1 HG01099.hp1 HG01257.hp1 others(1): Show |
intron_variant | MODIFIER | c.2798-4749T>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57719863 | ||||||
chr13:57720234
|
A | C | 7 | a0001c0001t0004g0303a0001c0001t0005g0122a0001c0001t0005g0123others(4): Show | 7 | HG02280.hp2 HG02615.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.2798-4378A>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57720234 | ||||||
chr13:57720239
|
C | A | 2 | a0001c0001t0018g0060a0001c0001t0018g0203 | 2 | HG02055.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.2798-4373C>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57720239 | ||||||
chr13:57720493
|
T | C | 5 | a0001c0001t0002g0128a0001c0001t0002g0140a0001c0001t0037g0012others(2): Show | 5 | HG02257.hp1 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.2798-4119T>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57720493 | ||||||
chr13:57720495
|
A | G | 21 | a0001c0001t0002g0089a0001c0001t0002g0091a0001c0001t0002g0098others(18): Show | 21 | HG01243.hp2 HG01496.hp1 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.2798-4117A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57720495 | ||||||
chr13:57720676
|
A | C | 2 | a0001c0001t0018g0060a0001c0001t0018g0203 | 2 | HG02055.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.2798-3936A>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57720676 | ||||||
chr13:57720721
|
T | A | 1 | a0001c0001t0005g0147 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2798-3891T>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57720721 | ||||||
chr13:57720722
|
A | T | 1 | a0001c0001t0005g0147 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2798-3890A>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57720722 | ||||||
chr13:57720773
|
T | TGGGGGGG others(38): Show |
1 | a0001c0001t0005g0147 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2798-3837_2798-383 others(49): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr13 | 57720773 | |||||
chr13:57720869
|
A | G | 1 | a0001c0001t0003g0246 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.2798-3743A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57720869 | ||||||
chr13:57721369
|
T | C | 1 | a0001c0001t0034g0247 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2798-3243T>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57721369 | ||||||
chr13:57721373
|
GTATATAT others(4): Show |
G | 3 | a0001c0001t0002g0089a0001c0001t0002g0091a0001c0001t0002g0098 | 3 | HG02630.hp2 HG02818.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.2798-3233_2798-322 others(15): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr13 | 57721373 | |||||
chr13:57721391
|
C | A | 1 | a0001c0001t0003g0069 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.2798-3221C>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57721391 | ||||||
chr13:57721474
|
C | T | 1 | a0001c0001t0015g0014 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2798-3138C>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57721474 | ||||||
chr13:57721492
|
A | G | 2 | a0001c0001t0002g0086a0001c0001t0002g0097 | 2 | HG01109.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.2798-3120A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57721492 | ||||||
chr13:57721579
|
C | A | 1 | a0001c0001t0001g0218 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.2798-3033C>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57721579 | ||||||
chr13:57721975
|
G | C | 1 | a0001c0001t0023g0176 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.2798-2637G>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57721975 | ||||||
chr13:57722071
|
T | C | 112 | a0001c0001t0002g0005a0001c0001t0002g0068a0001c0001t0002g0080others(109): Show | 115 | HG00323.hp1 HG00544.hp1 HG00544.hp2 others(112): Show |
intron_variant | MODIFIER | c.2798-2541T>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57722071 | ||||||
chr13:57722084
|
T | A | 1 | a0001c0001t0002g0145 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2798-2528T>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57722084 | ||||||
chr13:57722089
|
A | T | 2 | a0001c0001t0018g0060a0001c0001t0018g0203 | 2 | HG02055.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.2798-2523A>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57722089 | ||||||
chr13:57722118
|
G | A | 1 | a0001c0001t0006g0242 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.2798-2494G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57722118 | ||||||
chr13:57722145
|
C | T | 1 | a0006c0009t0007g0293 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.2798-2467C>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57722145 | ||||||
chr13:57722340
|
A | G | 2 | a0001c0001t0016g0265a0001c0005t0028g0052 | 2 | HG02080.hp1 HG02083.hp1 |
