geneid | 51098 |
---|---|
ensemblid | ENSG00000101052.13 |
hgncid | 15901 |
symbol | IFT52 |
name | intraflagellar transport 52 |
refseq_nuc | NM_016004.5 |
refseq_prot | NP_057088.2 |
ensembl_nuc | ENST00000373030.8 |
ensembl_prot | ENSP00000362121.3 |
mane_status | MANE Select |
chr | chr20 |
start | 43590937 |
end | 43647299 |
strand | + |
ver | v1.2 |
region | chr20:43590937-43647299 |
region5000 | chr20:43585937-43652299 |
regionname0 | IFT52_chr20_43590937_43647299 |
regionname5000 | IFT52_chr20_43585937_43652299 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 437 | 295 | 77 | 64 | 106 | 10 | 36 | 80 | IFT52_chr20_43585937_43652299 | IFT52 | copy fasta | chr20 | 43585937 | 43652299 |
a0002 | 0/0 | 437 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | copy fasta | chr20 | 43585937 | 43652299 |
a0003 | 0/0 | 437 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | copy fasta | chr20 | 43585937 | 43652299 |
a0004 | 0/0 | 437 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | copy fasta | chr20 | 43585937 | 43652299 |
a0005 | 0/0 | 437 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | copy fasta | chr20 | 43585937 | 43652299 |
a0006 | 0/0 | 437 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | copy fasta | chr20 | 43585937 | 43652299 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/0 | 1314 | 179 | 44 | 45 | 56 | 10 | 24 | IFT52_chr20_43585937_43652299 | IFT52 | copy fasta | chr20 | 43585937 | 43652299 |
c0002 | 1/1 | 1314 | 109 | 27 | 18 | 50 | 0 | 12 | IFT52_chr20_43585937_43652299 | IFT52 | copy fasta | chr20 | 43585937 | 43652299 |
c0003 | 0/0 | 1314 | 6 | 5 | 1 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | copy fasta | chr20 | 43585937 | 43652299 |
c0004 | 0/0 | 1314 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | copy fasta | chr20 | 43585937 | 43652299 |
c0005 | 0/0 | 1314 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | copy fasta | chr20 | 43585937 | 43652299 |
c0006 | 0/0 | 1314 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | copy fasta | chr20 | 43585937 | 43652299 |
c0007 | 0/0 | 1314 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | copy fasta | chr20 | 43585937 | 43652299 |
c0008 | 0/0 | 1314 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | copy fasta | chr20 | 43585937 | 43652299 |
c0009 | 0/0 | 1314 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | copy fasta | chr20 | 43585937 | 43652299 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 441 | 298 | 79 | 64 | 107 | 10 | 36 | IFT52_chr20_43585937_43652299 | IFT52 | copy fasta | chr20 | 43585937 | 43652299 |
t0002 | 0/0 | 441 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | copy fasta | chr20 | 43585937 | 43652299 |
t0003 | 0/0 | 441 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | copy fasta | chr20 | 43585937 | 43652299 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0002 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0003 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0007 | 1/0 | 2 | 0 | 1 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0010 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0014 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0050 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0164 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0183 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0200 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0206 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 1314 | 179 | 44 | 45 | 56 | 10 | 24 | IFT52_chr20_43585937_43652299 | IFT52 | copy fasta | chr20 | 43585937 | 43652299 |
a0001c0002 | 1/1 | 1314 | 109 | 27 | 18 | 50 | 0 | 12 | IFT52_chr20_43585937_43652299 | IFT52 | copy fasta | chr20 | 43585937 | 43652299 |
a0001c0003 | 0/0 | 1314 | 6 | 5 | 1 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | copy fasta | chr20 | 43585937 | 43652299 |
a0001c0006 | 0/0 | 1314 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | copy fasta | chr20 | 43585937 | 43652299 |
a0002c0009 | 0/0 | 1314 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | copy fasta | chr20 | 43585937 | 43652299 |
a0003c0008 | 0/0 | 1314 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | copy fasta | chr20 | 43585937 | 43652299 |
a0004c0005 | 0/0 | 1314 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | copy fasta | chr20 | 43585937 | 43652299 |
a0005c0007 | 0/0 | 1314 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | copy fasta | chr20 | 43585937 | 43652299 |
a0006c0004 | 0/0 | 1314 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | copy fasta | chr20 | 43585937 | 43652299 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 1754 | 178 | 44 | 45 | 55 | 10 | 24 | IFT52_chr20_43585937_43652299 | IFT52 | copy fasta | chr20 | 43585937 | 43652299 |
a0001c0001t0002 | 0/0 | 1754 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | copy fasta | chr20 | 43585937 | 43652299 |
a0001c0002t0001 | 1/1 | 1754 | 109 | 27 | 18 | 50 | 0 | 12 | IFT52_chr20_43585937_43652299 | IFT52 | copy fasta | chr20 | 43585937 | 43652299 |
a0001c0003t0001 | 0/0 | 1754 | 6 | 5 | 1 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | copy fasta | chr20 | 43585937 | 43652299 |
a0001c0006t0001 | 0/0 | 1754 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | copy fasta | chr20 | 43585937 | 43652299 |
a0002c0009t0001 | 0/0 | 1754 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | copy fasta | chr20 | 43585937 | 43652299 |
a0003c0008t0001 | 0/0 | 1754 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | copy fasta | chr20 | 43585937 | 43652299 |
a0004c0005t0003 | 0/0 | 1754 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | copy fasta | chr20 | 43585937 | 43652299 |
a0005c0007t0001 | 0/0 | 1754 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | copy fasta | chr20 | 43585937 | 43652299 |
a0006c0004t0001 | 0/0 | 1754 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | copy fasta | chr20 | 43585937 | 43652299 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0003 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0001t0001g0014 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0001t0001g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0001t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0001t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0001t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0001t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0001t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0001t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0001t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0001t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0001t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0001t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0001t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0001t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0001t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0001t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0001t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0001t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0001t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0001t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0001t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0002t0001g0001 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0002t0001g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0002t0001g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0002t0001g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0002t0001g0007 | 1/0 | 2 | 0 | 1 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0002t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0002t0001g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0002t0001g0010 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0002t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0002t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0002t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0002t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0002t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0002t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0002t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0002t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0002t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0002t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0002t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0002t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0002t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0002t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0002t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0002t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0002t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0002t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0002t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0002t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0002t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0002t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0002t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0002t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0002t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0002t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0002t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0002t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0002t0001g0050 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0002t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0002t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0002t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0002t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0002t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0002t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0002t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0002t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0002t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0002t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0002t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0002t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0002t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0002t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0002t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0002t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0002t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0002t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0002t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0002t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0002t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0002t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0002t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0002t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0002t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0002t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0002t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0002t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0002t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0002t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0002t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0002t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0002t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0002t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0002t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0002t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0002t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0002t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0002t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0002t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0002t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0002t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0002t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0002t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0002t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0003t0001g0002 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0003t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0003t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0003t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0001c0006t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0002c0009t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0003c0008t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0004c0005t0003g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0005c0007t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
a0006c0004t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0177 | EUR | GBR | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0183 | EUR | GBR | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0164 | EUR | FIN | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0161 | EUR | FIN | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0159 | EUR | FIN | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0206 | EUR | FIN | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | CHS | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | CHS | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0268 | EAS | CHS | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
HG00544 | hp2 | a0001 | c0002 | t0001 | g0066 | EAS | CHS | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | CHS | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | CHS | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
HG00642 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | PUR | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0147 | AMR | PUR | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0131 | AMR | PUR | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0160 | AMR | PUR | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0138 | AMR | PUR | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
HG00735 | hp2 | a0001 | c0002 | t0001 | g0238 | AMR | PUR | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0113 | AMR | PUR | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0250 | AMR | PUR | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0149 | AMR | PUR | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0279 | AMR | PUR | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0142 | AMR | PUR | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0176 | AMR | PUR | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0195 | AMR | PUR | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0143 | AMR | PUR | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0144 | AMR | PUR | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0203 | AMR | PUR | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
HG01081 | hp1 | a0001 | c0002 | t0001 | g0105 | AMR | PUR | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0214 | AMR | PUR | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
HG01099 | hp1 | a0001 | c0002 | t0001 | g0044 | AMR | PUR | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0184 | AMR | PUR | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0136 | AMR | PUR | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0156 | AMR | PUR | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0114 | AMR | PUR | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
HG01109 | hp2 | a0001 | c0002 | t0001 | g0028 | AMR | PUR | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0236 | AMR | PUR | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0277 | AMR | PUR | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0115 | AMR | PUR | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
HG01168 | hp2 | a0001 | c0002 | t0001 | g0081 | AMR | PUR | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0244 | AMR | PUR | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0237 | AMR | PUR | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
HG01175 | hp1 | a0001 | c0002 | t0001 | g0052 | AMR | PUR | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0243 | AMR | PUR | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0151 | AMR | PUR | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
HG01192 | hp2 | a0001 | c0002 | t0001 | g0007 | AMR | PUR | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0273 | AMR | PUR | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0258 | AMR | PUR | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
HG01257 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | CLM | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0148 | AMR | CLM | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0275 | AMR | CLM | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0233 | AMR | CLM | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
HG01346 | hp1 | a0001 | c0002 | t0001 | g0048 | AMR | CLM | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | CLM | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0134 | AMR | CLM | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
HG01361 | hp2 | a0001 | c0003 | t0001 | g0023 | AMR | CLM | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
HG01433 | hp1 | a0001 | c0002 | t0001 | g0080 | AMR | CLM | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0223 | AMR | CLM | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
HG01496 | hp1 | a0001 | c0002 | t0001 | g0062 | AMR | CLM | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0234 | AMR | CLM | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
HG01884 | hp1 | a0001 | c0002 | t0001 | g0017 | AFR | ACB | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0230 | AFR | ACB | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0276 | AFR | ACB | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0154 | AFR | ACB | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0271 | AMR | PEL | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
HG01934 | hp2 | a0001 | c0002 | t0001 | g0060 | AMR | PEL | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0110 | AMR | PEL | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
HG01952 | hp2 | a0001 | c0002 | t0001 | g0056 | AMR | PEL | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
HG01981 | hp1 | a0001 | c0002 | t0001 | g0057 | AMR | PEL | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0187 | AMR | PEL | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
HG01993 | hp1 | a0001 | c0002 | t0001 | g0047 | AMR | PEL | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0185 | AMR | PEL | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
HG02027 | hp1 | a0001 | c0002 | t0001 | g0065 | EAS | KHV | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | KHV | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | KHV | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | KHV | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0123 | AFR | ACB | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0259 | AFR | ACB | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
HG02056 | hp1 | a0003 | c0008 | t0001 | g0034 | EAS | KHV | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
HG02056 | hp2 | a0001 | c0002 | t0001 | g0064 | EAS | KHV | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | KHV | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
HG02071 | hp2 | a0001 | c0002 | t0001 | g0075 | EAS | KHV | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0264 | EAS | KHV | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | KHV | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | KHV | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
HG02083 | hp2 | a0005 | c0007 | t0001 | g0095 | EAS | KHV | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | KHV | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
HG02129 | hp2 | a0001 | c0002 | t0001 | g0070 | EAS | KHV | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | KHV | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | KHV | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
HG02135 | hp1 | a0001 | c0002 | t0001 | g0038 | EAS | KHV | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
HG02135 | hp2 | a0001 | c0002 | t0001 | g0027 | EAS | KHV | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0232 | AFR | ACB | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0158 | AFR | ACB | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0218 | AMR | PEL | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
HG02148 | hp2 | a0001 | c0002 | t0001 | g0053 | AMR | PEL | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | CDX | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
HG02165 | hp2 | a0001 | c0002 | t0001 | g0069 | EAS | CDX | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
HG02257 | hp1 | a0001 | c0002 | t0001 | g0042 | AFR | ACB | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0231 | AFR | ACB | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
HG02258 | hp1 | a0001 | c0002 | t0001 | g0041 | AFR | ACB | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0249 | AFR | ACB | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0266 | AFR | ACB | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0150 | AFR | ACB | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
HG02300 | hp1 | a0001 | c0002 | t0001 | g0046 | AMR | PEL | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0179 | AMR | PEL | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0248 | AFR | GWD | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
HG02572 | hp2 | a0001 | c0002 | t0001 | g0122 | AFR | GWD | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
HG02602 | hp1 | a0001 | c0002 | t0001 | g0072 | SAS | PJL | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
HG02602 | hp2 | a0001 | c0002 | t0001 | g0108 | SAS | PJL | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
HG02615 | hp1 | a0001 | c0002 | t0001 | g0107 | AFR | GWD | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
HG02615 | hp2 | a0001 | c0003 | t0001 | g0002 | AFR | GWD | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0241 | AFR | GWD | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
HG02622 | hp2 | a0001 | c0002 | t0001 | g0240 | AFR | GWD | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0247 | AFR | GWD | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
HG02630 | hp2 | a0001 | c0002 | t0001 | g0018 | AFR | GWD | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0162 | AFR | GWD | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
HG02647 | hp2 | a0001 | c0002 | t0001 | g0091 | AFR | GWD | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
HG02683 | hp1 | a0001 | c0002 | t0001 | g0078 | SAS | PJL | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0242 | SAS | PJL | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0226 | SAS | PJL | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
HG02698 | hp2 | a0001 | c0002 | t0001 | g0076 | SAS | PJL | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
HG02717 | hp1 | a0001 | c0002 | t0001 | g0085 | AFR | GWD | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
HG02717 | hp2 | a0001 | c0002 | t0001 | g0269 | AFR | GWD | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
HG02723 | hp1 | a0001 | c0002 | t0001 | g0009 | AFR | GWD | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
HG02723 | hp2 | a0001 | c0002 | t0001 | g0004 | AFR | GWD | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0245 | SAS | PJL | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0166 | SAS | PJL | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0128 | SAS | PJL | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
HG02738 | hp2 | a0001 | c0002 | t0001 | g0106 | SAS | PJL | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0251 | AFR | GWD | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0124 | AFR | GWD | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0272 | AFR | GWD | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0265 | AFR | GWD | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
HG02886 | hp1 | a0001 | c0002 | t0001 | g0084 | AFR | GWD | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0117 | AFR | GWD | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0262 | AFR | GWD | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0278 | AFR | GWD | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0263 | AFR | GWD | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
HG02896 | hp2 | a0001 | c0002 | t0001 | g0086 | AFR | GWD | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0260 | AFR | GWD | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
HG02897 | hp2 | a0001 | c0002 | t0001 | g0083 | AFR | GWD | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0261 | AFR | ESN | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
HG02922 | hp2 | a0001 | c0003 | t0001 | g0002 | AFR | ESN | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0165 | AFR | ESN | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0281 | AFR | ESN | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
HG02976 | hp1 | a0001 | c0002 | t0001 | g0004 | AFR | ESN | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0270 | AFR | ESN | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0125 | AFR | GWD | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
HG03041 | hp2 | a0001 | c0002 | t0001 | g0024 | AFR | GWD | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
HG03209 | hp1 | a0001 | c0002 | t0001 | g0087 | AFR | MSL | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0118 | AFR | MSL | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0014 | SAS | PJL | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0167 | SAS | PJL | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0157 | AFR | MSL | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0120 | AFR | MSL | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
HG03486 | hp1 | a0001 | c0002 | t0001 | g0082 | AFR | MSL | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0152 | AFR | MSL | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0222 | SAS | PJL | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
HG03491 | hp2 | a0001 | c0002 | t0001 | g0010 | SAS | PJL | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
HG03492 | hp1 | a0001 | c0002 | t0001 | g0010 | SAS | PJL | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0163 | SAS | PJL | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
HG03516 | hp1 | a0001 | c0002 | t0001 | g0040 | AFR | ESN | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0246 | AFR | ESN | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0228 | AFR | GWD | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
HG03540 | hp2 | a0001 | c0003 | t0001 | g0002 | AFR | GWD | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0190 | AFR | MSL | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
HG03579 | hp2 | a0001 | c0002 | t0001 | g0090 | AFR | MSL | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0212 | SAS | PJL | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0146 | SAS | PJL | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0130 | SAS | PJL | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0216 | SAS | PJL | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
HG03704 | hp1 | a0001 | c0002 | t0001 | g0051 | SAS | PJL | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0196 | SAS | PJL | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
HG03834 | hp1 | a0001 | c0002 | t0001 | g0079 | SAS | BEB | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0253 | SAS | BEB | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0141 | SAS | STU | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0140 | SAS | STU | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0169 | SAS | BEB | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0181 | SAS | BEB | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0235 | SAS | STU | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0112 | SAS | STU | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0111 | SAS | STU | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0224 | SAS | STU | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
HG04228 | hp1 | a0001 | c0002 | t0001 | g0104 | SAS | STU | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0211 | SAS | STU | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | CHB | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
NA18612 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | CHB | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
NA18906 | hp1 | a0002 | c0009 | t0001 | g0020 | AFR | YRI | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0153 | AFR | YRI | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
NA18939 | hp2 | a0001 | c0002 | t0001 | g0032 | EAS | JPT | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
NA18941 | hp1 | a0001 | c0002 | t0001 | g0074 | EAS | JPT | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
NA18945 | hp2 | a0001 | c0002 | t0001 | g0008 | EAS | JPT | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
NA18946 | hp1 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
NA18950 | hp2 | a0001 | c0002 | t0001 | g0030 | EAS | JPT | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
NA18951 | hp1 | a0001 | c0002 | t0001 | g0039 | EAS | JPT | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
NA18952 | hp1 | a0001 | c0002 | t0001 | g0100 | EAS | JPT | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
NA18952 | hp2 | a0001 | c0002 | t0001 | g0008 | EAS | JPT | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
NA18954 | hp1 | a0001 | c0002 | t0001 | g0059 | EAS | JPT | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
NA18959 | hp1 | a0001 | c0002 | t0001 | g0043 | EAS | JPT | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
NA18963 | hp1 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
NA18966 | hp1 | a0001 | c0002 | t0001 | g0031 | EAS | JPT | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
NA18968 | hp1 | a0001 | c0002 | t0001 | g0035 | EAS | JPT | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
NA18970 | hp2 | a0001 | c0002 | t0001 | g0071 | EAS | JPT | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
NA18971 | hp1 | a0001 | c0002 | t0001 | g0103 | EAS | JPT | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
NA18972 | hp1 | a0001 | c0002 | t0001 | g0098 | EAS | JPT | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
NA18973 | hp2 | a0001 | c0002 | t0001 | g0073 | EAS | JPT | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
NA18974 | hp1 | a0001 | c0002 | t0001 | g0061 | EAS | JPT | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
NA18975 | hp1 | a0001 | c0002 | t0001 | g0102 | EAS | JPT | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
NA18977 | hp1 | a0001 | c0002 | t0001 | g0045 | EAS | JPT | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
NA18982 | hp1 | a0001 | c0002 | t0001 | g0092 | EAS | JPT | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
NA18982 | hp2 | a0001 | c0002 | t0001 | g0055 | EAS | JPT | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
NA18984 | hp1 | a0001 | c0002 | t0001 | g0006 | EAS | JPT | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
NA18990 | hp2 | a0001 | c0002 | t0001 | g0037 | EAS | JPT | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
NA18994 | hp2 | a0001 | c0002 | t0001 | g0096 | EAS | JPT | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
NA18995 | hp1 | a0001 | c0002 | t0001 | g0029 | EAS | JPT | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
NA18998 | hp1 | a0001 | c0002 | t0001 | g0077 | EAS | JPT | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
NA19000 | hp2 | a0001 | c0002 | t0001 | g0093 | EAS | JPT | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
NA19004 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
NA19009 | hp1 | a0001 | c0002 | t0001 | g0033 | EAS | JPT | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
NA19010 | hp1 | a0001 | c0002 | t0001 | g0068 | EAS | JPT | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0229 | AFR | LWK | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
NA19030 | hp2 | a0001 | c0002 | t0001 | g0019 | AFR | LWK | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0215 | AFR | LWK | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
NA19043 | hp2 | a0001 | c0002 | t0001 | g0089 | AFR | LWK | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
NA19054 | hp2 | a0001 | c0002 | t0001 | g0054 | EAS | JPT | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
NA19055 | hp1 | a0001 | c0002 | t0001 | g0067 | EAS | JPT | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
NA19055 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
NA19063 | hp1 | a0001 | c0002 | t0001 | g0101 | EAS | JPT | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
NA19063 | hp2 | a0001 | c0002 | t0001 | g0063 | EAS | JPT | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
NA19070 | hp1 | a0001 | c0002 | t0001 | g0006 | EAS | JPT | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
NA19083 | hp1 | a0001 | c0002 | t0001 | g0097 | EAS | JPT | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
NA19083 | hp2 | a0001 | c0001 | t0002 | g0170 | EAS | JPT | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
NA19085 | hp1 | a0001 | c0002 | t0001 | g0036 | EAS | JPT | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
NA19088 | hp2 | a0001 | c0002 | t0001 | g0099 | EAS | JPT | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
NA19089 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
NA19089 | hp2 | a0001 | c0002 | t0001 | g0026 | EAS | JPT | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
NA19240 | hp1 | a0001 | c0002 | t0001 | g0009 | AFR | YRI | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
NA19240 | hp2 | a0001 | c0003 | t0001 | g0021 | AFR | YRI | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
NA20129 | hp1 | a0006 | c0004 | t0001 | g0186 | AFR | ASW | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | ASW | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0003 | EUR | TSI | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0168 | EUR | TSI | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0200 | EUR | TSI | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0145 | EUR | TSI | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
NA20905 | hp1 | a0001 | c0002 | t0001 | g0094 | SAS | GIH | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
NA20905 | hp2 | a0001 | c0002 | t0001 | g0049 | SAS | GIH | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0217 | AMR | CLM | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | CLM | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0280 | AFR | ACB | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
HG02109 | hp2 | a0001 | c0002 | t0001 | g0239 | AFR | ACB | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0119 | AFR | ACB | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
HG02486 | hp2 | a0001 | c0002 | t0001 | g0088 | AFR | ACB | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0274 | AFR | USA | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0255 | AFR | USA | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
NA18955 | hp2 | a0001 | c0002 | t0001 | g0025 | EAS | JPT | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
NA20300 | hp1 | a0001 | c0002 | t0001 | g0058 | AFR | USA | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
NA20300 | hp2 | a0001 | c0003 | t0001 | g0022 | AFR | USA | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
NA21309 | hp1 | a0004 | c0005 | t0003 | g0155 | AFR | LWK | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
NA21309 | hp2 | a0001 | c0006 | t0001 | g0016 | AFR | LWK | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
homoSapiens_chm13v2 | hp1 | a0001 | c0002 | t0001 | g0050 | REF | REF | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
homoSapiens_grch38 | hp1 | a0001 | c0002 | t0001 | g0007 | REF | REF | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr20:43613966
|
A | G | 1 | a0002 | 1 | NA18906.hp1 | missense_variant | MODERATE | c.602A>G | p.Tyr201Cys | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 7/14 | 726/1754 | 602/1314 | 201/437 | chr20 | 43613966 | ||
chr20:43623897
|
G | C | 1 | a0006 | 1 | NA20129.hp1 | missense_variant | MODERATE | c.775G>C | p.Asp259His | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/14 | 899/1754 | 775/1314 | 259/437 | chr20 | 43623897 | ||
chr20:43623925
|
C | T | 1 | a0003 | 1 | HG02056.hp1 | missense_variant | MODERATE | c.803C>T | p.Thr268Ile | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/14 | 927/1754 | 803/1314 | 268/437 | chr20 | 43623925 | ||
chr20:43635933
|
G | A | 1 | a0005 | 1 | HG02083.hp2 | missense_variant | MODERATE | c.931G>A | p.Glu311Lys | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 11/14 | 1055/1754 | 931/1314 | 311/437 | chr20 | 43635933 | ||
chr20:43646955
|
G | A | 1 | a0004 | 1 | NA21309.hp1 | missense_variant | MODERATE | c.1286G>A | p.Ser429Asn | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 14/14 | 1410/1754 | 1286/1314 | 429/437 | chr20 | 43646955 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr20:43596474
|
G | A | 3 | a0001c0001a0004c0005a0006c0004 | 181 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(178): Show |
synonymous_variant | LOW | c.159G>A | p.Val53Val | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/14 | 283/1754 | 159/1314 | 53/437 | chr20 | 43596474 | ||
chr20:43613884
|
T | C | 1 | a0001c0006 | 1 | NA21309.hp2 | synonymous_variant | LOW | c.520T>C | p.Leu174Leu | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 7/14 | 644/1754 | 520/1314 | 174/437 | chr20 | 43613884 | ||
chr20:43623947
|
G | A | 1 | a0001c0003 | 6 | HG01361.hp2 HG02615.hp2 HG02922.hp2 others(3): Show |
synonymous_variant | LOW | c.825G>A | p.Glu275Glu | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/14 | 949/1754 | 825/1314 | 275/437 | chr20 | 43623947 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr20:43647036
|
A | G | 1 | a0004c0005t0003 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*53A>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 14/14 | 53 | chr20 | 43647036 | |||||
chr20:43647063
|
T | G | 1 | a0001c0001t0002 | 1 | NA19083.hp2 | 3_prime_UTR_variant | MODIFIER | c.*80T>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 14/14 | 80 | chr20 | 43647063 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr20:43591140
|
G | T | 179 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(176): Show | 186 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(183): Show |
intron_variant | MODIFIER | c.-7+86G>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 1/13 | chr20 | 43591140 | ||||||
chr20:43591191
|
G | A | 169 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(166): Show | 176 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(173): Show |
intron_variant | MODIFIER | c.-7+137G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 1/13 | chr20 | 43591191 | ||||||
chr20:43591351
|
A | G | 3 | a0001c0002t0001g0106a0001c0002t0001g0107a0001c0002t0001g0108 | 3 | HG02602.hp2 HG02615.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.-7+297A>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 1/13 | chr20 | 43591351 | ||||||
chr20:43591642
|
T | A | 1 | a0001c0001t0001g0109 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.-7+588T>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 1/13 | chr20 | 43591642 | ||||||
chr20:43591713
|
C | T | 25 | a0001c0002t0001g0009a0001c0002t0001g0010a0001c0002t0001g0083others(22): Show | 27 | HG01081.hp1 HG02083.hp2 HG02486.hp2 others(24): Show |
intron_variant | MODIFIER | c.-7+659C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 1/13 | chr20 | 43591713 | ||||||
chr20:43591718
|
A | G | 1 | a0001c0002t0001g0082 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-7+664A>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 1/13 | chr20 | 43591718 | ||||||
chr20:43591728
|
A | G | 179 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(176): Show | 186 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(183): Show |
intron_variant | MODIFIER | c.-7+674A>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 1/13 | chr20 | 43591728 | ||||||
chr20:43591792
|
A | G | 1 | a0001c0002t0001g0105 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-7+738A>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 1/13 | chr20 | 43591792 | ||||||
chr20:43591800
|
G | A | 4 | a0001c0002t0001g0083a0001c0002t0001g0084a0001c0002t0001g0085others(1): Show | 4 | HG02717.hp1 HG02886.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.-7+746G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 1/13 | chr20 | 43591800 | ||||||
chr20:43592040
|
A | G | 2 | a0001c0001t0001g0015a0001c0001t0001g0271 | 3 | HG01123.hp2 HG01346.hp2 HG01934.hp1 |
intron_variant | MODIFIER | c.-7+986A>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 1/13 | chr20 | 43592040 | ||||||
chr20:43592125
|
C | T | 1 | a0001c0001t0001g0270 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-7+1071C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 1/13 | chr20 | 43592125 | ||||||
chr20:43592129
|
T | A | 3 | a0001c0002t0001g0106a0001c0002t0001g0107a0001c0002t0001g0108 | 3 | HG02602.hp2 HG02615.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.-7+1075T>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 1/13 | chr20 | 43592129 | ||||||
chr20:43592570
|
C | CAA | 28 | a0001c0002t0001g0009a0001c0002t0001g0010a0001c0002t0001g0017others(25): Show | 30 | HG01081.hp1 HG01884.hp1 HG02083.hp2 others(27): Show |
intron_variant | MODIFIER | c.-7+1530_-7+1531dup others(2): Show |
IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr20 | 43592570 | |||||
chr20:43592570
|
CA | C | 159 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(156): Show | 166 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.-7+1531delA | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr20 | 43592570 | |||||
chr20:43592660
|
G | A | 218 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(215): Show | 230 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.-7+1606G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 1/13 | chr20 | 43592660 | ||||||
chr20:43592828
|
C | T | 1 | a0001c0002t0001g0269 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-7+1774C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 1/13 | chr20 | 43592828 | ||||||
chr20:43592922
|
G | A | 1 | a0001c0001t0001g0121 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.-6-1771G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 1/13 | chr20 | 43592922 | ||||||
chr20:43592963
|
C | T | 1 | a0001c0001t0001g0268 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.-6-1730C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 1/13 | chr20 | 43592963 | ||||||
chr20:43592966
|
G | A | 169 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(166): Show | 176 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(173): Show |
intron_variant | MODIFIER | c.-6-1727G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 1/13 | chr20 | 43592966 | ||||||
chr20:43592993
|
T | G | 179 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(176): Show | 186 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(183): Show |
intron_variant | MODIFIER | c.-6-1700T>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 1/13 | chr20 | 43592993 | ||||||
chr20:43593098
|
C | T | 14 | a0001c0002t0001g0010a0001c0002t0001g0092a0001c0002t0001g0093others(11): Show | 15 | HG02083.hp2 HG03491.hp2 HG03492.hp1 others(12): Show |
intron_variant | MODIFIER | c.-6-1595C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 1/13 | chr20 | 43593098 | ||||||
chr20:43593113
|
T | G | 22 | a0001c0002t0001g0009a0001c0002t0001g0010a0001c0002t0001g0087others(19): Show | 24 | HG01081.hp1 HG02083.hp2 HG02486.hp2 others(21): Show |
intron_variant | MODIFIER | c.-6-1580T>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 1/13 | chr20 | 43593113 | ||||||
chr20:43593116
|
G | T | 10 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0274others(7): Show | 10 | HG00741.hp2 HG01167.hp2 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.-6-1577G>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 1/13 | chr20 | 43593116 | ||||||
chr20:43593119
|
G | T | 1 | a0001c0001t0001g0281 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-6-1574G>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 1/13 | chr20 | 43593119 | ||||||
chr20:43593128
|
A | T | 1 | a0001c0002t0001g0010 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.-6-1565A>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 1/13 | chr20 | 43593128 | ||||||
chr20:43593200
|
A | G | 1 | a0001c0001t0001g0267 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.-6-1493A>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 1/13 | chr20 | 43593200 | ||||||
chr20:43593331
|
G | A | 1 | a0001c0006t0001g0016 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-6-1362G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 1/13 | chr20 | 43593331 | ||||||
chr20:43593555
|
G | A | 1 | a0001c0002t0001g0024 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-6-1138G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 1/13 | chr20 | 43593555 | ||||||
chr20:43593755
|
G | T | 179 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(176): Show | 186 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(183): Show |
intron_variant | MODIFIER | c.-6-938G>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 1/13 | chr20 | 43593755 | ||||||
chr20:43593801
|
C | T | 1 | a0001c0001t0001g0266 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-6-892C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 1/13 | chr20 | 43593801 | ||||||
chr20:43593812
|
C | T | 2 | a0001c0002t0001g0017a0001c0002t0001g0018 | 2 | HG01884.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.-6-881C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 1/13 | chr20 | 43593812 | ||||||
chr20:43593968
|
G | A | 17 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0024others(14): Show | 19 | HG01109.hp2 HG02056.hp1 HG02135.hp1 others(16): Show |
intron_variant | MODIFIER | c.-6-725G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 1/13 | chr20 | 43593968 | ||||||
chr20:43594026
|
C | T | 1 | a0001c0002t0001g0038 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.-6-667C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 1/13 | chr20 | 43594026 | ||||||
chr20:43594123
|
C | G | 1 | a0001c0002t0001g0080 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-6-570C>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 1/13 | chr20 | 43594123 | ||||||
chr20:43594141
|
C | T | 1 | a0001c0001t0001g0265 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-6-552C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 1/13 | chr20 | 43594141 | ||||||
chr20:43594344
|
T | C | 218 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(215): Show | 230 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.-6-349T>C | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 1/13 | chr20 | 43594344 | ||||||
chr20:43594347
|
G | A | 2 | a0001c0002t0001g0004a0001c0002t0001g0019 | 3 | HG02723.hp2 HG02976.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-6-346G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 1/13 | chr20 | 43594347 | ||||||
chr20:43594429
|
A | T | 1 | a0001c0001t0001g0264 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.-6-264A>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 1/13 | chr20 | 43594429 | ||||||
chr20:43594822
|
C | T | 4 | a0001c0002t0001g0083a0001c0002t0001g0084a0001c0002t0001g0085others(1): Show | 4 | HG02717.hp1 HG02886.hp1 HG02896.hp2 others(1): Show |
splice_region_variant&intron_variant | LOW | c.119+5C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 2/13 | chr20 | 43594822 | ||||||
chr20:43595049
|
C | G | 21 | a0001c0002t0001g0009a0001c0002t0001g0010a0001c0002t0001g0087others(18): Show | 23 | HG01081.hp1 HG02083.hp2 HG02486.hp2 others(20): Show |
intron_variant | MODIFIER | c.119+232C>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 2/13 | chr20 | 43595049 | ||||||
chr20:43595087
|
G | A | 4 | a0001c0002t0001g0083a0001c0002t0001g0084a0001c0002t0001g0085others(1): Show | 4 | HG02717.hp1 HG02886.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.119+270G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 2/13 | chr20 | 43595087 | ||||||
chr20:43595174
|
G | A | 3 | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0001t0001g0125 | 3 | HG02055.hp1 HG02809.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.119+357G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 2/13 | chr20 | 43595174 | ||||||
chr20:43595316
|
C | CAAAAA | 8 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0274others(5): Show | 8 | HG01167.hp2 HG01243.hp1 HG01261.hp1 others(5): Show |
intron_variant | MODIFIER | c.119+517_119+521dup others(5): Show |
IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr20 | 43595316 | |||||
chr20:43595316
|
CA | C | 153 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(150): Show | 160 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.119+521delA | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr20 | 43595316 | |||||
chr20:43595316
|
CAA | C | 14 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0252others(11): Show | 14 | HG01243.hp2 HG02040.hp1 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.119+520_119+521del others(2): Show |
IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr20 | 43595316 | |||||
chr20:43595335
|
A | G | 1 | a0001c0002t0001g0079 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.119+518A>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 2/13 | chr20 | 43595335 | ||||||
chr20:43595363
|
A | G | 21 | a0001c0002t0001g0009a0001c0002t0001g0010a0001c0002t0001g0087others(18): Show | 23 | HG01081.hp1 HG02083.hp2 HG02486.hp2 others(20): Show |
intron_variant | MODIFIER | c.119+546A>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 2/13 | chr20 | 43595363 | ||||||
chr20:43595370
|
G | A | 1 | a0001c0001t0001g0110 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.119+553G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 2/13 | chr20 | 43595370 | ||||||
chr20:43595415
|
C | T | 7 | a0001c0001t0001g0246a0001c0001t0001g0247a0001c0001t0001g0248others(4): Show | 7 | HG00738.hp2 HG02258.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.119+598C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 2/13 | chr20 | 43595415 | ||||||
chr20:43595463
|
C | T | 3 | a0001c0002t0001g0106a0001c0002t0001g0107a0001c0002t0001g0108 | 3 | HG02602.hp2 HG02615.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.119+646C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 2/13 | chr20 | 43595463 | ||||||
chr20:43595915
|
C | T | 1 | a0001c0001t0001g0245 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.120-520C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 2/13 | chr20 | 43595915 | ||||||
chr20:43596073
|
T | C | 1 | a0001c0001t0001g0129 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.120-362T>C | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 2/13 | chr20 | 43596073 | ||||||
chr20:43596189
|
T | C | 8 | a0001c0002t0001g0017a0001c0002t0001g0018a0001c0003t0001g0002others(5): Show | 10 | HG01361.hp2 HG01884.hp1 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.120-246T>C | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 2/13 | chr20 | 43596189 | ||||||
chr20:43596255
|
T | G | 3 | a0001c0002t0001g0106a0001c0002t0001g0107a0001c0002t0001g0108 | 3 | HG02602.hp2 HG02615.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.120-180T>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 2/13 | chr20 | 43596255 | ||||||
chr20:43596736
|
C | CT | 10 | a0001c0001t0001g0258a0001c0001t0001g0259a0001c0001t0001g0260others(7): Show | 11 | HG01243.hp2 HG01361.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.207+237dupT | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr20 | 43596736 | |||||
chr20:43596736
|
CT | C | 165 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(162): Show | 172 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(169): Show |
intron_variant | MODIFIER | c.207+237delT | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr20 | 43596736 | |||||
chr20:43596765
|
A | G | 3 | a0001c0001t0001g0235a0001c0001t0001g0236a0001c0001t0001g0237 | 3 | HG01167.hp1 HG01169.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.207+243A>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | chr20 | 43596765 | ||||||
chr20:43596772
|
C | T | 2 | a0001c0001t0001g0233a0001c0001t0001g0234 | 2 | HG01261.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.207+250C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | chr20 | 43596772 | ||||||
chr20:43596783
|
C | T | 3 | a0001c0002t0001g0106a0001c0002t0001g0107a0001c0002t0001g0108 | 3 | HG02602.hp2 HG02615.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.207+261C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | chr20 | 43596783 | ||||||
chr20:43596803
|
G | A | 4 | a0001c0002t0001g0083a0001c0002t0001g0084a0001c0002t0001g0085others(1): Show | 4 | HG02717.hp1 HG02886.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.207+281G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | chr20 | 43596803 | ||||||
chr20:43596806
|
A | G | 1 | a0001c0002t0001g0080 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.207+284A>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | chr20 | 43596806 | ||||||
chr20:43596834
|
C | G | 4 | a0001c0001t0001g0229a0001c0001t0001g0230a0001c0001t0001g0231others(1): Show | 4 | HG01884.hp2 HG02145.hp1 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.207+312C>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | chr20 | 43596834 | ||||||
chr20:43596834
|