intron_variant | MODIFIER | c.2798-2272A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57722340 | ||||||
chr13:57722355
|
T | C | 1 | a0001c0011t0001g0214 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.2798-2257T>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57722355 | ||||||
chr13:57722456
|
T | C | 1 | a0001c0001t0002g0162 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.2798-2156T>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57722456 | ||||||
chr13:57722588
|
A | T | 22 | a0001c0001t0006g0016a0001c0001t0006g0058a0001c0001t0006g0083others(19): Show | 22 | HG00140.hp2 HG01069.hp2 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.2798-2024A>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57722588 | ||||||
chr13:57722602
|
C | T | 1 | a0001c0001t0004g0117 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.2798-2010C>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57722602 | ||||||
chr13:57722741
|
G | A | 7 | a0001c0001t0001g0238a0001c0001t0001g0258a0001c0001t0001g0281others(4): Show | 7 | NA18945.hp1 NA18984.hp1 NA18988.hp1 others(4): Show |
intron_variant | MODIFIER | c.2798-1871G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57722741 | ||||||
chr13:57722963
|
A | T | 1 | a0001c0001t0034g0247 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2798-1649A>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57722963 | ||||||
chr13:57723025
|
C | T | 6 | a0001c0001t0005g0132a0001c0001t0005g0147a0001c0001t0005g0275others(3): Show | 6 | HG01496.hp1 HG02451.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.2798-1587C>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57723025 | ||||||
chr13:57723033
|
C | T | 3 | a0001c0001t0014g0004a0001c0001t0014g0196a0001c0001t0014g0201 | 4 | NA18939.hp1 NA18952.hp1 NA18953.hp1 others(1): Show |
intron_variant | MODIFIER | c.2798-1579C>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57723033 | ||||||
chr13:57723133
|
A | G | 1 | a0001c0001t0044g0230 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2798-1479A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57723133 | ||||||
chr13:57723267
|
T | TA | 255 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(252): Show | 259 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(256): Show |
intron_variant | MODIFIER | c.2798-1340dupA | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr13 | 57723267 | |||||
chr13:57723419
|
A | T | 6 | a0001c0001t0005g0132a0001c0001t0005g0147a0001c0001t0005g0275others(3): Show | 6 | HG01496.hp1 HG02451.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.2798-1193A>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57723419 | ||||||
chr13:57723420
|
A | G | 1 | a0001c0001t0001g0185 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.2798-1192A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57723420 | ||||||
chr13:57723422
|
G | A | 38 | a0001c0001t0002g0240a0001c0001t0002g0298a0001c0001t0004g0003others(35): Show | 40 | HG00597.hp2 HG01243.hp1 HG01256.hp1 others(37): Show |
intron_variant | MODIFIER | c.2798-1190G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57723422 | ||||||
chr13:57723682
|
C | A | 256 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(253): Show | 260 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(257): Show |
intron_variant | MODIFIER | c.2798-930C>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57723682 | ||||||
chr13:57723907
|
C | T | 1 | a0001c0001t0002g0301 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2798-705C>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57723907 | ||||||
chr13:57723909
|
T | A | 1 | a0001c0001t0008g0017 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.2798-703T>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57723909 | ||||||
chr13:57723937
|
C | T | 1 | a0001c0001t0001g0197 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.2798-675C>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57723937 | ||||||
chr13:57723973
|
T | C | 3 | a0001c0001t0002g0128a0001c0001t0002g0140a0001c0001t0037g0012 | 3 | HG02486.hp2 HG02572.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.2798-639T>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57723973 | ||||||
chr13:57724029
|
G | A | 1 | a0001c0001t0006g0083 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.2798-583G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57724029 | ||||||
chr13:57724043
|
C | T | 1 | a0001c0001t0002g0234 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2798-569C>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57724043 | ||||||
chr13:57724277
|
A | G | 107 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(104): Show | 108 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(105): Show |
intron_variant | MODIFIER | c.2798-335A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57724277 |