C | T | 1 | a0001c0002t0001g0077 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.207+312C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | chr20 | 43596834 | ||||||
chr20:43597037
|
A | G | 180 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(177): Show | 187 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.207+515A>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | chr20 | 43597037 | ||||||
chr20:43597042
|
G | C | 220 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(217): Show | 232 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(229): Show |
intron_variant | MODIFIER | c.207+520G>C | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | chr20 | 43597042 | ||||||
chr20:43597128
|
T | C | 2 | a0001c0002t0001g0025a0001c0002t0001g0026 | 2 | NA18955.hp2 NA19089.hp2 |
intron_variant | MODIFIER | c.207+606T>C | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | chr20 | 43597128 | ||||||
chr20:43597198
|
C | G | 26 | a0001c0002t0001g0009a0001c0002t0001g0010a0001c0002t0001g0083others(23): Show | 28 | HG00735.hp2 HG01081.hp1 HG02083.hp2 others(25): Show |
intron_variant | MODIFIER | c.207+676C>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | chr20 | 43597198 | ||||||
chr20:43597283
|
A | G | 168 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(165): Show | 175 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.207+761A>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | chr20 | 43597283 | ||||||
chr20:43597303
|
G | A | 4 | a0001c0002t0001g0083a0001c0002t0001g0084a0001c0002t0001g0085others(1): Show | 4 | HG02717.hp1 HG02886.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.207+781G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | chr20 | 43597303 | ||||||
chr20:43597381
|
A | AAAAG | 260 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(257): Show | 275 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(272): Show |
intron_variant | MODIFIER | c.207+867_207+870dup others(4): Show |
IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr20 | 43597381 | |||||
chr20:43597460
|
G | A | 1 | a0001c0002t0001g0239 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.207+938G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | chr20 | 43597460 | ||||||
chr20:43597670
|
G | T | 1 | a0001c0002t0001g0104 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.207+1148G>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | chr20 | 43597670 | ||||||
chr20:43597767
|
G | A | 6 | a0001c0001t0001g0258a0001c0001t0001g0259a0001c0001t0001g0260others(3): Show | 6 | HG01243.hp2 HG02055.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.207+1245G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | chr20 | 43597767 | ||||||
chr20:43597847
|
C | T | 174 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(171): Show | 181 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(178): Show |
intron_variant | MODIFIER | c.207+1325C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | chr20 | 43597847 | ||||||
chr20:43597866
|
G | C | 177 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(174): Show | 184 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(181): Show |
intron_variant | MODIFIER | c.207+1344G>C | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | chr20 | 43597866 | ||||||
chr20:43597890
|
C | CA | 172 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(169): Show | 181 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(178): Show |
intron_variant | MODIFIER | c.207+1389dupA | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr20 | 43597890 | |||||
chr20:43597890
|
C | CAA | 31 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0113others(28): Show | 33 | HG00735.hp1 HG00738.hp1 HG01106.hp1 others(30): Show |
intron_variant | MODIFIER | c.207+1388_207+1389d others(4): Show |
IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr20 | 43597890 | |||||
chr20:43598145
|
A | T | 3 | a0001c0002t0001g0106a0001c0002t0001g0107a0001c0002t0001g0108 | 3 | HG02602.hp2 HG02615.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.207+1623A>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | chr20 | 43598145 | ||||||
chr20:43598150
|
T | C | 26 | a0001c0002t0001g0009a0001c0002t0001g0010a0001c0002t0001g0087others(23): Show | 28 | HG00735.hp2 HG01081.hp1 HG02083.hp2 others(25): Show |
intron_variant | MODIFIER | c.207+1628T>C | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | chr20 | 43598150 | ||||||
chr20:43598365
|
G | A | 1 | a0001c0001t0001g0131 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.207+1843G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | chr20 | 43598365 | ||||||
chr20:43598372
|
G | A | 155 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(152): Show | 162 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(159): Show |
intron_variant | MODIFIER | c.207+1850G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | chr20 | 43598372 | ||||||
chr20:43598423
|
G | A | 2 | a0001c0002t0001g0027a0001c0002t0001g0082 | 2 | HG02135.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.207+1901G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | chr20 | 43598423 | ||||||
chr20:43598609
|
C | T | 1 | a0002c0009t0001g0020 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.207+2087C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | chr20 | 43598609 | ||||||
chr20:43598657
|
C | T | 1 | a0001c0006t0001g0016 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.207+2135C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | chr20 | 43598657 | ||||||
chr20:43598706
|
A | T | 1 | a0001c0001t0001g0120 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.207+2184A>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | chr20 | 43598706 | ||||||
chr20:43598871
|
A | G | 174 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(171): Show | 181 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(178): Show |
intron_variant | MODIFIER | c.207+2349A>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | chr20 | 43598871 | ||||||
chr20:43599031
|
G | C | 1 | a0001c0002t0001g0019 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.207+2509G>C | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | chr20 | 43599031 | ||||||
chr20:43599314
|
C | T | 3 | a0001c0001t0001g0117a0001c0001t0001g0119a0001c0001t0001g0120 | 3 | HG02486.hp1 HG02886.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.207+2792C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | chr20 | 43599314 | ||||||
chr20:43599545
|
CT | C | 10 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0274others(7): Show | 10 | HG00741.hp2 HG01167.hp2 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.207+3030delT | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr20 | 43599545 | |||||
chr20:43599673
|
G | A | 2 | a0001c0002t0001g0040a0001c0002t0001g0041 | 2 | HG02258.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.207+3151G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | chr20 | 43599673 | ||||||
chr20:43599898
|
A | G | 1 | a0001c0001t0001g0228 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.207+3376A>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | chr20 | 43599898 | ||||||
chr20:43600235
|
A | G | 22 | a0001c0001t0001g0225a0001c0002t0001g0009a0001c0002t0001g0010others(19): Show | 24 | HG01081.hp1 HG02083.hp2 HG02486.hp2 others(21): Show |
intron_variant | MODIFIER | c.208-3525A>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | chr20 | 43600235 | ||||||
chr20:43600304
|
A | AT | 18 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0267others(15): Show | 19 | HG01433.hp2 HG02083.hp2 HG02148.hp2 others(16): Show |
intron_variant | MODIFIER | c.208-3441dupT | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr20 | 43600304 | |||||
chr20:43600344
|
A | G | 180 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(177): Show | 187 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.208-3416A>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | chr20 | 43600344 | ||||||
chr20:43600397
|
C | T | 2 | a0001c0002t0001g0092a0001c0002t0001g0103 | 2 | NA18971.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.208-3363C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | chr20 | 43600397 | ||||||
chr20:43600465
|
C | T | 1 | a0001c0001t0001g0256 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.208-3295C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | chr20 | 43600465 | ||||||
chr20:43600518
|
G | A | 3 | a0001c0001t0001g0142a0001c0001t0001g0143a0001c0002t0001g0028 | 3 | HG01069.hp1 HG01071.hp2 HG01109.hp2 |
intron_variant | MODIFIER | c.208-3242G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | chr20 | 43600518 | ||||||
chr20:43600521
|
A | G | 3 | a0001c0001t0001g0142a0001c0001t0001g0143a0001c0002t0001g0028 | 3 | HG01069.hp1 HG01071.hp2 HG01109.hp2 |
intron_variant | MODIFIER | c.208-3239A>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | chr20 | 43600521 | ||||||
chr20:43600549
|
CCGCCTTG others(9): Show |
C | 1 | a0001c0002t0001g0026 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.208-3210_208-3195d others(18): Show |
IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | chr20 | 43600549 | ||||||
chr20:43600551
|
G | A | 16 | a0001c0001t0001g0117a0001c0001t0001g0119a0001c0001t0001g0120others(13): Show | 16 | HG00741.hp2 HG01167.hp2 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.208-3209G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | chr20 | 43600551 | ||||||
chr20:43600569
|
G | A | 1 | a0001c0002t0001g0026 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.208-3191G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | chr20 | 43600569 | ||||||
chr20:43600570
|
T | A | 1 | a0001c0002t0001g0026 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.208-3190T>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | chr20 | 43600570 | ||||||
chr20:43600571
|
T | A | 1 | a0001c0002t0001g0026 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.208-3189T>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | chr20 | 43600571 | ||||||
chr20:43600572
|
C | A | 1 | a0001c0002t0001g0026 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.208-3188C>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | chr20 | 43600572 | ||||||
chr20:43600573
|
T | A | 1 | a0001c0002t0001g0026 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.208-3187T>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | chr20 | 43600573 | ||||||
chr20:43600575
|
T | A | 1 | a0001c0002t0001g0026 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.208-3185T>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | chr20 | 43600575 | ||||||
chr20:43600576
|
T | A | 1 | a0001c0002t0001g0026 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.208-3184T>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | chr20 | 43600576 | ||||||
chr20:43600579
|
T | A | 1 | a0001c0002t0001g0026 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.208-3181T>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | chr20 | 43600579 | ||||||
chr20:43600585
|
G | A | 1 | a0001c0002t0001g0026 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.208-3175G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | chr20 | 43600585 | ||||||
chr20:43600587
|
G | A | 1 | a0001c0002t0001g0026 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.208-3173G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | chr20 | 43600587 | ||||||
chr20:43600588
|
T | TAAAAAAA others(22): Show |
1 | a0001c0002t0001g0026 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.208-3171_208-3170i others(31): Show |
IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr20 | 43600588 | |||||
chr20:43600598
|
C | A | 1 | a0001c0002t0001g0026 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.208-3162C>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | chr20 | 43600598 | ||||||
chr20:43600600
|
C | A | 1 | a0001c0002t0001g0026 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.208-3160C>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | chr20 | 43600600 | ||||||
chr20:43600601
|
T | A | 1 | a0001c0002t0001g0026 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.208-3159T>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | chr20 | 43600601 | ||||||
chr20:43600602
|
C | A | 1 | a0001c0002t0001g0026 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.208-3158C>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | chr20 | 43600602 | ||||||
chr20:43600607
|
T | A | 1 | a0001c0002t0001g0026 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.208-3153T>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | chr20 | 43600607 | ||||||
chr20:43600609
|
C | A | 1 | a0001c0002t0001g0026 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.208-3151C>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | chr20 | 43600609 | ||||||
chr20:43600610
|
A | G | 1 | a0001c0001t0001g0224 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.208-3150A>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | chr20 | 43600610 | ||||||
chr20:43600612
|
G | C | 1 | a0001c0002t0001g0026 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.208-3148G>C | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | chr20 | 43600612 | ||||||
chr20:43600724
|
A | T | 1 | a0001c0002t0001g0026 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.208-3036A>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | chr20 | 43600724 | ||||||
chr20:43600762
|
G | A | 1 | a0001c0001t0001g0133 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.208-2998G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | chr20 | 43600762 | ||||||
chr20:43600830
|
G | A | 178 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(175): Show | 185 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.208-2930G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | chr20 | 43600830 | ||||||
chr20:43600860
|
A | G | 1 | a0001c0001t0001g0221 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.208-2900A>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | chr20 | 43600860 | ||||||
chr20:43601206
|
T | C | 9 | a0001c0002t0001g0017a0001c0002t0001g0018a0001c0002t0001g0082others(6): Show | 11 | HG01361.hp2 HG01884.hp1 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.208-2554T>C | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | chr20 | 43601206 | ||||||
chr20:43601280
|
A | C | 3 | a0001c0002t0001g0106a0001c0002t0001g0107a0001c0002t0001g0108 | 3 | HG02602.hp2 HG02615.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.208-2480A>C | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | chr20 | 43601280 | ||||||
chr20:43601419
|
A | G | 1 | a0003c0008t0001g0034 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.208-2341A>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | chr20 | 43601419 | ||||||
chr20:43601524
|
C | T | 1 | a0001c0002t0001g0076 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.208-2236C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | chr20 | 43601524 | ||||||
chr20:43601681
|
C | A | 2 | a0001c0002t0001g0017a0001c0002t0001g0018 | 2 | HG01884.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.208-2079C>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | chr20 | 43601681 | ||||||
chr20:43601754
|
A | G | 21 | a0001c0002t0001g0009a0001c0002t0001g0010a0001c0002t0001g0087others(18): Show | 23 | HG01081.hp1 HG02083.hp2 HG02486.hp2 others(20): Show |
intron_variant | MODIFIER | c.208-2006A>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | chr20 | 43601754 | ||||||
chr20:43601906
|
A | G | 1 | a0001c0002t0001g0238 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.208-1854A>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | chr20 | 43601906 | ||||||
chr20:43601917
|
A | G | 17 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0024others(14): Show | 19 | HG01109.hp2 HG02056.hp1 HG02135.hp1 others(16): Show |
intron_variant | MODIFIER | c.208-1843A>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | chr20 | 43601917 | ||||||
chr20:43601932
|
C | T | 1 | a0001c0002t0001g0076 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.208-1828C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | chr20 | 43601932 | ||||||
chr20:43601979
|
C | T | 1 | a0001c0002t0001g0082 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.208-1781C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | chr20 | 43601979 | ||||||
chr20:43601999
|
G | A | 11 | a0001c0001t0001g0003a0001c0001t0001g0131a0001c0001t0001g0134others(8): Show | 13 | HG00642.hp2 HG00733.hp1 HG00741.hp1 others(10): Show |
intron_variant | MODIFIER | c.208-1761G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | chr20 | 43601999 | ||||||
chr20:43602004
|
C | T | 218 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(215): Show | 230 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.208-1756C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | chr20 | 43602004 | ||||||
chr20:43602055
|
T | C | 159 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(156): Show | 166 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.208-1705T>C | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | chr20 | 43602055 | ||||||
chr20:43602113
|
C | T | 2 | a0001c0002t0001g0004a0001c0002t0001g0019 | 3 | HG02723.hp2 HG02976.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.208-1647C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | chr20 | 43602113 | ||||||
chr20:43602136
|
A | AT | 4 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0279others(1): Show | 4 | HG00741.hp2 HG01243.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.208-1619dupT | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr20 | 43602136 | |||||
chr20:43602136
|
ATTTTTAT others(9): Show |
A | 1 | a0004c0005t0003g0155 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.208-1621_208-1606d others(18): Show |
IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr20 | 43602136 | |||||
chr20:43602137
|
T | TTTTA | 19 | a0001c0002t0001g0009a0001c0002t0001g0010a0001c0002t0001g0088others(16): Show | 21 | HG01081.hp1 HG02083.hp2 HG02486.hp2 others(18): Show |
intron_variant | MODIFIER | c.208-1620_208-1619i others(6): Show |
IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr20 | 43602137 | |||||
chr20:43602138
|
T | TA | 3 | a0001c0001t0001g0152a0001c0001t0001g0241a0001c0001t0001g0265 | 3 | HG02622.hp1 HG02818.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.208-1622_208-1621i others(3): Show |
IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | chr20 | 43602138 | ||||||
chr20:43602138
|
T | TTA | 7 | a0001c0001t0001g0144a0001c0001t0001g0159a0001c0001t0001g0160others(4): Show | 7 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(4): Show |
intron_variant | MODIFIER | c.208-1621_208-1620i others(4): Show |
IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr20 | 43602138 | |||||
chr20:43602138
|
T | TTATTTA | 3 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0158 | 3 | HG01106.hp2 HG02145.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.208-1621_208-1620i others(8): Show |
IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr20 | 43602138 | |||||
chr20:43602138
|
T | TTTTTA | 34 | a0001c0001t0001g0011a0001c0001t0001g0109a0001c0001t0001g0117others(31): Show | 35 | HG00099.hp1 HG00597.hp1 HG00597.hp2 others(32): Show |
intron_variant | MODIFIER | c.208-1619_208-1618i others(7): Show |
IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr20 | 43602138 | |||||
chr20:43602138
|
T | TTTTTATT others(2): Show |
15 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0135others(12): Show | 15 | HG01243.hp2 HG02055.hp2 HG02071.hp1 others(12): Show |
intron_variant | MODIFIER | c.208-1619_208-1618i others(11): Show |
IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr20 | 43602138 | |||||
chr20:43602138
|
T | TTTTTATT others(6): Show |
1 | a0001c0002t0001g0239 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.208-1619_208-1618i others(15): Show |
IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr20 | 43602138 | |||||
chr20:43602139
|
T | A | 9 | a0001c0001t0001g0153a0001c0001t0001g0154a0001c0001t0001g0246others(6): Show | 9 | HG00738.hp2 HG01891.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.208-1621T>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | chr20 | 43602139 | ||||||
chr20:43602142
|
A | T | 110 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0013others(107): Show | 116 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.208-1618A>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | chr20 | 43602142 | ||||||
chr20:43602143
|
T | A | 18 | a0001c0001t0001g0153a0001c0001t0001g0154a0001c0001t0001g0183others(15): Show | 18 | HG00099.hp2 HG00738.hp2 HG01167.hp2 others(15): Show |
intron_variant | MODIFIER | c.208-1617T>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | chr20 | 43602143 | ||||||
chr20:43602143
|
T | TA | 10 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0132others(7): Show | 10 | HG01168.hp1 HG01169.hp1 HG01192.hp1 others(7): Show |
intron_variant | MODIFIER | c.208-1617_208-1616i others(3): Show |
IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | chr20 | 43602143 | ||||||
chr20:43602143
|
T | TATTTA | 16 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0123others(13): Show | 19 | HG00642.hp2 HG00741.hp1 HG01070.hp2 others(16): Show |
intron_variant | MODIFIER | c.208-1617_208-1616i others(7): Show |
IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | chr20 | 43602143 | ||||||
chr20:43602143
|
T | TATTTATT others(2): Show |
55 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0114others(52): Show | 57 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(54): Show |
intron_variant | MODIFIER | c.208-1617_208-1616i others(11): Show |
IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | chr20 | 43602143 | ||||||
chr20:43602143
|
T | TATTTATT others(6): Show |
11 | a0001c0001t0001g0015a0001c0001t0001g0110a0001c0001t0001g0111others(8): Show | 12 | HG00733.hp1 HG00738.hp1 HG01099.hp2 others(9): Show |
intron_variant | MODIFIER | c.208-1617_208-1616i others(15): Show |
IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | chr20 | 43602143 | ||||||
chr20:43602143
|
T | TTTA | 89 | a0001c0001t0001g0011a0001c0001t0001g0109a0001c0001t0001g0117others(86): Show | 92 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(89): Show |
intron_variant | MODIFIER | c.208-1615_208-1614i others(5): Show |
IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr20 | 43602143 | |||||
chr20:43602143
|
T | TTTTA | 32 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0024others(29): Show | 36 | HG01099.hp1 HG01361.hp2 HG01496.hp1 others(33): Show |
intron_variant | MODIFIER | c.208-1581_208-1578d others(6): Show |
IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr20 | 43602143 | |||||
chr20:43602143
|
T | TTTTATTT others(1): Show |
7 | a0001c0002t0001g0019a0001c0002t0001g0028a0001c0002t0001g0029others(4): Show | 7 | HG01109.hp2 HG02886.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.208-1585_208-1578d others(10): Show |
IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr20 | 43602143 | |||||
chr20:43602143
|
T | TTTTATTT others(5): Show |
2 | a0001c0002t0001g0018a0001c0006t0001g0016 | 2 | HG02630.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.208-1589_208-1578d others(14): Show |
IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr20 | 43602143 | |||||
chr20:43602143
|
T | TTTTATTT others(9): Show |
1 | a0001c0002t0001g0017 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.208-1593_208-1578d others(18): Show |
IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr20 | 43602143 | |||||
chr20:43602417
|
C | T | 1 | a0001c0002t0001g0082 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.208-1343C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | chr20 | 43602417 | ||||||
chr20:43602449
|
A | G | 1 | a0001c0001t0001g0228 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.208-1311A>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | chr20 | 43602449 | ||||||
chr20:43602542
|
T | C | 1 | a0001c0002t0001g0004 | 2 | HG02723.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.208-1218T>C | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | chr20 | 43602542 | ||||||
chr20:43602545
|
G | A | 1 | a0001c0001t0001g0218 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.208-1215G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | chr20 | 43602545 | ||||||
chr20:43602573
|
A | G | 1 | a0001c0002t0001g0102 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.208-1187A>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | chr20 | 43602573 | ||||||
chr20:43602854
|
T | G | 1 | a0001c0002t0001g0019 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.208-906T>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | chr20 | 43602854 | ||||||
chr20:43602968
|
C | A | 1 | a0004c0005t0003g0155 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.208-792C>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | chr20 | 43602968 | ||||||
chr20:43603074
|
T | G | 1 | a0001c0001t0001g0264 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.208-686T>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | chr20 | 43603074 | ||||||
chr20:43603082
|
A | G | 1 | a0001c0001t0001g0214 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.208-678A>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | chr20 | 43603082 | ||||||
chr20:43603151
|
C | G | 4 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0033others(1): Show | 6 | NA18946.hp1 NA18963.hp1 NA18984.hp1 others(3): Show |
intron_variant | MODIFIER | c.208-609C>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | chr20 | 43603151 | ||||||
chr20:43603170
|
C | T | 1 | a0001c0002t0001g0082 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.208-590C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | chr20 | 43603170 | ||||||
chr20:43603192
|
G | T | 39 | a0001c0002t0001g0004a0001c0002t0001g0009a0001c0002t0001g0010others(36): Show | 44 | HG01081.hp1 HG01361.hp2 HG01884.hp1 others(41): Show |
intron_variant | MODIFIER | c.208-568G>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | chr20 | 43603192 | ||||||
chr20:43603218
|
GC | G | 3 | a0001c0001t0001g0117a0001c0001t0001g0119a0001c0001t0001g0120 | 3 | HG02486.hp1 HG02886.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.208-541delC | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | chr20 | 43603218 | ||||||
chr20:43603230
|
A | G | 1 | a0001c0003t0001g0023 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.208-530A>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | chr20 | 43603230 | ||||||
chr20:43603548
|
T | C | 3 | a0001c0002t0001g0106a0001c0002t0001g0107a0001c0002t0001g0108 | 3 | HG02602.hp2 HG02615.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.208-212T>C | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | chr20 | 43603548 | ||||||
chr20:43603602
|
A | T | 6 | a0001c0002t0001g0093a0001c0002t0001g0097a0001c0002t0001g0098others(3): Show | 6 | NA18952.hp1 NA18972.hp1 NA19000.hp2 others(3): Show |
intron_variant | MODIFIER | c.208-158A>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | chr20 | 43603602 | ||||||
chr20:43603943
|
A | G | 1 | a0001c0002t0001g0004 | 2 | HG02723.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.337+54A>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 4/13 | chr20 | 43603943 | ||||||
chr20:43603947
|
C | A | 10 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0274others(7): Show | 10 | HG00741.hp2 HG01167.hp2 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.337+58C>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 4/13 | chr20 | 43603947 | ||||||
chr20:43603974
|
T | C | 1 | a0001c0001t0001g0129 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.337+85T>C | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 4/13 | chr20 | 43603974 | ||||||
chr20:43604014
|
C | G | 1 | a0001c0001t0001g0014 | 2 | HG03239.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.337+125C>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 4/13 | chr20 | 43604014 | ||||||
chr20:43604068
|
C | T | 1 | a0002c0009t0001g0020 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.338-115C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 4/13 | chr20 | 43604068 | ||||||
chr20:43604099
|
C | T | 2 | a0001c0001t0001g0233a0001c0001t0001g0234 | 2 | HG01261.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.338-84C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 4/13 | chr20 | 43604099 | ||||||
chr20:43604501
|
G | A | 1 | a0001c0002t0001g0019 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.413+243G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 5/13 | chr20 | 43604501 | ||||||
chr20:43604555
|
G | T | 1 | a0001c0001t0001g0213 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.413+297G>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 5/13 | chr20 | 43604555 | ||||||
chr20:43604642
|
G | A | 1 | a0002c0009t0001g0020 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.414-360G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 5/13 | chr20 | 43604642 | ||||||
chr20:43605185
|
G | A | 1 | a0001c0001t0001g0185 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.485+112G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | chr20 | 43605185 | ||||||
chr20:43605439
|
C | T | 1 | a0001c0002t0001g0122 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.485+366C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | chr20 | 43605439 | ||||||
chr20:43605472
|
C | T | 2 | a0001c0002t0001g0004a0001c0002t0001g0019 | 3 | HG02723.hp2 HG02976.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.485+399C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | chr20 | 43605472 | ||||||
chr20:43605473
|
G | A | 1 | a0001c0001t0001g0258 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.485+400G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | chr20 | 43605473 | ||||||
chr20:43605503
|
C | T | 10 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0274others(7): Show | 10 | HG00741.hp2 HG01167.hp2 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.485+430C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | chr20 | 43605503 | ||||||
chr20:43605582
|
T | G | 1 | a0001c0001t0001g0119 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.485+509T>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | chr20 | 43605582 | ||||||
chr20:43605618
|
C | T | 3 | a0001c0001t0001g0217a0001c0001t0001g0233a0001c0001t0001g0234 | 3 | HG01123.hp1 HG01261.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.485+545C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | chr20 | 43605618 | ||||||
chr20:43605806
|
T | G | 1 | a0006c0004t0001g0186 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.485+733T>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | chr20 | 43605806 | ||||||
chr20:43605810
|
A | G | 1 | a0006c0004t0001g0186 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.485+737A>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | chr20 | 43605810 | ||||||
chr20:43605811
|
T | A | 1 | a0006c0004t0001g0186 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.485+738T>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | chr20 | 43605811 | ||||||
chr20:43605813
|
C | A | 1 | a0006c0004t0001g0186 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.485+740C>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | chr20 | 43605813 | ||||||
chr20:43605819
|
T | G | 1 | a0006c0004t0001g0186 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.485+746T>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | chr20 | 43605819 | ||||||
chr20:43605820
|
G | A | 1 | a0006c0004t0001g0186 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.485+747G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | chr20 | 43605820 | ||||||
chr20:43605821
|
T | G | 1 | a0006c0004t0001g0186 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.485+748T>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | chr20 | 43605821 | ||||||
chr20:43605825
|
T | C | 1 | a0006c0004t0001g0186 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.485+752T>C | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | chr20 | 43605825 | ||||||
chr20:43605826
|
G | T | 1 | a0006c0004t0001g0186 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.485+753G>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | chr20 | 43605826 | ||||||
chr20:43605828
|
C | T | 1 | a0006c0004t0001g0186 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.485+755C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | chr20 | 43605828 | ||||||
chr20:43605830
|
A | T | 1 | a0006c0004t0001g0186 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.485+757A>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | chr20 | 43605830 | ||||||
chr20:43605831
|
A | C | 1 | a0006c0004t0001g0186 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.485+758A>C | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | chr20 | 43605831 | ||||||
chr20:43605832
|
A | T | 1 | a0006c0004t0001g0186 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.485+759A>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | chr20 | 43605832 | ||||||
chr20:43605834
|
G | T | 1 | a0006c0004t0001g0186 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.485+761G>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | chr20 | 43605834 | ||||||
chr20:43605835
|
C | T | 1 | a0006c0004t0001g0186 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.485+762C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | chr20 | 43605835 | ||||||
chr20:43605836
|
A | C | 1 | a0006c0004t0001g0186 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.485+763A>C | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | chr20 | 43605836 | ||||||
chr20:43605840
|
G | T | 1 | a0006c0004t0001g0186 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.485+767G>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | chr20 | 43605840 | ||||||
chr20:43605841
|
A | C | 1 | a0006c0004t0001g0186 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.485+768A>C | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | chr20 | 43605841 | ||||||
chr20:43605844
|
A | C | 1 | a0006c0004t0001g0186 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.485+771A>C | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | chr20 | 43605844 | ||||||
chr20:43605848
|
T | C | 1 | a0006c0004t0001g0186 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.485+775T>C | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | chr20 | 43605848 | ||||||
chr20:43605849
|
G | GTTGTTGT others(3): Show |
1 | a0006c0004t0001g0186 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.485+777_485+778ins others(10): Show |
IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr20 | 43605849 | |||||
chr20:43605852
|
T | A | 1 | a0006c0004t0001g0186 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.485+779T>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | chr20 | 43605852 | ||||||
chr20:43605853
|
C | G | 1 | a0006c0004t0001g0186 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.485+780C>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | chr20 | 43605853 | ||||||
chr20:43605857
|
A | G | 1 | a0006c0004t0001g0186 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.485+784A>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | chr20 | 43605857 | ||||||
chr20:43605858
|
C | A | 1 | a0006c0004t0001g0186 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.485+785C>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | chr20 | 43605858 | ||||||
chr20:43605863
|
A | T | 2 | a0001c0001t0001g0140a0001c0001t0001g0212 | 2 | HG03654.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.485+790A>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | chr20 | 43605863 | ||||||
chr20:43606012
|
C | T | 4 | a0001c0002t0001g0083a0001c0002t0001g0084a0001c0002t0001g0085others(1): Show | 4 | HG02717.hp1 HG02886.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.485+939C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | chr20 | 43606012 | ||||||
chr20:43606215
|
C | T | 1 | a0001c0001t0001g0273 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.485+1142C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | chr20 | 43606215 | ||||||
chr20:43606216
|
G | C | 1 | a0001c0006t0001g0016 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.485+1143G>C | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | chr20 | 43606216 | ||||||
chr20:43606273
|
C | CT | 34 | a0001c0001t0001g0133a0001c0001t0001g0210a0001c0001t0001g0211others(31): Show | 36 | HG01109.hp2 HG01175.hp1 HG01433.hp1 others(33): Show |
intron_variant | MODIFIER | c.485+1218dupT | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr20 | 43606273 | |||||
chr20:43606296
|
T | C | 218 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(215): Show | 230 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.485+1223T>C | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | chr20 | 43606296 | ||||||
chr20:43606507
|
C | T | 2 | a0001c0002t0001g0106a0001c0002t0001g0108 | 2 | HG02602.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.485+1434C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | chr20 | 43606507 | ||||||
chr20:43606591
|
A | AT | 11 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0274others(8): Show | 11 | HG00741.hp2 HG01167.hp2 HG01243.hp1 others(8): Show |
intron_variant | MODIFIER | c.485+1531dupT | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr20 | 43606591 | |||||
chr20:43606956
|
AAAATGAA others(33): Show |
A | 1 | a0001c0001t0001g0271 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.485+1885_485+1924d others(42): Show |
IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr20 | 43606956 | |||||
chr20:43607059
|
C | T | 1 | a0001c0001t0001g0113 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.485+1986C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | chr20 | 43607059 | ||||||
chr20:43607078
|
C | T | 27 | a0001c0002t0001g0009a0001c0002t0001g0010a0001c0002t0001g0017others(24): Show | 29 | HG01081.hp1 HG01884.hp1 HG02083.hp2 others(26): Show |
intron_variant | MODIFIER | c.485+2005C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | chr20 | 43607078 | ||||||
chr20:43607159
|
G | T | 1 | a0002c0009t0001g0020 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.485+2086G>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | chr20 | 43607159 | ||||||
chr20:43607171
|
C | T | 1 | a0001c0002t0001g0082 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.485+2098C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | chr20 | 43607171 | ||||||
chr20:43607185
|
T | TGGACGGG others(42): Show |
1 | a0006c0004t0001g0186 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.485+2115_485+2116i others(51): Show |
IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr20 | 43607185 | |||||
chr20:43607185
|
TGGATGGG others(42): Show |
T | 3 | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0001t0001g0125 | 3 | HG02055.hp1 HG02809.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.485+2116_485+2164d others(51): Show |
IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr20 | 43607185 | |||||
chr20:43607189
|
T | C | 176 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(173): Show | 183 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(180): Show |
intron_variant | MODIFIER | c.485+2116T>C | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | chr20 | 43607189 | ||||||
chr20:43607189
|
T | G | 1 | a0001c0001t0001g0139 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.485+2116T>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | chr20 | 43607189 | ||||||
chr20:43607189
|
TGGGGCGG others(42): Show |
T | 24 | a0001c0002t0001g0004a0001c0002t0001g0009a0001c0002t0001g0010others(21): Show | 27 | HG01081.hp1 HG02083.hp2 HG02486.hp2 others(24): Show |
intron_variant | MODIFIER | c.485+2179_485+2227d others(51): Show |
IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr20 | 43607189 | |||||
chr20:43607255
|
C | T | 4 | a0001c0002t0001g0083a0001c0002t0001g0084a0001c0002t0001g0085others(1): Show | 4 | HG02717.hp1 HG02886.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.485+2182C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | chr20 | 43607255 | ||||||
chr20:43607260
|
G | A | 1 | a0001c0001t0001g0213 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.485+2187G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | chr20 | 43607260 | ||||||
chr20:43607378
|
TGGCTGCC others(33): Show |
T | 1 | a0001c0001t0001g0265 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.485+2341_485+2380d others(42): Show |
IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr20 | 43607378 | |||||
chr20:43607419
|
G | A | 27 | a0001c0002t0001g0009a0001c0002t0001g0010a0001c0002t0001g0017others(24): Show | 29 | HG01081.hp1 HG01884.hp1 HG02083.hp2 others(26): Show |
intron_variant | MODIFIER | c.485+2346G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | chr20 | 43607419 | ||||||
chr20:43607429
|
C | T | 8 | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0001t0001g0125others(5): Show | 8 | HG01891.hp2 HG02055.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.485+2356C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | chr20 | 43607429 | ||||||
chr20:43607491
|
G | A | 1 | a0001c0002t0001g0269 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.485+2418G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | chr20 | 43607491 | ||||||
chr20:43607695
|
C | G | 3 | a0001c0002t0001g0106a0001c0002t0001g0107a0001c0002t0001g0108 | 3 | HG02602.hp2 HG02615.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.485+2622C>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | chr20 | 43607695 | ||||||
chr20:43607739
|
C | CG | 4 | a0001c0002t0001g0030a0001c0002t0001g0052a0001c0002t0001g0064others(1): Show | 4 | HG01175.hp1 HG02056.hp2 NA18950.hp2 others(1): Show |
intron_variant | MODIFIER | c.485+2670dupG | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr20 | 43607739 | |||||
chr20:43607814
|
G | A | 180 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(177): Show | 187 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.485+2741G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | chr20 | 43607814 | ||||||
chr20:43607928
|
C | T | 21 | a0001c0002t0001g0009a0001c0002t0001g0010a0001c0002t0001g0087others(18): Show | 23 | HG01081.hp1 HG02083.hp2 HG02486.hp2 others(20): Show |
intron_variant | MODIFIER | c.485+2855C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | chr20 | 43607928 | ||||||
chr20:43607938
|
A | T | 1 | a0001c0002t0001g0101 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.485+2865A>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | chr20 | 43607938 | ||||||
chr20:43608021
|
G | A | 2 | a0001c0001t0001g0169a0001c0001t0001g0242 | 2 | HG02683.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.485+2948G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | chr20 | 43608021 | ||||||
chr20:43608031
|
A | G | 180 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(177): Show | 187 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.485+2958A>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | chr20 | 43608031 | ||||||
chr20:43608039
|
T | C | 1 | a0001c0001t0001g0146 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.485+2966T>C | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | chr20 | 43608039 | ||||||
chr20:43608057
|
A | AG | 180 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(177): Show | 187 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.485+2984_485+2985i others(3): Show |
IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | chr20 | 43608057 | ||||||
chr20:43608161
|
GGGGAGAG others(5): Show |
G | 1 | a0001c0001t0001g0221 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.485+3106_485+3117d others(14): Show |
IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr20 | 43608161 | |||||
chr20:43608403
|
T | A | 5 | a0001c0001t0001g0156a0001c0001t0001g0159a0001c0001t0001g0160others(2): Show | 5 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(2): Show |
intron_variant | MODIFIER | c.485+3330T>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | chr20 | 43608403 | ||||||
chr20:43608404
|
A | T | 1 | a0001c0001t0001g0253 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.485+3331A>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | chr20 | 43608404 | ||||||
chr20:43608427
|
C | A | 180 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(177): Show | 187 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.485+3354C>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | chr20 | 43608427 | ||||||
chr20:43608765
|
G | A | 10 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0274others(7): Show | 10 | HG00741.hp2 HG01167.hp2 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.485+3692G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | chr20 | 43608765 | ||||||
chr20:43608862
|
T | C | 235 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(232): Show | 249 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(246): Show |
intron_variant | MODIFIER | c.485+3789T>C | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | chr20 | 43608862 | ||||||
chr20:43608863
|
G | A | 21 | a0001c0002t0001g0009a0001c0002t0001g0010a0001c0002t0001g0087others(18): Show | 23 | HG01081.hp1 HG02083.hp2 HG02486.hp2 others(20): Show |
intron_variant | MODIFIER | c.485+3790G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | chr20 | 43608863 | ||||||
chr20:43609208
|
C | T | 1 | a0001c0002t0001g0082 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.485+4135C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | chr20 | 43609208 | ||||||
chr20:43609284
|
A | G | 1 | a0001c0002t0001g0051 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.485+4211A>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | chr20 | 43609284 | ||||||
chr20:43609547
|
G | A | 6 | a0001c0002t0001g0017a0001c0002t0001g0018a0001c0002t0001g0083others(3): Show | 6 | HG01884.hp1 HG02630.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.486-4303G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | chr20 | 43609547 | ||||||
chr20:43609610
|
A | T | 170 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(167): Show | 177 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(174): Show |
intron_variant | MODIFIER | c.486-4240A>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | chr20 | 43609610 | ||||||
chr20:43609775
|
C | CA | 8 | a0001c0001t0001g0144a0001c0001t0001g0219a0001c0002t0001g0028others(5): Show | 8 | HG01074.hp1 HG01109.hp2 HG01952.hp2 others(5): Show |
intron_variant | MODIFIER | c.486-4051dupA | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr20 | 43609775 | |||||
chr20:43609775
|
CA | C | 182 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(179): Show | 191 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.486-4051delA | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr20 | 43609775 | |||||
chr20:43609775
|
CAA | C | 6 | a0001c0001t0001g0125a0001c0001t0001g0135a0001c0001t0001g0209others(3): Show | 6 | HG01169.hp1 HG02071.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.486-4052_486-4051d others(4): Show |
IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr20 | 43609775 | |||||
chr20:43609957
|
A | T | 2 | a0001c0002t0001g0004a0001c0002t0001g0019 | 3 | HG02723.hp2 HG02976.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.486-3893A>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | chr20 | 43609957 | ||||||
chr20:43609962
|
A | AAAATT | 5 | a0001c0001t0001g0259a0001c0001t0001g0260a0001c0001t0001g0261others(2): Show | 5 | HG02055.hp2 HG02895.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.486-3867_486-3863d others(7): Show |
IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr20 | 43609962 | |||||
chr20:43609962
|
A | T | 17 | a0001c0002t0001g0004a0001c0002t0001g0005a0001c0002t0001g0006others(14): Show | 20 | HG01109.hp2 HG02056.hp1 HG02135.hp2 others(17): Show |
intron_variant | MODIFIER | c.486-3888A>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | chr20 | 43609962 | ||||||
chr20:43609967
|
T | A | 34 | a0001c0001t0001g0117a0001c0001t0001g0119a0001c0001t0001g0120others(31): Show | 36 | HG01081.hp1 HG02040.hp1 HG02083.hp2 others(33): Show |
intron_variant | MODIFIER | c.486-3883T>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | chr20 | 43609967 | ||||||
chr20:43610111
|
C | A | 1 | a0001c0001t0001g0162 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.486-3739C>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | chr20 | 43610111 | ||||||
chr20:43610182
|
C | T | 180 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(177): Show | 187 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.486-3668C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | chr20 | 43610182 | ||||||
chr20:43610184
|
C | T | 1 | a0001c0002t0001g0079 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.486-3666C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | chr20 | 43610184 | ||||||
chr20:43610217
|
G | A | 180 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(177): Show | 187 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.486-3633G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | chr20 | 43610217 | ||||||
chr20:43610271
|
G | A | 1 | a0001c0001t0001g0247 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.486-3579G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | chr20 | 43610271 | ||||||
chr20:43610291
|
C | CA | 7 | a0001c0002t0001g0031a0001c0002t0001g0045a0001c0002t0001g0057others(4): Show | 7 | HG00544.hp2 HG01981.hp1 HG02027.hp1 others(4): Show |
intron_variant | MODIFIER | c.486-3542dupA | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr20 | 43610291 | |||||
chr20:43610291
|
CA | C | 174 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(171): Show | 186 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(183): Show |
intron_variant | MODIFIER | c.486-3542delA | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr20 | 43610291 | |||||
chr20:43610312
|
TA | T | 170 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(167): Show | 177 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(174): Show |
intron_variant | MODIFIER | c.486-3530delA | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr20 | 43610312 | |||||
chr20:43610447
|
A | T | 10 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0274others(7): Show | 10 | HG00741.hp2 HG01167.hp2 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.486-3403A>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | chr20 | 43610447 | ||||||
chr20:43610460
|
G | A | 235 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(232): Show | 249 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(246): Show |
intron_variant | MODIFIER | c.486-3390G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | chr20 | 43610460 | ||||||
chr20:43610505
|
A | G | 180 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(177): Show | 187 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.486-3345A>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | chr20 | 43610505 | ||||||
chr20:43610828
|
T | C | 30 | a0001c0002t0001g0009a0001c0002t0001g0010a0001c0002t0001g0017others(27): Show | 32 | HG01081.hp1 HG01884.hp1 HG02083.hp2 others(29): Show |
intron_variant | MODIFIER | c.486-3022T>C | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | chr20 | 43610828 | ||||||
chr20:43610917
|
T | C | 1 | a0001c0001t0001g0271 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.486-2933T>C | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | chr20 | 43610917 | ||||||
chr20:43611441
|
C | CT | 9 | a0001c0002t0001g0041a0001c0002t0001g0043a0001c0002t0001g0052others(6): Show | 9 | HG00544.hp2 HG01175.hp1 HG01361.hp2 others(6): Show |
intron_variant | MODIFIER | c.486-2382dupT | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr20 | 43611441 | |||||
chr20:43611441
|
CT | C | 34 | a0001c0002t0001g0004a0001c0002t0001g0005a0001c0002t0001g0009others(31): Show | 38 | HG01109.hp2 HG02056.hp1 HG02083.hp2 others(35): Show |
intron_variant | MODIFIER | c.486-2382delT | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr20 | 43611441 | |||||
chr20:43611441
|
CTT | C | 25 | a0001c0001t0001g0111a0001c0001t0001g0126a0001c0001t0001g0128others(22): Show | 25 | HG00438.hp1 HG00741.hp2 HG01167.hp1 others(22): Show |
intron_variant | MODIFIER | c.486-2383_486-2382d others(4): Show |
IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr20 | 43611441 | |||||
chr20:43611441
|
CTTT | C | 159 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(156): Show | 166 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.486-2384_486-2382d others(5): Show |
IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr20 | 43611441 | |||||
chr20:43611441
|
CTTTTTTT others(7): Show |
C | 1 | a0001c0006t0001g0016 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.486-2395_486-2382d others(16): Show |
IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr20 | 43611441 | |||||
chr20:43611598
|
C | T | 1 | a0006c0004t0001g0186 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.486-2252C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | chr20 | 43611598 | ||||||
chr20:43611599
|
G | A | 1 | a0001c0001t0001g0153 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.486-2251G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | chr20 | 43611599 | ||||||
chr20:43611729
|
G | A | 4 | a0001c0002t0001g0083a0001c0002t0001g0084a0001c0002t0001g0085others(1): Show | 4 | HG02717.hp1 HG02886.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.486-2121G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | chr20 | 43611729 | ||||||
chr20:43611757
|
C | A | 180 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(177): Show | 187 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.486-2093C>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | chr20 | 43611757 | ||||||
chr20:43611859
|
A | G | 2 | a0001c0001t0001g0236a0001c0001t0001g0237 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.486-1991A>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | chr20 | 43611859 | ||||||
chr20:43611964
|
A | T | 1 | a0001c0002t0001g0082 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.486-1886A>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | chr20 | 43611964 | ||||||
chr20:43612010
|
A | G | 1 | a0001c0001t0001g0271 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.486-1840A>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | chr20 | 43612010 | ||||||
chr20:43612090
|
G | A | 165 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(162): Show | 172 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(169): Show |
intron_variant | MODIFIER | c.486-1760G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | chr20 | 43612090 | ||||||
chr20:43612248
|
A | G | 1 | a0001c0001t0001g0119 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.486-1602A>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | chr20 | 43612248 | ||||||
chr20:43612707
|
A | ACAAT | 177 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(174): Show | 184 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(181): Show |
intron_variant | MODIFIER | c.486-1140_486-1139i others(6): Show |
IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr20 | 43612707 | |||||
chr20:43612707
|
A | T | 1 | a0001c0001t0001g0280 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.486-1143A>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | chr20 | 43612707 | ||||||
chr20:43612750
|
A | G | 1 | a0001c0003t0001g0022 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.486-1100A>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | chr20 | 43612750 | ||||||
chr20:43612754
|
G | T | 37 | a0001c0001t0001g0011a0001c0001t0001g0109a0001c0001t0001g0121others(34): Show | 38 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(35): Show |
intron_variant | MODIFIER | c.486-1096G>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | chr20 | 43612754 | ||||||
chr20:43612764
|
T | G | 1 | a0001c0001t0001g0271 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.486-1086T>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | chr20 | 43612764 | ||||||
chr20:43613171
|
G | A | 2 | a0001c0001t0001g0148a0001c0001t0001g0149 | 2 | HG00741.hp1 HG01257.hp2 |
intron_variant | MODIFIER | c.486-679G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | chr20 | 43613171 | ||||||
chr20:43613179
|
C | A | 4 | a0001c0003t0001g0002a0001c0003t0001g0021a0001c0003t0001g0022others(1): Show | 6 | HG01361.hp2 HG02615.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.486-671C>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | chr20 | 43613179 | ||||||
chr20:43613226
|
C | T | 11 | a0001c0001t0001g0003a0001c0001t0001g0131a0001c0001t0001g0134others(8): Show | 13 | HG00642.hp2 HG00733.hp1 HG00741.hp1 others(10): Show |
intron_variant | MODIFIER | c.486-624C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | chr20 | 43613226 | ||||||
chr20:43613311
|
C | T | 1 | a0001c0002t0001g0089 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.486-539C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | chr20 | 43613311 | ||||||
chr20:43613321
|
C | G | 1 | a0001c0006t0001g0016 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.486-529C>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | chr20 | 43613321 | ||||||
chr20:43613359
|
T | G | 2 | a0001c0001t0001g0207a0001c0001t0001g0210 | 2 | NA18973.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.486-491T>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | chr20 | 43613359 | ||||||
chr20:43613492
|
T | A | 1 | a0001c0001t0001g0166 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.486-358T>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | chr20 | 43613492 | ||||||
chr20:43613519
|
C | T | 1 | a0001c0002t0001g0082 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.486-331C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | chr20 | 43613519 | ||||||
chr20:43613716
|
C | A | 10 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0274others(7): Show | 10 | HG00741.hp2 HG01167.hp2 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.486-134C>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | chr20 | 43613716 | ||||||
chr20:43613812
|
T | A | 21 | a0001c0002t0001g0009a0001c0002t0001g0010a0001c0002t0001g0087others(18): Show | 23 | HG01081.hp1 HG02083.hp2 HG02486.hp2 others(20): Show |
intron_variant | MODIFIER | c.486-38T>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | chr20 | 43613812 | ||||||
chr20:43614060
|
C | T | 178 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(175): Show | 185 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.612+84C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 7/13 | chr20 | 43614060 | ||||||
chr20:43614303
|
C | T | 178 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(175): Show | 185 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.612+327C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 7/13 | chr20 | 43614303 | ||||||
chr20:43614342
|
C | T | 2 | a0001c0002t0001g0004a0001c0002t0001g0019 | 3 | HG02723.hp2 HG02976.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.612+366C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 7/13 | chr20 | 43614342 | ||||||
chr20:43614477
|
C | G | 1 | a0001c0001t0001g0241 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.612+501C>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 7/13 | chr20 | 43614477 | ||||||
chr20:43614481
|
G | A | 178 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(175): Show | 185 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.612+505G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 7/13 | chr20 | 43614481 | ||||||
chr20:43614546
|
G | T | 158 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(155): Show | 165 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.612+570G>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 7/13 | chr20 | 43614546 | ||||||
chr20:43614744
|
C | T | 4 | a0001c0001t0001g0128a0001c0001t0001g0164a0001c0001t0001g0179others(1): Show | 4 | HG00280.hp1 HG01175.hp2 HG02300.hp2 others(1): Show |
intron_variant | MODIFIER | c.612+768C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 7/13 | chr20 | 43614744 | ||||||
chr20:43614809
|
C | CT | 14 | a0001c0001t0001g0192a0001c0001t0001g0204a0001c0002t0001g0078others(11): Show | 16 | HG01361.hp2 HG02027.hp2 HG02602.hp2 others(13): Show |
intron_variant | MODIFIER | c.612+850dupT | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr20 | 43614809 | |||||
chr20:43614810
|
T | C | 1 | a0001c0001t0001g0271 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.612+834T>C | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 7/13 | chr20 | 43614810 | ||||||
chr20:43614923
|
C | T | 16 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0024others(13): Show | 18 | HG01109.hp2 HG02056.hp1 HG02135.hp1 others(15): Show |
intron_variant | MODIFIER | c.612+947C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 7/13 | chr20 | 43614923 | ||||||
chr20:43615165
|
T | C | 178 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(175): Show | 185 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.612+1189T>C | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 7/13 | chr20 | 43615165 | ||||||
chr20:43615177
|
G | A | 1 | a0001c0002t0001g0269 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.612+1201G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 7/13 | chr20 | 43615177 | ||||||
chr20:43615205
|
G | A | 12 | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0001t0001g0125others(9): Show | 12 | HG01891.hp2 HG02055.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.612+1229G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 7/13 | chr20 | 43615205 | ||||||
chr20:43615213
|
T | C | 3 | a0001c0002t0001g0106a0001c0002t0001g0107a0001c0002t0001g0108 | 3 | HG02602.hp2 HG02615.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.612+1237T>C | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 7/13 | chr20 | 43615213 | ||||||
chr20:43615223
|
A | G | 178 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(175): Show | 185 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.612+1247A>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 7/13 | chr20 | 43615223 | ||||||
chr20:43615287
|
C | T | 1 | a0001c0001t0001g0169 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.612+1311C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 7/13 | chr20 | 43615287 | ||||||
chr20:43615295
|
A | G | 1 | a0001c0002t0001g0019 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.612+1319A>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 7/13 | chr20 | 43615295 | ||||||
chr20:43615363
|
A | G | 168 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(165): Show | 175 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.612+1387A>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 7/13 | chr20 | 43615363 | ||||||
chr20:43615383
|
A | G | 3 | a0001c0002t0001g0106a0001c0002t0001g0107a0001c0002t0001g0108 | 3 | HG02602.hp2 HG02615.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.612+1407A>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 7/13 | chr20 | 43615383 | ||||||
chr20:43615619
|
C | T | 178 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(175): Show | 185 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.612+1643C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 7/13 | chr20 | 43615619 | ||||||
chr20:43615657
|
G | T | 178 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(175): Show | 185 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.612+1681G>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 7/13 | chr20 | 43615657 | ||||||
chr20:43615761
|
A | C | 1 | a0001c0001t0001g0271 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.612+1785A>C | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 7/13 | chr20 | 43615761 | ||||||
chr20:43615762
|
C | A | 1 | a0001c0001t0001g0271 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.612+1786C>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 7/13 | chr20 | 43615762 | ||||||
chr20:43615938
|
GA | G | 178 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(175): Show | 185 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.612+1972delA | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr20 | 43615938 | |||||
chr20:43616008
|
C | T | 1 | a0001c0006t0001g0016 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.612+2032C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 7/13 | chr20 | 43616008 | ||||||
chr20:43616043
|
A | T | 3 | a0001c0002t0001g0106a0001c0002t0001g0107a0001c0002t0001g0108 | 3 | HG02602.hp2 HG02615.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.612+2067A>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 7/13 | chr20 | 43616043 | ||||||
chr20:43616509
|
C | CA | 10 | a0001c0001t0001g0135a0001c0001t0001g0141a0001c0001t0001g0219others(7): Show | 10 | HG01934.hp2 HG01981.hp1 HG02071.hp1 others(7): Show |
intron_variant | MODIFIER | c.613-2414dupA | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr20 | 43616509 | |||||
chr20:43616509
|
CA | C | 8 | a0001c0001t0001g0114a0001c0002t0001g0082a0001c0002t0001g0093others(5): Show | 8 | HG01109.hp1 HG03486.hp1 NA18952.hp1 others(5): Show |
intron_variant | MODIFIER | c.613-2414delA | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr20 | 43616509 | |||||
chr20:43616660
|
T | C | 3 | a0001c0001t0001g0153a0001c0001t0001g0154a0001c0001t0001g0270 | 3 | HG01891.hp2 HG02976.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.613-2280T>C | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 7/13 | chr20 | 43616660 | ||||||
chr20:43616667
|
T | C | 4 | a0001c0002t0001g0083a0001c0002t0001g0084a0001c0002t0001g0085others(1): Show | 4 | HG02717.hp1 HG02886.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.613-2273T>C | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 7/13 | chr20 | 43616667 | ||||||
chr20:43616796
|
G | A | 21 | a0001c0002t0001g0009a0001c0002t0001g0010a0001c0002t0001g0087others(18): Show | 23 | HG01081.hp1 HG02083.hp2 HG02486.hp2 others(20): Show |
intron_variant | MODIFIER | c.613-2144G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 7/13 | chr20 | 43616796 | ||||||
chr20:43617343
|
A | G | 3 | a0001c0001t0001g0117a0001c0001t0001g0119a0001c0001t0001g0120 | 3 | HG02486.hp1 HG02886.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.613-1597A>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 7/13 | chr20 | 43617343 | ||||||
chr20:43617449
|
GT | G | 176 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(173): Show | 183 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(180): Show |
intron_variant | MODIFIER | c.613-1479delT | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr20 | 43617449 | |||||
chr20:43617450
|
T | G | 1 | a0001c0001t0001g0271 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.613-1490T>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 7/13 | chr20 | 43617450 | ||||||
chr20:43617479
|
T | G | 10 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0274others(7): Show | 10 | HG00741.hp2 HG01167.hp2 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.613-1461T>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 7/13 | chr20 | 43617479 | ||||||
chr20:43617494
|
G | T | 2 | a0001c0001t0001g0142a0001c0001t0001g0143 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.613-1446G>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 7/13 | chr20 | 43617494 | ||||||
chr20:43617558
|
C | G | 178 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(175): Show | 185 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.613-1382C>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 7/13 | chr20 | 43617558 | ||||||
chr20:43617591
|
G | A | 2 | a0001c0001t0001g0259a0001c0001t0001g0263 | 2 | HG02055.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.613-1349G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 7/13 | chr20 | 43617591 | ||||||
chr20:43617628
|
G | T | 1 | a0001c0002t0001g0082 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.613-1312G>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 7/13 | chr20 | 43617628 | ||||||
chr20:43617632
|
C | T | 4 | a0001c0003t0001g0002a0001c0003t0001g0021a0001c0003t0001g0022others(1): Show | 6 | HG01361.hp2 HG02615.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.613-1308C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 7/13 | chr20 | 43617632 | ||||||
chr20:43617644
|
A | G | 178 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(175): Show | 185 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.613-1296A>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 7/13 | chr20 | 43617644 | ||||||
chr20:43617664
|
G | A | 1 | a0001c0002t0001g0068 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.613-1276G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 7/13 | chr20 | 43617664 | ||||||
chr20:43617886
|
G | T | 4 | a0001c0003t0001g0002a0001c0003t0001g0021a0001c0003t0001g0022others(1): Show | 6 | HG01361.hp2 HG02615.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.613-1054G>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 7/13 | chr20 | 43617886 | ||||||
chr20:43618214
|
A | AT | 9 | a0001c0001t0001g0241a0001c0001t0001g0271a0001c0001t0001g0272others(6): Show | 9 | HG00741.hp2 HG01167.hp2 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.613-709dupT | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr20 | 43618214 | |||||
chr20:43618214
|
AT | A | 42 | a0001c0001t0001g0115a0001c0001t0001g0117a0001c0001t0001g0119others(39): Show | 44 | HG00323.hp1 HG00544.hp2 HG01069.hp1 others(41): Show |
intron_variant | MODIFIER | c.613-709delT | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr20 | 43618214 | |||||
chr20:43618214
|
ATT | A | 5 | a0001c0002t0001g0061a0001c0003t0001g0002a0001c0003t0001g0021others(2): Show | 7 | HG01361.hp2 HG02615.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.613-710_613-709del others(2): Show |
IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr20 | 43618214 | |||||
chr20:43618508
|
G | T | 2 | a0001c0002t0001g0004a0001c0002t0001g0019 | 3 | HG02723.hp2 HG02976.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.613-432G>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 7/13 | chr20 | 43618508 | ||||||
chr20:43618516
|
C | T | 168 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(165): Show | 175 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.613-424C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 7/13 | chr20 | 43618516 | ||||||
chr20:43618571
|
T | G | 1 | a0001c0002t0001g0033 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.613-369T>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 7/13 | chr20 | 43618571 | ||||||
chr20:43618584
|
C | T | 7 | a0001c0001t0001g0272a0001c0001t0001g0277a0001c0001t0001g0278others(4): Show | 7 | HG00741.hp2 HG01167.hp2 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.613-356C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 7/13 | chr20 | 43618584 | ||||||
chr20:43618648
|
A | ATT | 178 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(175): Show | 185 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.613-284_613-283dup others(2): Show |
IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr20 | 43618648 | |||||
chr20:43618714
|
C | G | 1 | a0001c0001t0001g0245 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.613-226C>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 7/13 | chr20 | 43618714 | ||||||
chr20:43618736
|
G | A | 4 | a0001c0002t0001g0083a0001c0002t0001g0084a0001c0002t0001g0085others(1): Show | 4 | HG02717.hp1 HG02886.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.613-204G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 7/13 | chr20 | 43618736 | ||||||
chr20:43618775
|
G | A | 6 | a0001c0001t0001g0258a0001c0001t0001g0259a0001c0001t0001g0260others(3): Show | 6 | HG01243.hp2 HG02055.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.613-165G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 7/13 | chr20 | 43618775 | ||||||
chr20:43619166
|
C | T | 4 | a0001c0001t0001g0138a0001c0001t0001g0184a0001c0001t0001g0203others(1): Show | 4 | HG00735.hp1 HG01074.hp2 HG01081.hp2 others(1): Show |
intron_variant | MODIFIER | c.699+140C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 8/13 | chr20 | 43619166 | ||||||
chr20:43619167
|
GAGTCAGG others(3): Show |
G | 1 | a0001c0001t0001g0212 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.699+146_699+155del others(10): Show |
IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr20 | 43619167 | |||||
chr20:43619517
|
A | G | 1 | a0001c0002t0001g0082 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.699+491A>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 8/13 | chr20 | 43619517 | ||||||
chr20:43619576
|
G | C | 4 | a0001c0003t0001g0002a0001c0003t0001g0021a0001c0003t0001g0022others(1): Show | 6 | HG01361.hp2 HG02615.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.699+550G>C | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 8/13 | chr20 | 43619576 | ||||||
chr20:43619631
|
G | A | 19 | a0001c0002t0001g0008a0001c0002t0001g0054a0001c0002t0001g0056others(16): Show | 20 | HG00544.hp2 HG01496.hp1 HG01934.hp2 others(17): Show |
intron_variant | MODIFIER | c.699+605G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 8/13 | chr20 | 43619631 | ||||||
chr20:43619727
|
A | G | 1 | a0001c0002t0001g0269 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.699+701A>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 8/13 | chr20 | 43619727 | ||||||
chr20:43619910
|
C | CT | 160 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(157): Show | 170 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(167): Show |
intron_variant | MODIFIER | c.699+908dupT | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr20 | 43619910 | |||||
chr20:43619910
|
C | CTT | 31 | a0001c0001t0001g0118a0001c0001t0001g0120a0001c0001t0001g0126others(28): Show | 33 | HG00597.hp2 HG01109.hp2 HG02055.hp2 others(30): Show |
intron_variant | MODIFIER | c.699+907_699+908dup others(2): Show |
IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr20 | 43619910 | |||||
chr20:43619910
|
CT | C | 27 | a0001c0002t0001g0009a0001c0002t0001g0010a0001c0002t0001g0017others(24): Show | 29 | HG01884.hp1 HG02027.hp1 HG02083.hp2 others(26): Show |
intron_variant | MODIFIER | c.699+908delT | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr20 | 43619910 | |||||
chr20:43619982
|
C | T | 216 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(213): Show | 228 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.700-875C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 8/13 | chr20 | 43619982 | ||||||
chr20:43620020
|
G | A | 1 | a0001c0001t0001g0191 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.700-837G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 8/13 | chr20 | 43620020 | ||||||
chr20:43620026
|
C | T | 167 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(164): Show | 174 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.700-831C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 8/13 | chr20 | 43620026 | ||||||
chr20:43620117
|
A | G | 1 | a0001c0001t0001g0280 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.700-740A>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 8/13 | chr20 | 43620117 | ||||||
chr20:43620208
|
T | A | 177 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(174): Show | 184 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(181): Show |
intron_variant | MODIFIER | c.700-649T>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 8/13 | chr20 | 43620208 | ||||||
chr20:43620421
|
G | A | 1 | a0001c0001t0001g0221 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.700-436G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 8/13 | chr20 | 43620421 | ||||||
chr20:43620545
|
C | A | 177 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(174): Show | 184 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(181): Show |
intron_variant | MODIFIER | c.700-312C>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 8/13 | chr20 | 43620545 | ||||||
chr20:43620571
|
G | A | 1 | a0001c0002t0001g0042 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.700-286G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 8/13 | chr20 | 43620571 | ||||||
chr20:43620571
|
G | T | 1 | a0001c0002t0001g0019 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.700-286G>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 8/13 | chr20 | 43620571 | ||||||
chr20:43620758
|
C | T | 216 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(213): Show | 228 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.700-99C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 8/13 | chr20 | 43620758 | ||||||
chr20:43620839
|
C | CT | 186 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(183): Show | 194 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(191): Show |
splice_region_variant&intron_variant | LOW | c.700-8dupT | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr20 | 43620839 | |||||
chr20:43620849
|
T | TA | 4 | a0001c0001t0001g0114a0001c0001t0001g0172a0001c0001t0001g0252others(1): Show | 4 | HG00597.hp1 HG01109.hp1 NA18951.hp2 others(1): Show |
splice_region_variant&intron_variant | LOW | c.700-6dupA | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr20 | 43620849 | |||||
chr20:43621202
|
T | C | 1 | a0001c0002t0001g0039 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.768+277T>C | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 9/13 | chr20 | 43621202 | ||||||
chr20:43621765
|
C | T | 1 | a0001c0006t0001g0016 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.768+840C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 9/13 | chr20 | 43621765 | ||||||
chr20:43621802
|
C | T | 215 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(212): Show | 227 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(224): Show |
intron_variant | MODIFIER | c.768+877C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 9/13 | chr20 | 43621802 | ||||||
chr20:43622442
|
CA | C | 167 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(164): Show | 174 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.769-1438delA | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr20 | 43622442 | |||||
chr20:43622538
|
G | A | 1 | a0001c0001t0001g0136 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.769-1353G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 9/13 | chr20 | 43622538 | ||||||
chr20:43622660
|
A | ATATGTAA others(20): Show |
1 | a0001c0002t0001g0065 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.769-1202_769-1176d others(29): Show |
IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr20 | 43622660 | |||||
chr20:43622684
|
A | ATTTTATG others(21): Show |
1 | a0003c0008t0001g0034 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.769-1153_769-1126d others(30): Show |
IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr20 | 43622684 | |||||
chr20:43622711
|
AT | A | 10 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0274others(7): Show | 10 | HG00741.hp2 HG01167.hp2 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.769-1175delT | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr20 | 43622711 | |||||
chr20:43622715
|
TTATGTAA others(78): Show |
T | 1 | a0002c0009t0001g0020 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.769-1142_769-1058d others(87): Show |
IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr20 | 43622715 | |||||
chr20:43622739
|
AT | A | 10 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0274others(7): Show | 10 | HG00741.hp2 HG01167.hp2 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.769-1147delT | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr20 | 43622739 | |||||
chr20:43622745
|
ATGTAAAT others(20): Show |
A | 5 | a0001c0001t0001g0111a0001c0001t0001g0113a0001c0001t0001g0167others(2): Show | 5 | HG00738.hp1 HG02280.hp1 HG03239.hp2 others(2): Show |
intron_variant | MODIFIER | c.769-1125_769-1099d others(29): Show |
IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr20 | 43622745 | |||||
chr20:43622765
|
A | AT | 161 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(158): Show | 168 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(165): Show |
intron_variant | MODIFIER | c.769-1126_769-1125i others(3): Show |
IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 9/13 | chr20 | 43622765 | ||||||
chr20:43622765
|
A | ATATTTTT others(22): Show |
11 | a0001c0001t0001g0118a0001c0001t0001g0123a0001c0001t0001g0132others(8): Show | 11 | HG00099.hp1 HG01106.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.769-1126_769-1125i others(31): Show |
IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 9/13 | chr20 | 43622765 | ||||||
chr20:43622766
|
A | T | 4 | a0001c0002t0001g0083a0001c0002t0001g0084a0001c0002t0001g0085others(1): Show | 4 | HG02717.hp1 HG02886.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.769-1125A>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 9/13 | chr20 | 43622766 | ||||||
chr20:43622767
|
A | ATT | 34 | a0001c0002t0001g0004a0001c0002t0001g0009a0001c0002t0001g0010others(31): Show | 39 | HG01081.hp1 HG01361.hp2 HG01884.hp1 others(36): Show |
intron_variant | MODIFIER | c.769-1123_769-1122d others(4): Show |
IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr20 | 43622767 | |||||
chr20:43622767
|
A | ATTTTTAT others(23): Show |
4 | a0001c0002t0001g0083a0001c0002t0001g0084a0001c0002t0001g0085others(1): Show | 4 | HG02717.hp1 HG02886.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.769-1122_769-1121i others(32): Show |
IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr20 | 43622767 | |||||
chr20:43622767
|
A | T | 172 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(169): Show | 179 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(176): Show |
intron_variant | MODIFIER | c.769-1124A>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 9/13 | chr20 | 43622767 | ||||||
chr20:43622770
|
G | A | 38 | a0001c0002t0001g0004a0001c0002t0001g0009a0001c0002t0001g0010others(35): Show | 43 | HG01081.hp1 HG01361.hp2 HG01884.hp1 others(40): Show |
intron_variant | MODIFIER | c.769-1121G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 9/13 | chr20 | 43622770 | ||||||
chr20:43622770
|
G | T | 232 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(229): Show | 245 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(242): Show |
intron_variant | MODIFIER | c.769-1121G>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 9/13 | chr20 | 43622770 | ||||||
chr20:43622772
|
G | A | 172 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(169): Show | 179 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(176): Show |
intron_variant | MODIFIER | c.769-1119G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 9/13 | chr20 | 43622772 | ||||||
chr20:43622802
|
A | ATGTAAAT others(23): Show |
1 | a0001c0002t0001g0082 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.769-1065_769-1036d others(32): Show |
IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr20 | 43622802 | |||||
chr20:43622802
|
A | G | 42 | a0001c0001t0001g0013a0001c0001t0001g0015a0001c0001t0001g0110others(39): Show | 44 | HG00323.hp2 HG00544.hp1 HG00735.hp1 others(41): Show |
intron_variant | MODIFIER | c.769-1089A>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 9/13 | chr20 | 43622802 | ||||||
chr20:43623190
|
A | G | 6 | a0001c0001t0001g0258a0001c0001t0001g0259a0001c0001t0001g0260others(3): Show | 6 | HG01243.hp2 HG02055.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.769-701A>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 9/13 | chr20 | 43623190 | ||||||
chr20:43623507
|
G | C | 2 | a0001c0001t0001g0111a0001c0001t0001g0113 | 2 | HG00738.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.769-384G>C | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 9/13 | chr20 | 43623507 | ||||||
chr20:43623555
|
G | A | 2 | a0001c0006t0001g0016a0002c0009t0001g0020 | 2 | NA18906.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.769-336G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 9/13 | chr20 | 43623555 | ||||||
chr20:43623685
|
G | T | 177 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(174): Show | 184 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(181): Show |
intron_variant | MODIFIER | c.769-206G>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 9/13 | chr20 | 43623685 | ||||||
chr20:43624215
|
T | G | 4 | a0001c0003t0001g0002a0001c0003t0001g0021a0001c0003t0001g0022others(1): Show | 6 | HG01361.hp2 HG02615.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.923+170T>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43624215 | ||||||
chr20:43624548
|
G | A | 2 | a0001c0001t0001g0141a0001c0001t0001g0216 | 2 | HG03669.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.923+503G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43624548 | ||||||
chr20:43624560
|
G | A | 3 | a0001c0002t0001g0106a0001c0002t0001g0107a0001c0002t0001g0108 | 3 | HG02602.hp2 HG02615.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.923+515G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43624560 | ||||||
chr20:43624681
|
A | G | 2 | a0001c0006t0001g0016a0002c0009t0001g0020 | 2 | NA18906.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.923+636A>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43624681 | ||||||
chr20:43624707
|
G | A | 1 | a0005c0007t0001g0095 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.923+662G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43624707 | ||||||
chr20:43624902
|
A | G | 179 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(176): Show | 186 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(183): Show |
intron_variant | MODIFIER | c.923+857A>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43624902 | ||||||
chr20:43624975
|
G | A | 1 | a0001c0002t0001g0004 | 2 | HG02723.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.923+930G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43624975 | ||||||
chr20:43625215
|
A | T | 216 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(213): Show | 228 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.923+1170A>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43625215 | ||||||
chr20:43625255
|
A | G | 1 | a0001c0001t0001g0255 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.923+1210A>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43625255 | ||||||
chr20:43625258
|
C | A | 171 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(168): Show | 178 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(175): Show |
intron_variant | MODIFIER | c.923+1213C>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43625258 | ||||||
chr20:43625315
|
C | A | 3 | a0001c0002t0001g0106a0001c0002t0001g0107a0001c0002t0001g0108 | 3 | HG02602.hp2 HG02615.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.923+1270C>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43625315 | ||||||
chr20:43625564
|
A | G | 1 | a0001c0001t0001g0137 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.923+1519A>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43625564 | ||||||
chr20:43625635
|
C | T | 4 | a0001c0002t0001g0083a0001c0002t0001g0084a0001c0002t0001g0085others(1): Show | 4 | HG02717.hp1 HG02886.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.923+1590C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43625635 | ||||||
chr20:43625684
|
A | G | 3 | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0001t0001g0125 | 3 | HG02055.hp1 HG02809.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.923+1639A>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43625684 | ||||||
chr20:43625798
|
A | G | 3 | a0001c0002t0001g0106a0001c0002t0001g0107a0001c0002t0001g0108 | 3 | HG02602.hp2 HG02615.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.923+1753A>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43625798 | ||||||
chr20:43625801
|
A | AGAG | 11 | a0001c0001t0001g0012a0001c0001t0001g0133a0001c0001t0001g0139others(8): Show | 12 | HG02027.hp2 HG02132.hp1 HG04184.hp2 others(9): Show |
intron_variant | MODIFIER | c.923+1760_923+1762d others(5): Show |
IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr20 | 43625801 | |||||
chr20:43626022
|
G | GA | 183 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(180): Show | 192 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(189): Show |
intron_variant | MODIFIER | c.923+1998dupA | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr20 | 43626022 | |||||
chr20:43626022
|
G | GAA | 21 | a0001c0001t0001g0111a0001c0001t0001g0120a0001c0001t0001g0147others(18): Show | 21 | HG00099.hp1 HG00438.hp2 HG00642.hp2 others(18): Show |
intron_variant | MODIFIER | c.923+1997_923+1998d others(4): Show |
IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr20 | 43626022 | |||||
chr20:43626077
|
A | G | 4 | a0001c0001t0001g0134a0001c0001t0001g0144a0001c0001t0001g0145others(1): Show | 4 | HG00642.hp2 HG01074.hp1 HG01361.hp1 others(1): Show |
intron_variant | MODIFIER | c.923+2032A>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43626077 | ||||||
chr20:43626187
|
A | G | 1 | a0001c0001t0001g0123 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.923+2142A>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43626187 | ||||||
chr20:43626243
|
A | C | 3 | a0001c0002t0001g0106a0001c0002t0001g0107a0001c0002t0001g0108 | 3 | HG02602.hp2 HG02615.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.923+2198A>C | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43626243 | ||||||
chr20:43626466
|
G | A | 3 | a0001c0002t0001g0106a0001c0002t0001g0107a0001c0002t0001g0108 | 3 | HG02602.hp2 HG02615.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.923+2421G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43626466 | ||||||
chr20:43626622
|
C | T | 3 | a0001c0002t0001g0106a0001c0002t0001g0107a0001c0002t0001g0108 | 3 | HG02602.hp2 HG02615.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.923+2577C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43626622 | ||||||
chr20:43626797
|
AAGTGTTG others(2): Show |
A | 158 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(155): Show | 165 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.923+2755_923+2763d others(11): Show |
IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr20 | 43626797 | |||||
chr20:43626862
|
T | G | 17 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0024others(14): Show | 19 | HG01109.hp2 HG02056.hp1 HG02135.hp1 others(16): Show |
intron_variant | MODIFIER | c.923+2817T>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43626862 | ||||||
chr20:43627039
|
C | T | 1 | a0001c0002t0001g0027 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.923+2994C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43627039 | ||||||
chr20:43627091
|
C | T | 3 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0253 | 3 | HG01433.hp2 HG03834.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.923+3046C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43627091 | ||||||
chr20:43627162
|
A | G | 2 | a0001c0006t0001g0016a0002c0009t0001g0020 | 2 | NA18906.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.923+3117A>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43627162 | ||||||
chr20:43627170
|
A | G | 165 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(162): Show | 172 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(169): Show |
intron_variant | MODIFIER | c.923+3125A>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43627170 | ||||||
chr20:43627171
|
A | G | 1 | a0001c0001t0001g0260 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.923+3126A>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43627171 | ||||||
chr20:43627224
|
G | A | 167 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(164): Show | 174 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.923+3179G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43627224 | ||||||
chr20:43627274
|
A | G | 3 | a0001c0002t0001g0106a0001c0002t0001g0107a0001c0002t0001g0108 | 3 | HG02602.hp2 HG02615.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.923+3229A>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43627274 | ||||||
chr20:43627281
|
G | A | 1 | a0001c0001t0001g0172 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.923+3236G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43627281 | ||||||
chr20:43627402
|
C | G | 1 | a0001c0001t0001g0212 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.923+3357C>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43627402 | ||||||
chr20:43627489
|
T | G | 1 | a0001c0002t0001g0091 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.923+3444T>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43627489 | ||||||
chr20:43627596
|
A | C | 4 | a0001c0001t0001g0188a0001c0001t0001g0202a0001c0001t0001g0207others(1): Show | 4 | NA18973.hp1 NA18975.hp2 NA18995.hp2 others(1): Show |
intron_variant | MODIFIER | c.923+3551A>C | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43627596 | ||||||
chr20:43627805
|
C | A | 2 | a0001c0001t0001g0169a0001c0001t0001g0242 | 2 | HG02683.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.923+3760C>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43627805 | ||||||
chr20:43627904
|
T | G | 1 | a0002c0009t0001g0020 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.923+3859T>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43627904 | ||||||
chr20:43627904
|
TAG | T | 72 | a0001c0001t0001g0142a0001c0001t0001g0143a0001c0001t0001g0206others(69): Show | 83 | HG00323.hp2 HG00544.hp2 HG00642.hp1 others(80): Show |
intron_variant | MODIFIER | c.923+3876_923+3877d others(4): Show |
IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr20 | 43627904 | |||||
chr20:43627906
|
G | T | 81 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0109others(78): Show | 84 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(81): Show |
intron_variant | MODIFIER | c.923+3861G>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43627906 | ||||||
chr20:43627908
|
G | T | 31 | a0001c0001t0001g0142a0001c0001t0001g0143a0001c0002t0001g0001others(28): Show | 34 | HG00544.hp2 HG00642.hp1 HG01069.hp1 others(31): Show |
intron_variant | MODIFIER | c.923+3863G>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43627908 | ||||||
chr20:43627914
|
G | A | 8 | a0001c0002t0001g0017a0001c0002t0001g0018a0001c0002t0001g0083others(5): Show | 8 | HG01884.hp1 HG02630.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.923+3869G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43627914 | ||||||
chr20:43627916
|
G | A | 19 | a0001c0002t0001g0009a0001c0002t0001g0010a0001c0002t0001g0087others(16): Show | 21 | HG01081.hp1 HG02083.hp2 HG02486.hp2 others(18): Show |
intron_variant | MODIFIER | c.923+3871G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43627916 | ||||||
chr20:43627920
|
G | GT | 6 | a0001c0001t0001g0182a0001c0001t0001g0258a0001c0001t0001g0259others(3): Show | 6 | HG01243.hp1 HG01243.hp2 HG01261.hp1 others(3): Show |
intron_variant | MODIFIER | c.923+3875_923+3876i others(3): Show |
IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43627920 | ||||||
chr20:43627920
|
GA | G | 154 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(151): Show | 161 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(158): Show |
intron_variant | MODIFIER | c.923+3876delA | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43627920 | ||||||
chr20:43627920
|
GAGT | G | 9 | a0001c0002t0001g0017a0001c0002t0001g0018a0001c0002t0001g0029others(6): Show | 9 | HG01884.hp1 HG02630.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.923+3876_923+3878d others(5): Show |
IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43627920 | ||||||
chr20:43627921
|
A | T | 36 | a0001c0001t0001g0116a0001c0001t0001g0128a0001c0001t0001g0147others(33): Show | 36 | HG00597.hp1 HG00642.hp2 HG00741.hp2 others(33): Show |
intron_variant | MODIFIER | c.923+3876A>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43627921 | ||||||
chr20:43627922
|
G | T | 187 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(184): Show | 194 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.923+3877G>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43627922 | ||||||
chr20:43627990
|
G | A | 167 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(164): Show | 174 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.923+3945G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43627990 | ||||||
chr20:43628219
|
AC | A | 10 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0274others(7): Show | 10 | HG00741.hp2 HG01167.hp2 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.923+4175delC | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43628219 | ||||||
chr20:43628225
|
A | G | 233 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(230): Show | 247 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.923+4180A>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43628225 | ||||||
chr20:43628363
|
G | A | 1 | a0001c0002t0001g0077 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.923+4318G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43628363 | ||||||
chr20:43628428
|
G | A | 9 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0132others(6): Show | 9 | HG01168.hp1 HG01169.hp1 HG02074.hp1 others(6): Show |
intron_variant | MODIFIER | c.923+4383G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43628428 | ||||||
chr20:43628854
|
C | CA | 166 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(163): Show | 173 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.923+4821dupA | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr20 | 43628854 | |||||
chr20:43628990
|
T | C | 1 | a0001c0001t0001g0208 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.923+4945T>C | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43628990 | ||||||
chr20:43629348
|
CT | C | 158 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(155): Show | 165 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.923+5304delT | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43629348 | ||||||
chr20:43629351
|
C | T | 158 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(155): Show | 165 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.923+5306C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43629351 | ||||||
chr20:43629352
|
A | G | 158 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(155): Show | 165 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.923+5307A>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43629352 | ||||||
chr20:43629354
|
GCTCC | G | 158 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(155): Show | 165 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.923+5310_923+5313d others(6): Show |
IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43629354 | ||||||
chr20:43629359
|
G | A | 6 | a0001c0002t0001g0017a0001c0002t0001g0018a0001c0002t0001g0083others(3): Show | 6 | HG01884.hp1 HG02630.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.923+5314G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43629359 | ||||||
chr20:43629417
|
C | T | 1 | a0001c0002t0001g0017 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.923+5372C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43629417 | ||||||
chr20:43629500
|
C | A | 177 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(174): Show | 184 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(181): Show |
intron_variant | MODIFIER | c.923+5455C>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43629500 | ||||||
chr20:43629510
|
T | G | 233 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(230): Show | 247 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.923+5465T>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43629510 | ||||||
chr20:43629523
|
C | T | 4 | a0001c0003t0001g0002a0001c0003t0001g0021a0001c0003t0001g0022others(1): Show | 6 | HG01361.hp2 HG02615.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.923+5478C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43629523 | ||||||
chr20:43629916
|
C | T | 1 | a0001c0001t0001g0203 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.923+5871C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43629916 | ||||||
chr20:43630012
|
G | A | 1 | a0001c0002t0001g0027 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.924-5914G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43630012 | ||||||
chr20:43630022
|
T | A | 50 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0014others(47): Show | 54 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(51): Show |
intron_variant | MODIFIER | c.924-5904T>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43630022 | ||||||
chr20:43630095
|
ACAG | A | 21 | a0001c0002t0001g0009a0001c0002t0001g0010a0001c0002t0001g0087others(18): Show | 23 | HG01081.hp1 HG02083.hp2 HG02486.hp2 others(20): Show |
intron_variant | MODIFIER | c.924-5829_924-5827d others(5): Show |
IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr20 | 43630095 | |||||
chr20:43630232
|
C | T | 1 | a0001c0001t0001g0235 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.924-5694C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43630232 | ||||||
chr20:43630320
|
C | T | 176 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(173): Show | 183 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(180): Show |
intron_variant | MODIFIER | c.924-5606C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43630320 | ||||||
chr20:43630476
|
T | G | 1 | a0001c0002t0001g0004 | 2 | HG02723.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.924-5450T>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43630476 | ||||||
chr20:43630558
|
G | GTCAACTA others(6): Show |
1 | a0001c0002t0001g0063 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.924-5367_924-5355d others(15): Show |
IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr20 | 43630558 | |||||
chr20:43630614
|
A | G | 1 | a0001c0001t0001g0140 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.924-5312A>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43630614 | ||||||
chr20:43630645
|
G | A | 1 | a0001c0001t0001g0218 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.924-5281G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43630645 | ||||||
chr20:43630662
|
T | A | 1 | a0001c0002t0001g0063 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.924-5264T>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43630662 | ||||||
chr20:43630680
|
T | A | 1 | a0001c0002t0001g0063 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.924-5246T>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43630680 | ||||||
chr20:43630780
|
G | A | 1 | a0001c0002t0001g0063 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.924-5146G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43630780 | ||||||
chr20:43630837
|
G | A | 6 | a0001c0001t0001g0258a0001c0001t0001g0259a0001c0001t0001g0260others(3): Show | 6 | HG01243.hp2 HG02055.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.924-5089G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43630837 | ||||||
chr20:43630996
|
T | C | 216 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(213): Show | 228 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.924-4930T>C | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43630996 | ||||||
chr20:43631074
|
T | C | 1 | a0001c0001t0001g0273 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.924-4852T>C | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43631074 | ||||||
chr20:43631141
|
T | A | 1 | a0001c0002t0001g0063 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.924-4785T>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43631141 | ||||||
chr20:43631292
|
A | G | 2 | a0001c0006t0001g0016a0002c0009t0001g0020 | 2 | NA18906.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.924-4634A>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43631292 | ||||||
chr20:43631380
|
AC | A | 2 | a0001c0002t0001g0004a0001c0002t0001g0019 | 3 | HG02723.hp2 HG02976.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.924-4544delC | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr20 | 43631380 | |||||
chr20:43631446
|
T | C | 1 | a0001c0002t0001g0269 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.924-4480T>C | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43631446 | ||||||
chr20:43631478
|
T | A | 1 | a0001c0002t0001g0063 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.924-4448T>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43631478 | ||||||
chr20:43631519
|
G | A | 6 | a0001c0002t0001g0017a0001c0002t0001g0018a0001c0002t0001g0083others(3): Show | 6 | HG01884.hp1 HG02630.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.924-4407G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43631519 | ||||||
chr20:43631607
|
T | C | 158 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(155): Show | 165 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.924-4319T>C | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43631607 | ||||||
chr20:43631635
|
T | A | 1 | a0001c0002t0001g0063 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.924-4291T>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43631635 | ||||||
chr20:43631693
|
G | A | 1 | a0001c0001t0001g0139 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.924-4233G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43631693 | ||||||
chr20:43631801
|
G | C | 17 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0024others(14): Show | 19 | HG01109.hp2 HG02056.hp1 HG02135.hp1 others(16): Show |
intron_variant | MODIFIER | c.924-4125G>C | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43631801 | ||||||
chr20:43631828
|
A | T | 1 | a0001c0002t0001g0063 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.924-4098A>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43631828 | ||||||
chr20:43631924
|
C | CT | 15 | a0001c0001t0001g0267a0001c0001t0001g0277a0001c0002t0001g0004others(12): Show | 18 | HG00735.hp2 HG01167.hp2 HG01361.hp2 others(15): Show |
intron_variant | MODIFIER | c.924-3984dupT | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr20 | 43631924 | |||||
chr20:43631924
|
CT | C | 6 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0165others(3): Show | 6 | HG01168.hp1 HG02818.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.924-3984delT | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr20 | 43631924 | |||||
chr20:43631931
|
T | A | 1 | a0001c0002t0001g0063 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.924-3995T>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43631931 | ||||||
chr20:43632050
|
C | T | 233 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(230): Show | 247 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.924-3876C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43632050 | ||||||
chr20:43632095
|
T | A | 1 | a0001c0002t0001g0063 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.924-3831T>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43632095 | ||||||
chr20:43632113
|
C | T | 1 | a0001c0001t0001g0127 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.924-3813C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43632113 | ||||||
chr20:43632122
|
T | A | 1 | a0001c0002t0001g0063 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.924-3804T>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43632122 | ||||||
chr20:43632167
|
C | T | 3 | a0001c0002t0001g0106a0001c0002t0001g0107a0001c0002t0001g0108 | 3 | HG02602.hp2 HG02615.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.924-3759C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43632167 | ||||||
chr20:43632205
|
G | A | 3 | a0001c0002t0001g0106a0001c0002t0001g0107a0001c0002t0001g0108 | 3 | HG02602.hp2 HG02615.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.924-3721G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43632205 | ||||||
chr20:43632294
|
T | A | 1 | a0001c0002t0001g0063 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.924-3632T>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43632294 | ||||||
chr20:43632313
|
T | C | 2 | a0001c0001t0001g0213a0001c0001t0001g0267 | 2 | HG02040.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.924-3613T>C | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43632313 | ||||||
chr20:43632410
|
G | A | 1 | a0001c0001t0001g0258 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.924-3516G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43632410 | ||||||
chr20:43632505
|
C | T | 19 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0024others(16): Show | 21 | HG01109.hp2 HG02056.hp1 HG02135.hp1 others(18): Show |
intron_variant | MODIFIER | c.924-3421C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43632505 | ||||||
chr20:43632657
|
C | A | 1 | a0001c0002t0001g0063 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.924-3269C>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43632657 | ||||||
chr20:43632835
|
G | T | 10 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0274others(7): Show | 10 | HG00741.hp2 HG01167.hp2 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.924-3091G>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43632835 | ||||||
chr20:43632909
|
T | A | 1 | a0001c0002t0001g0063 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.924-3017T>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43632909 | ||||||
chr20:43632936
|
T | C | 1 | a0001c0002t0001g0025 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.924-2990T>C | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43632936 | ||||||
chr20:43632995
|
C | CATTT | 27 | a0001c0002t0001g0009a0001c0002t0001g0010a0001c0002t0001g0017others(24): Show | 29 | HG01081.hp1 HG01884.hp1 HG02083.hp2 others(26): Show |
intron_variant | MODIFIER | c.924-2930_924-2927d others(6): Show |
IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr20 | 43632995 | |||||
chr20:43633053
|
T | A | 2 | a0001c0006t0001g0016a0002c0009t0001g0020 | 2 | NA18906.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.924-2873T>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43633053 | ||||||
chr20:43633089
|
A | G | 1 | a0002c0009t0001g0020 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.924-2837A>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43633089 | ||||||
chr20:43633179
|
A | T | 1 | a0001c0002t0001g0063 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.924-2747A>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43633179 | ||||||
chr20:43633189
|
C | A | 17 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0024others(14): Show | 19 | HG01109.hp2 HG02056.hp1 HG02135.hp1 others(16): Show |
intron_variant | MODIFIER | c.924-2737C>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43633189 | ||||||
chr20:43633267
|
C | T | 4 | a0001c0003t0001g0002a0001c0003t0001g0021a0001c0003t0001g0022others(1): Show | 6 | HG01361.hp2 HG02615.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.924-2659C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43633267 | ||||||
chr20:43633291
|
C | T | 4 | a0001c0001t0001g0185a0001c0001t0001g0187a0001c0001t0001g0201others(1): Show | 4 | HG00544.hp1 HG01981.hp2 HG01993.hp2 others(1): Show |
intron_variant | MODIFIER | c.924-2635C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43633291 | ||||||
chr20:43633304
|
T | A | 1 | a0001c0002t0001g0063 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.924-2622T>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43633304 | ||||||
chr20:43633359
|
A | C | 10 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0274others(7): Show | 10 | HG00741.hp2 HG01167.hp2 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.924-2567A>C | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43633359 | ||||||
chr20:43633553
|
C | A | 1 | a0001c0002t0001g0063 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.924-2373C>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43633553 | ||||||
chr20:43633581
|
G | A | 4 | a0001c0003t0001g0002a0001c0003t0001g0021a0001c0003t0001g0022others(1): Show | 6 | HG01361.hp2 HG02615.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.924-2345G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43633581 | ||||||
chr20:43633626
|
T | A | 1 | a0001c0002t0001g0063 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.924-2300T>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43633626 | ||||||
chr20:43633697
|
G | T | 1 | a0001c0001t0001g0215 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.924-2229G>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43633697 | ||||||
chr20:43633831
|
A | T | 1 | a0001c0002t0001g0063 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.924-2095A>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43633831 | ||||||
chr20:43633832
|
T | A | 1 | a0001c0002t0001g0063 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.924-2094T>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43633832 | ||||||
chr20:43633927
|
G | A | 1 | a0001c0002t0001g0004 | 2 | HG02723.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.924-1999G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43633927 | ||||||
chr20:43633954
|
A | G | 2 | a0001c0006t0001g0016a0002c0009t0001g0020 | 2 | NA18906.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.924-1972A>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43633954 | ||||||
chr20:43633980
|
A | T | 1 | a0001c0002t0001g0063 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.924-1946A>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43633980 | ||||||
chr20:43634024
|
C | T | 1 | a0001c0001t0001g0196 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.924-1902C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43634024 | ||||||
chr20:43634055
|
C | A | 1 | a0001c0002t0001g0063 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.924-1871C>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43634055 | ||||||
chr20:43634175
|
T | A | 1 | a0001c0002t0001g0063 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.924-1751T>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43634175 | ||||||
chr20:43634214
|
GA | G | 257 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(254): Show | 272 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(269): Show |
intron_variant | MODIFIER | c.924-1701delA | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr20 | 43634214 | |||||
chr20:43634228
|
G | A | 171 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(168): Show | 178 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(175): Show |
intron_variant | MODIFIER | c.924-1698G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43634228 | ||||||
chr20:43634367
|
T | A | 1 | a0001c0002t0001g0063 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.924-1559T>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43634367 | ||||||
chr20:43634372
|
TAAATCAA others(3): Show |
T | 1 | a0001c0002t0001g0063 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.924-1550_924-1541d others(12): Show |
IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr20 | 43634372 | |||||
chr20:43634401
|
A | G | 4 | a0001c0002t0001g0083a0001c0002t0001g0084a0001c0002t0001g0085others(1): Show | 4 | HG02717.hp1 HG02886.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.924-1525A>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43634401 | ||||||
chr20:43634424
|
C | T | 3 | a0001c0002t0001g0106a0001c0002t0001g0107a0001c0002t0001g0108 | 3 | HG02602.hp2 HG02615.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.924-1502C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43634424 | ||||||
chr20:43634473
|
T | G | 177 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(174): Show | 184 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(181): Show |
intron_variant | MODIFIER | c.924-1453T>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43634473 | ||||||
chr20:43634475
|
C | A | 1 | a0001c0001t0001g0199 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.924-1451C>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43634475 | ||||||
chr20:43634476
|
A | T | 1 | a0001c0001t0001g0112 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.924-1450A>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43634476 | ||||||
chr20:43634525
|
G | A | 2 | a0001c0006t0001g0016a0002c0009t0001g0020 | 2 | NA18906.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.924-1401G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43634525 | ||||||
chr20:43634528
|
A | G | 2 | a0001c0002t0001g0017a0001c0002t0001g0018 | 2 | HG01884.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.924-1398A>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43634528 | ||||||
chr20:43634698
|
A | G | 1 | a0001c0002t0001g0004 | 2 | HG02723.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.924-1228A>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43634698 | ||||||
chr20:43634811
|
A | G | 1 | a0001c0001t0001g0211 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.924-1115A>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43634811 | ||||||
chr20:43634857
|
C | T | 2 | a0001c0002t0001g0017a0001c0002t0001g0018 | 2 | HG01884.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.924-1069C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43634857 | ||||||
chr20:43634941
|
C | T | 1 | a0001c0002t0001g0079 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.924-985C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43634941 | ||||||
chr20:43634947
|
G | A | 1 | a0001c0002t0001g0082 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.924-979G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43634947 | ||||||
chr20:43634959
|
A | G | 2 | a0001c0006t0001g0016a0002c0009t0001g0020 | 2 | NA18906.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.924-967A>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43634959 | ||||||
chr20:43635026
|
G | A | 5 | a0001c0002t0001g0055a0001c0002t0001g0063a0001c0002t0001g0064others(2): Show | 5 | HG02056.hp2 NA18973.hp2 NA18982.hp2 others(2): Show |
intron_variant | MODIFIER | c.924-900G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43635026 | ||||||
chr20:43635170
|
A | C | 177 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(174): Show | 184 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(181): Show |
intron_variant | MODIFIER | c.924-756A>C | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43635170 | ||||||
chr20:43635187
|
GA | G | 178 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(175): Show | 185 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.924-726delA | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr20 | 43635187 | |||||
chr20:43635232
|
A | G | 177 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(174): Show | 184 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(181): Show |
intron_variant | MODIFIER | c.924-694A>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43635232 | ||||||
chr20:43635287
|
A | G | 177 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(174): Show | 184 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(181): Show |
intron_variant | MODIFIER | c.924-639A>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43635287 | ||||||
chr20:43635353
|
C | T | 2 | a0001c0002t0001g0004a0001c0002t0001g0019 | 3 | HG02723.hp2 HG02976.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.924-573C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43635353 | ||||||
chr20:43635364
|
C | T | 1 | a0001c0002t0001g0085 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.924-562C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43635364 | ||||||
chr20:43635377
|
G | A | 177 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(174): Show | 184 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(181): Show |
intron_variant | MODIFIER | c.924-549G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43635377 | ||||||
chr20:43635389
|
C | T | 3 | a0001c0002t0001g0083a0001c0002t0001g0084a0001c0002t0001g0086 | 3 | HG02886.hp1 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.924-537C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43635389 | ||||||
chr20:43635548
|
C | T | 2 | a0001c0001t0001g0136a0001c0001t0001g0177 | 2 | HG00099.hp1 HG01106.hp1 |
intron_variant | MODIFIER | c.924-378C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43635548 | ||||||
chr20:43635558
|
A | C | 10 | a0001c0001t0001g0003a0001c0001t0001g0134a0001c0001t0001g0144others(7): Show | 12 | HG00642.hp2 HG00741.hp1 HG01070.hp2 others(9): Show |
intron_variant | MODIFIER | c.924-368A>C | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43635558 | ||||||
chr20:43635674
|
C | A | 21 | a0001c0002t0001g0009a0001c0002t0001g0010a0001c0002t0001g0087others(18): Show | 23 | HG01081.hp1 HG02083.hp2 HG02486.hp2 others(20): Show |
intron_variant | MODIFIER | c.924-252C>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43635674 | ||||||
chr20:43635728
|
T | C | 4 | a0001c0003t0001g0002a0001c0003t0001g0021a0001c0003t0001g0022others(1): Show | 6 | HG01361.hp2 HG02615.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.924-198T>C | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43635728 | ||||||
chr20:43635862
|
G | A | 177 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(174): Show | 184 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(181): Show |
intron_variant | MODIFIER | c.924-64G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43635862 | ||||||
chr20:43635873
|
G | A | 2 | a0001c0001t0001g0199a0001c0001t0001g0221 | 2 | NA18966.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.924-53G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43635873 | ||||||
chr20:43636086
|
T | C | 177 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(174): Show | 184 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(181): Show |
intron_variant | MODIFIER | c.1011+73T>C | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 11/13 | chr20 | 43636086 | ||||||
chr20:43636367
|
C | T | 6 | a0001c0001t0001g0128a0001c0001t0001g0164a0001c0001t0001g0168others(3): Show | 6 | HG00280.hp1 HG01069.hp2 HG01175.hp2 others(3): Show |
intron_variant | MODIFIER | c.1011+354C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 11/13 | chr20 | 43636367 | ||||||
chr20:43636401
|
T | C | 1 | a0001c0001t0001g0258 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1011+388T>C | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 11/13 | chr20 | 43636401 | ||||||
chr20:43636597
|
G | C | 10 | a0001c0001t0001g0003a0001c0001t0001g0134a0001c0001t0001g0144others(7): Show | 12 | HG00642.hp2 HG00741.hp1 HG01070.hp2 others(9): Show |
intron_variant | MODIFIER | c.1012-548G>C | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 11/13 | chr20 | 43636597 | ||||||
chr20:43636802
|
G | A | 3 | a0001c0002t0001g0106a0001c0002t0001g0107a0001c0002t0001g0108 | 3 | HG02602.hp2 HG02615.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.1012-343G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 11/13 | chr20 | 43636802 | ||||||
chr20:43636867
|
T | C | 11 | a0001c0002t0001g0008a0001c0002t0001g0054a0001c0002t0001g0059others(8): Show | 12 | HG00544.hp2 HG02027.hp1 HG02129.hp2 others(9): Show |
intron_variant | MODIFIER | c.1012-278T>C | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 11/13 | chr20 | 43636867 | ||||||
chr20:43637010
|
A | G | 177 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(174): Show | 184 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(181): Show |
intron_variant | MODIFIER | c.1012-135A>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 11/13 | chr20 | 43637010 | ||||||
chr20:43637012
|
G | A | 6 | a0001c0002t0001g0017a0001c0002t0001g0018a0001c0002t0001g0083others(3): Show | 6 | HG01884.hp1 HG02630.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1012-133G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 11/13 | chr20 | 43637012 | ||||||
chr20:43637060
|
T | C | 216 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(213): Show | 228 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.1012-85T>C | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 11/13 | chr20 | 43637060 | ||||||
chr20:43637326
|
G | A | 167 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(164): Show | 174 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.1120+73G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 12/13 | chr20 | 43637326 | ||||||
chr20:43637416
|
C | T | 10 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0274others(7): Show | 10 | HG00741.hp2 HG01167.hp2 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.1120+163C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 12/13 | chr20 | 43637416 | ||||||
chr20:43637501
|
G | A | 3 | a0001c0001t0001g0217a0001c0001t0001g0233a0001c0001t0001g0234 | 3 | HG01123.hp1 HG01261.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.1120+248G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 12/13 | chr20 | 43637501 | ||||||
chr20:43637510
|
G | A | 3 | a0001c0001t0001g0117a0001c0001t0001g0119a0001c0001t0001g0120 | 3 | HG02486.hp1 HG02886.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1120+257G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 12/13 | chr20 | 43637510 | ||||||
chr20:43637545
|
G | A | 1 | a0001c0002t0001g0087 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1120+292G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 12/13 | chr20 | 43637545 | ||||||
chr20:43637706
|
T | C | 3 | a0001c0003t0001g0002a0001c0003t0001g0021a0001c0003t0001g0022 | 5 | HG02615.hp2 HG02922.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.1120+453T>C | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 12/13 | chr20 | 43637706 | ||||||
chr20:43637734
|
T | C | 1 | a0001c0001t0001g0252 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.1120+481T>C | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 12/13 | chr20 | 43637734 | ||||||
chr20:43637738
|
C | T | 1 | a0001c0001t0001g0218 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1120+485C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 12/13 | chr20 | 43637738 | ||||||
chr20:43637938
|
T | C | 5 | a0001c0002t0001g0082a0001c0003t0001g0002a0001c0003t0001g0021others(2): Show | 7 | HG01361.hp2 HG02615.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.1120+685T>C | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 12/13 | chr20 | 43637938 | ||||||
chr20:43638193
|
AT | A | 210 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(207): Show | 222 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(219): Show |
intron_variant | MODIFIER | c.1120+954delT | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr20 | 43638193 | |||||
chr20:43638193
|
ATT | A | 6 | a0001c0001t0001g0128a0001c0001t0001g0164a0001c0001t0001g0168others(3): Show | 6 | HG00280.hp1 HG01069.hp2 HG01175.hp2 others(3): Show |
intron_variant | MODIFIER | c.1120+953_1120+954d others(4): Show |
IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr20 | 43638193 | |||||
chr20:43638230
|
G | A | 3 | a0001c0002t0001g0106a0001c0002t0001g0107a0001c0002t0001g0108 | 3 | HG02602.hp2 HG02615.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.1120+977G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 12/13 | chr20 | 43638230 | ||||||
chr20:43638268
|
G | A | 3 | a0001c0002t0001g0032a0001c0002t0001g0036a0001c0002t0001g0038 | 3 | HG02135.hp1 NA18939.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.1120+1015G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 12/13 | chr20 | 43638268 | ||||||
chr20:43638352
|
G | C | 1 | a0001c0001t0001g0198 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1120+1099G>C | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 12/13 | chr20 | 43638352 | ||||||
chr20:43638399
|
C | T | 2 | a0001c0002t0001g0017a0001c0002t0001g0018 | 2 | HG01884.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.1120+1146C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 12/13 | chr20 | 43638399 | ||||||
chr20:43638694
|
T | C | 3 | a0001c0001t0001g0248a0001c0001t0001g0249a0001c0001t0001g0251 | 3 | HG02258.hp2 HG02572.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1120+1441T>C | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 12/13 | chr20 | 43638694 | ||||||
chr20:43638832
|
A | G | 3 | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0001t0001g0125 | 3 | HG02055.hp1 HG02809.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1120+1579A>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 12/13 | chr20 | 43638832 | ||||||
chr20:43638934
|
A | T | 2 | a0001c0002t0001g0004a0001c0002t0001g0019 | 3 | HG02723.hp2 HG02976.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1120+1681A>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 12/13 | chr20 | 43638934 | ||||||
chr20:43639168
|
A | G | 1 | a0001c0002t0001g0069 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1120+1915A>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 12/13 | chr20 | 43639168 | ||||||
chr20:43639236
|
C | CA | 167 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(164): Show | 175 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.1120+2000dupA | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr20 | 43639236 | |||||
chr20:43639236
|
C | CAA | 15 | a0001c0001t0001g0158a0001c0001t0001g0187a0001c0001t0001g0188others(12): Show | 15 | HG00438.hp1 HG00438.hp2 HG00741.hp2 others(12): Show |
intron_variant | MODIFIER | c.1120+1999_1120+200 others(6): Show |
IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr20 | 43639236 | |||||
chr20:43639265
|
C | A | 3 | a0001c0002t0001g0106a0001c0002t0001g0107a0001c0002t0001g0108 | 3 | HG02602.hp2 HG02615.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.1120+2012C>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 12/13 | chr20 | 43639265 | ||||||
chr20:43639266
|
G | A | 1 | a0001c0002t0001g0026 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1120+2013G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 12/13 | chr20 | 43639266 | ||||||
chr20:43639297
|
A | G | 1 | a0001c0001t0001g0197 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1120+2044A>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 12/13 | chr20 | 43639297 | ||||||
chr20:43639379
|
C | CA | 23 | a0001c0001t0001g0273a0001c0002t0001g0009a0001c0002t0001g0010others(20): Show | 25 | HG01081.hp1 HG01243.hp1 HG02083.hp2 others(22): Show |
intron_variant | MODIFIER | c.1120+2135dupA | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr20 | 43639379 | |||||
chr20:43639390
|
G | C | 167 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(164): Show | 174 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.1120+2137G>C | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 12/13 | chr20 | 43639390 | ||||||
chr20:43639408
|
C | A | 1 | a0002c0009t0001g0020 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1120+2155C>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 12/13 | chr20 | 43639408 | ||||||
chr20:43639421
|
G | A | 6 | a0001c0002t0001g0093a0001c0002t0001g0097a0001c0002t0001g0098others(3): Show | 6 | NA18952.hp1 NA18972.hp1 NA19000.hp2 others(3): Show |
intron_variant | MODIFIER | c.1120+2168G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 12/13 | chr20 | 43639421 | ||||||
chr20:43639539
|
G | A | 17 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0024others(14): Show | 19 | HG01109.hp2 HG02056.hp1 HG02135.hp1 others(16): Show |
intron_variant | MODIFIER | c.1120+2286G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 12/13 | chr20 | 43639539 | ||||||
chr20:43639584
|
C | T | 3 | a0001c0002t0001g0106a0001c0002t0001g0107a0001c0002t0001g0108 | 3 | HG02602.hp2 HG02615.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.1120+2331C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 12/13 | chr20 | 43639584 | ||||||
chr20:43639618
|
C | T | 1 | a0001c0002t0001g0064 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1120+2365C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 12/13 | chr20 | 43639618 | ||||||
chr20:43639680
|
A | T | 1 | a0001c0002t0001g0075 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1120+2427A>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 12/13 | chr20 | 43639680 | ||||||
chr20:43639681
|
T | A | 1 | a0001c0001t0001g0180 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1120+2428T>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 12/13 | chr20 | 43639681 | ||||||
chr20:43639701
|
C | T | 180 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(177): Show | 187 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.1120+2448C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 12/13 | chr20 | 43639701 | ||||||
chr20:43639763
|
C | T | 1 | a0001c0002t0001g0087 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1120+2510C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 12/13 | chr20 | 43639763 | ||||||
chr20:43639796
|
C | T | 1 | a0001c0002t0001g0010 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1120+2543C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 12/13 | chr20 | 43639796 | ||||||
chr20:43639968
|
C | T | 177 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(174): Show | 184 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(181): Show |
intron_variant | MODIFIER | c.1121-2511C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 12/13 | chr20 | 43639968 | ||||||
chr20:43640181
|
G | A | 4 | a0001c0003t0001g0002a0001c0003t0001g0021a0001c0003t0001g0022others(1): Show | 6 | HG01361.hp2 HG02615.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1121-2298G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 12/13 | chr20 | 43640181 | ||||||
chr20:43640222
|
C | T | 1 | a0001c0001t0001g0158 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1121-2257C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 12/13 | chr20 | 43640222 | ||||||
chr20:43640232
|
G | A | 5 | a0001c0002t0001g0008a0001c0002t0001g0054a0001c0002t0001g0059others(2): Show | 6 | NA18941.hp1 NA18945.hp2 NA18952.hp2 others(3): Show |
intron_variant | MODIFIER | c.1121-2247G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 12/13 | chr20 | 43640232 | ||||||
chr20:43640423
|
G | C | 1 | a0001c0002t0001g0082 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1121-2056G>C | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 12/13 | chr20 | 43640423 | ||||||
chr20:43641030
|
C | CA | 6 | a0001c0002t0001g0039a0001c0002t0001g0042a0001c0002t0001g0052others(3): Show | 6 | HG01175.hp1 HG02257.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.1121-1425dupA | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr20 | 43641030 | |||||
chr20:43641030
|
CA | C | 31 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0017others(28): Show | 35 | HG01109.hp2 HG01361.hp2 HG01884.hp1 others(32): Show |
intron_variant | MODIFIER | c.1121-1425delA | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr20 | 43641030 | |||||
chr20:43641030
|
CAA | C | 21 | a0001c0002t0001g0004a0001c0002t0001g0009a0001c0002t0001g0010others(18): Show | 24 | HG01081.hp1 HG02083.hp2 HG02486.hp2 others(21): Show |
intron_variant | MODIFIER | c.1121-1426_1121-142 others(6): Show |
IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr20 | 43641030 | |||||
chr20:43641030
|
CAAAA | C | 7 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0119others(4): Show | 7 | HG02071.hp1 HG02109.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1121-1428_1121-142 others(8): Show |
IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr20 | 43641030 | |||||
chr20:43641030
|
CAAAAA | C | 165 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(162): Show | 172 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(169): Show |
intron_variant | MODIFIER | c.1121-1429_1121-142 others(9): Show |
IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr20 | 43641030 | |||||
chr20:43641104
|
A | G | 177 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(174): Show | 184 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(181): Show |
intron_variant | MODIFIER | c.1121-1375A>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 12/13 | chr20 | 43641104 | ||||||
chr20:43641112
|
T | A | 1 | a0002c0009t0001g0020 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1121-1367T>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 12/13 | chr20 | 43641112 | ||||||
chr20:43641183
|
T | C | 1 | a0001c0002t0001g0055 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1121-1296T>C | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 12/13 | chr20 | 43641183 | ||||||
chr20:43641218
|
T | G | 216 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(213): Show | 228 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.1121-1261T>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 12/13 | chr20 | 43641218 | ||||||
chr20:43641640
|
C | T | 1 | a0001c0001t0001g0150 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1121-839C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 12/13 | chr20 | 43641640 | ||||||
chr20:43641694
|
C | T | 36 | a0001c0002t0001g0004a0001c0002t0001g0009a0001c0002t0001g0010others(33): Show | 41 | HG01081.hp1 HG01361.hp2 HG01884.hp1 others(38): Show |
intron_variant | MODIFIER | c.1121-785C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 12/13 | chr20 | 43641694 | ||||||
chr20:43641722
|
C | T | 4 | a0001c0003t0001g0002a0001c0003t0001g0021a0001c0003t0001g0022others(1): Show | 6 | HG01361.hp2 HG02615.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1121-757C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 12/13 | chr20 | 43641722 | ||||||
chr20:43641773
|
C | T | 1 | a0001c0001t0001g0277 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1121-706C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 12/13 | chr20 | 43641773 | ||||||
chr20:43642023
|
A | T | 21 | a0001c0002t0001g0009a0001c0002t0001g0010a0001c0002t0001g0087others(18): Show | 23 | HG01081.hp1 HG02083.hp2 HG02486.hp2 others(20): Show |
intron_variant | MODIFIER | c.1121-456A>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 12/13 | chr20 | 43642023 | ||||||
chr20:43642197
|
C | T | 177 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(174): Show | 184 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(181): Show |
intron_variant | MODIFIER | c.1121-282C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 12/13 | chr20 | 43642197 | ||||||
chr20:43642281
|
T | C | 167 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(164): Show | 174 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.1121-198T>C | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 12/13 | chr20 | 43642281 | ||||||
chr20:43642680
|
C | T | 2 | a0001c0002t0001g0065a0001c0002t0001g0070 | 2 | HG02027.hp1 HG02129.hp2 |
intron_variant | MODIFIER | c.1266+56C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43642680 | ||||||
chr20:43642708
|
C | T | 1 | a0001c0002t0001g0077 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1266+84C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43642708 | ||||||
chr20:43642734
|
T | G | 178 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(175): Show | 185 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.1266+110T>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43642734 | ||||||
chr20:43642800
|
G | T | 2 | a0001c0002t0001g0040a0001c0002t0001g0041 | 2 | HG02258.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1266+176G>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43642800 | ||||||
chr20:43642918
|
A | G | 12 | a0001c0001t0001g0116a0001c0001t0001g0227a0001c0002t0001g0092others(9): Show | 12 | NA18952.hp1 NA18959.hp2 NA18963.hp2 others(9): Show |
intron_variant | MODIFIER | c.1266+294A>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43642918 | ||||||
chr20:43642930
|
G | A | 2 | a0001c0001t0001g0116a0001c0001t0001g0227 | 2 | NA18959.hp2 NA18963.hp2 |
intron_variant | MODIFIER | c.1266+306G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43642930 | ||||||
chr20:43642932
|
T | C | 2 | a0001c0001t0001g0116a0001c0001t0001g0227 | 2 | NA18959.hp2 NA18963.hp2 |
intron_variant | MODIFIER | c.1266+308T>C | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43642932 | ||||||
chr20:43642936
|
G | A | 14 | a0001c0002t0001g0010a0001c0002t0001g0092a0001c0002t0001g0093others(11): Show | 15 | HG02083.hp2 HG03491.hp2 HG03492.hp1 others(12): Show |
intron_variant | MODIFIER | c.1266+312G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43642936 | ||||||
chr20:43642936
|
G | T | 2 | a0001c0001t0001g0116a0001c0001t0001g0227 | 2 | NA18959.hp2 NA18963.hp2 |
intron_variant | MODIFIER | c.1266+312G>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43642936 | ||||||
chr20:43642938
|
A | G | 2 | a0001c0001t0001g0116a0001c0001t0001g0227 | 2 | NA18959.hp2 NA18963.hp2 |
intron_variant | MODIFIER | c.1266+314A>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43642938 | ||||||
chr20:43642941
|
C | T | 2 | a0001c0001t0001g0116a0001c0001t0001g0227 | 2 | NA18959.hp2 NA18963.hp2 |
intron_variant | MODIFIER | c.1266+317C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43642941 | ||||||
chr20:43642942
|
A | G | 2 | a0001c0001t0001g0116a0001c0001t0001g0227 | 2 | NA18959.hp2 NA18963.hp2 |
intron_variant | MODIFIER | c.1266+318A>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43642942 | ||||||
chr20:43642955
|
T | G | 2 | a0001c0001t0001g0116a0001c0001t0001g0227 | 2 | NA18959.hp2 NA18963.hp2 |
intron_variant | MODIFIER | c.1266+331T>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43642955 | ||||||
chr20:43642962
|
T | A | 2 | a0001c0001t0001g0116a0001c0001t0001g0227 | 2 | NA18959.hp2 NA18963.hp2 |
intron_variant | MODIFIER | c.1266+338T>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43642962 | ||||||
chr20:43642972
|
G | T | 2 | a0001c0001t0001g0116a0001c0001t0001g0227 | 2 | NA18959.hp2 NA18963.hp2 |
intron_variant | MODIFIER | c.1266+348G>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43642972 | ||||||
chr20:43643037
|
C | T | 1 | a0001c0002t0001g0087 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1266+413C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43643037 | ||||||
chr20:43643119
|
A | G | 1 | a0001c0002t0001g0077 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1266+495A>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43643119 | ||||||
chr20:43643164
|
C | CA | 160 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(157): Show | 170 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(167): Show |
intron_variant | MODIFIER | c.1266+549dupA | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr20 | 43643164 | |||||
chr20:43643164
|
C | CAA | 7 | a0001c0001t0001g0151a0001c0001t0001g0180a0001c0001t0001g0209others(4): Show | 7 | HG01192.hp1 HG02109.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.1266+548_1266+549d others(4): Show |
IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr20 | 43643164 | |||||
chr20:43643174
|
C | A | 1 | a0001c0001t0001g0136 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1266+550C>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43643174 | ||||||
chr20:43643177
|
AAAAAC | A | 4 | a0001c0002t0001g0044a0001c0002t0001g0050a0001c0002t0001g0052others(1): Show | 4 | HG01099.hp1 HG01175.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.1266+568_1266+572d others(7): Show |
IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr20 | 43643177 | |||||
chr20:43643192
|
C | CA | 6 | a0001c0001t0001g0114a0001c0001t0001g0209a0001c0002t0001g0035others(3): Show | 6 | HG01109.hp1 HG02056.hp2 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.1266+578dupA | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr20 | 43643192 | |||||
chr20:43643197
|
A | C | 1 | a0001c0002t0001g0027 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1266+573A>C | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43643197 | ||||||
chr20:43643224
|
ACCTGTAA others(2717): Show |
A | 176 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(173): Show | 183 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(180): Show |
intron_variant | MODIFIER | c.1266+636_1267-953d others(2): Show |
IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr20 | 43643224 | |||||
chr20:43643243
|
TGGGAGGC others(2718): Show |
T | 1 | a0001c0001t0002g0170 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.1266+622_1267-966d others(2): Show |
IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr20 | 43643243 | |||||
chr20:43643509
|
C | T | 3 | a0001c0002t0001g0106a0001c0002t0001g0107a0001c0002t0001g0108 | 3 | HG02602.hp2 HG02615.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.1266+885C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43643509 | ||||||
chr20:43644101
|
T | C | 56 | a0001c0002t0001g0004a0001c0002t0001g0005a0001c0002t0001g0006others(53): Show | 63 | HG01081.hp1 HG01109.hp2 HG01361.hp2 others(60): Show |
intron_variant | MODIFIER | c.1266+1477T>C | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43644101 | ||||||
chr20:43644102
|
G | A | 27 | a0001c0002t0001g0009a0001c0002t0001g0010a0001c0002t0001g0017others(24): Show | 29 | HG01081.hp1 HG01884.hp1 HG02083.hp2 others(26): Show |
intron_variant | MODIFIER | c.1266+1478G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43644102 | ||||||
chr20:43644186
|
A | ATTCCTTG others(2): Show |
39 | a0001c0002t0001g0004a0001c0002t0001g0009a0001c0002t0001g0010others(36): Show | 44 | HG01081.hp1 HG01361.hp2 HG01884.hp1 others(41): Show |
intron_variant | MODIFIER | c.1266+1562_1266+156 others(13): Show |
IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43644186 | ||||||
chr20:43644202
|
G | A | 1 | a0001c0002t0001g0070 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1266+1578G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43644202 | ||||||
chr20:43644294
|
G | T | 1 | a0001c0002t0001g0019 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1266+1670G>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43644294 | ||||||
chr20:43644306
|
T | C | 1 | a0001c0002t0001g0019 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1266+1682T>C | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43644306 | ||||||
chr20:43644309
|
A | T | 1 | a0001c0002t0001g0019 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1266+1685A>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43644309 | ||||||
chr20:43644311
|
T | G | 1 | a0001c0002t0001g0019 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1266+1687T>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43644311 | ||||||
chr20:43644312
|
G | A | 1 | a0001c0002t0001g0019 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1266+1688G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43644312 | ||||||
chr20:43644313
|
T | A | 1 | a0001c0002t0001g0019 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1266+1689T>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43644313 | ||||||
chr20:43644321
|
G | T | 1 | a0001c0002t0001g0019 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1266+1697G>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43644321 | ||||||
chr20:43644325
|
A | T | 1 | a0001c0002t0001g0019 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1266+1701A>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43644325 | ||||||
chr20:43644327
|
C | T | 1 | a0001c0002t0001g0019 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1266+1703C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43644327 | ||||||
chr20:43644328
|
C | A | 1 | a0001c0002t0001g0019 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1266+1704C>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43644328 | ||||||
chr20:43644330
|
T | A | 1 | a0001c0002t0001g0019 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1266+1706T>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43644330 | ||||||
chr20:43644333
|
T | A | 1 | a0001c0002t0001g0019 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1266+1709T>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43644333 | ||||||
chr20:43644334
|
A | G | 1 | a0001c0002t0001g0019 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1266+1710A>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43644334 | ||||||
chr20:43644335
|
A | G | 1 | a0001c0002t0001g0019 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1266+1711A>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43644335 | ||||||
chr20:43644337
|
C | A | 1 | a0001c0002t0001g0019 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1266+1713C>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43644337 | ||||||
chr20:43644342
|
G | C | 1 | a0001c0002t0001g0019 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1266+1718G>C | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43644342 | ||||||
chr20:43644343
|
A | T | 1 | a0001c0002t0001g0019 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1266+1719A>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43644343 | ||||||
chr20:43644348
|
G | C | 1 | a0001c0002t0001g0019 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1266+1724G>C | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43644348 | ||||||
chr20:43644350
|
T | G | 1 | a0001c0002t0001g0019 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1266+1726T>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43644350 | ||||||
chr20:43644355
|
T | G | 1 | a0001c0002t0001g0019 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1266+1731T>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43644355 | ||||||
chr20:43644357
|
A | G | 1 | a0001c0002t0001g0019 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1266+1733A>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43644357 | ||||||
chr20:43644359
|
A | C | 1 | a0001c0002t0001g0019 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1266+1735A>C | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43644359 | ||||||
chr20:43644362
|
A | T | 1 | a0001c0002t0001g0019 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1266+1738A>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43644362 | ||||||
chr20:43644363
|
T | C | 1 | a0001c0002t0001g0019 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1266+1739T>C | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43644363 | ||||||
chr20:43644366
|
G | T | 1 | a0001c0002t0001g0019 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1266+1742G>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43644366 | ||||||
chr20:43644371
|
A | T | 1 | a0001c0002t0001g0019 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1266+1747A>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43644371 | ||||||
chr20:43644372
|
C | T | 3 | a0001c0002t0001g0106a0001c0002t0001g0107a0001c0002t0001g0108 | 3 | HG02602.hp2 HG02615.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.1266+1748C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43644372 | ||||||
chr20:43644375
|
A | G | 1 | a0001c0002t0001g0019 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1266+1751A>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43644375 | ||||||
chr20:43644377
|
A | T | 1 | a0001c0002t0001g0019 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1266+1753A>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43644377 | ||||||
chr20:43644378
|
G | T | 1 | a0001c0002t0001g0019 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1266+1754G>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43644378 | ||||||
chr20:43644383
|
A | G | 1 | a0001c0002t0001g0019 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1266+1759A>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43644383 | ||||||
chr20:43644386
|
A | T | 1 | a0001c0002t0001g0019 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1266+1762A>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43644386 | ||||||
chr20:43644388
|
C | T | 1 | a0001c0002t0001g0019 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1266+1764C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43644388 | ||||||
chr20:43644390
|
A | C | 1 | a0001c0002t0001g0019 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1266+1766A>C | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43644390 | ||||||
chr20:43644391
|
G | T | 1 | a0001c0002t0001g0019 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1266+1767G>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43644391 | ||||||
chr20:43644392
|
G | T | 1 | a0001c0002t0001g0019 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1266+1768G>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43644392 | ||||||
chr20:43644393
|
A | G | 1 | a0001c0002t0001g0019 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1266+1769A>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43644393 | ||||||
chr20:43644395
|
T | G | 1 | a0001c0002t0001g0019 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1266+1771T>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43644395 | ||||||
chr20:43644400
|
G | A | 1 | a0001c0002t0001g0019 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1266+1776G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43644400 | ||||||
chr20:43644402
|
G | A | 1 | a0001c0002t0001g0019 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1266+1778G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43644402 | ||||||
chr20:43644408
|
T | C | 1 | a0001c0002t0001g0019 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1266+1784T>C | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43644408 | ||||||
chr20:43644412
|
T | A | 1 | a0001c0002t0001g0019 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1266+1788T>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43644412 | ||||||
chr20:43644419
|
A | C | 1 | a0001c0002t0001g0019 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1266+1795A>C | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43644419 | ||||||
chr20:43644421
|
G | A | 1 | a0001c0002t0001g0019 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1266+1797G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43644421 | ||||||
chr20:43644423
|
A | T | 1 | a0001c0002t0001g0019 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1266+1799A>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43644423 | ||||||
chr20:43644436
|
A | G | 1 | a0001c0002t0001g0019 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1266+1812A>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43644436 | ||||||
chr20:43644440
|
G | A | 1 | a0001c0002t0001g0019 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1266+1816G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43644440 | ||||||
chr20:43644442
|
A | C | 1 | a0001c0002t0001g0019 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1266+1818A>C | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43644442 | ||||||
chr20:43644451
|
A | G | 1 | a0001c0002t0001g0019 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1266+1827A>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43644451 | ||||||
chr20:43644452
|
G | T | 1 | a0001c0002t0001g0019 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1266+1828G>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43644452 | ||||||
chr20:43644454
|
A | C | 1 | a0001c0002t0001g0019 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1266+1830A>C | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43644454 | ||||||
chr20:43644459
|
A | C | 1 | a0001c0002t0001g0019 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1266+1835A>C | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43644459 | ||||||
chr20:43644460
|
G | T | 1 | a0001c0002t0001g0019 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1266+1836G>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43644460 | ||||||
chr20:43644462
|
G | C | 1 | a0001c0002t0001g0019 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1266+1838G>C | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43644462 | ||||||
chr20:43644464
|
A | T | 1 | a0001c0002t0001g0019 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1266+1840A>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43644464 | ||||||
chr20:43644465
|
C | A | 1 | a0001c0002t0001g0019 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1266+1841C>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43644465 | ||||||
chr20:43644466
|
A | G | 1 | a0001c0002t0001g0019 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1266+1842A>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43644466 | ||||||
chr20:43644470
|
A | T | 1 | a0001c0002t0001g0019 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1266+1846A>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43644470 | ||||||
chr20:43644472
|
A | T | 1 | a0001c0002t0001g0019 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1266+1848A>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43644472 | ||||||
chr20:43644473
|
A | G | 1 | a0001c0002t0001g0019 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1266+1849A>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43644473 | ||||||
chr20:43644474
|
G | C | 1 | a0001c0002t0001g0019 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1266+1850G>C | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43644474 | ||||||
chr20:43644477
|
A | T | 1 | a0001c0002t0001g0019 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1266+1853A>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43644477 | ||||||
chr20:43644478
|
A | T | 1 | a0001c0002t0001g0019 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1266+1854A>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43644478 | ||||||
chr20:43644479
|
A | T | 1 | a0001c0002t0001g0019 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1266+1855A>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43644479 | ||||||
chr20:43644480
|
A | C | 1 | a0001c0002t0001g0019 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1266+1856A>C | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43644480 | ||||||
chr20:43644482
|
A | T | 1 | a0001c0002t0001g0019 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1266+1858A>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43644482 | ||||||
chr20:43644491
|
A | G | 1 | a0001c0002t0001g0019 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1266+1867A>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43644491 | ||||||
chr20:43644492
|
A | T | 1 | a0001c0002t0001g0019 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1266+1868A>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43644492 | ||||||
chr20:43644649
|
G | A | 1 | a0001c0002t0001g0024 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1266+2025G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43644649 | ||||||
chr20:43644705
|
G | A | 3 | a0001c0002t0001g0089a0001c0002t0001g0091a0001c0002t0001g0105 | 3 | HG01081.hp1 HG02647.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1266+2081G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43644705 | ||||||
chr20:43644730
|
A | G | 39 | a0001c0002t0001g0004a0001c0002t0001g0009a0001c0002t0001g0010others(36): Show | 44 | HG01081.hp1 HG01361.hp2 HG01884.hp1 others(41): Show |
intron_variant | MODIFIER | c.1266+2106A>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43644730 | ||||||
chr20:43645137
|
G | A | 2 | a0001c0002t0001g0017a0001c0002t0001g0018 | 2 | HG01884.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.1267-1799G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43645137 | ||||||
chr20:43645385
|
G | A | 1 | a0001c0002t0001g0082 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1267-1551G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43645385 | ||||||
chr20:43645401
|
C | T | 21 | a0001c0002t0001g0009a0001c0002t0001g0010a0001c0002t0001g0087others(18): Show | 23 | HG01081.hp1 HG02083.hp2 HG02486.hp2 others(20): Show |
intron_variant | MODIFIER | c.1267-1535C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43645401 | ||||||
chr20:43645733
|
G | A | 4 | a0001c0003t0001g0002a0001c0003t0001g0021a0001c0003t0001g0022others(1): Show | 6 | HG01361.hp2 HG02615.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1267-1203G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43645733 | ||||||
chr20:43645820
|
A | G | 39 | a0001c0002t0001g0004a0001c0002t0001g0009a0001c0002t0001g0010others(36): Show | 44 | HG01081.hp1 HG01361.hp2 HG01884.hp1 others(41): Show |
intron_variant | MODIFIER | c.1267-1116A>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43645820 | ||||||
chr20:43645864
|
A | T | 37 | a0001c0002t0001g0004a0001c0002t0001g0009a0001c0002t0001g0017others(34): Show | 41 | HG01081.hp1 HG01361.hp2 HG01884.hp1 others(38): Show |
intron_variant | MODIFIER | c.1267-1072A>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43645864 | ||||||
chr20:43645865
|
A | T | 2 | a0001c0002t0001g0010a0001c0002t0001g0094 | 3 | HG03491.hp2 HG03492.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.1267-1071A>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43645865 | ||||||
chr20:43645975
|
C | T | 2 | a0001c0002t0001g0017a0001c0002t0001g0018 | 2 | HG01884.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.1267-961C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43645975 | ||||||
chr20:43646067
|
C | T | 1 | a0001c0002t0001g0019 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1267-869C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43646067 | ||||||
chr20:43646068
|
G | A | 1 | a0001c0001t0001g0200 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1267-868G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43646068 | ||||||
chr20:43646069
|
C | T | 29 | a0001c0001t0001g0012a0001c0001t0001g0111a0001c0001t0001g0112others(26): Show | 30 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(27): Show |
intron_variant | MODIFIER | c.1267-867C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43646069 | ||||||
chr20:43646168
|
G | A | 1 | a0001c0002t0001g0042 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1267-768G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43646168 | ||||||
chr20:43646209
|
C | CA | 16 | a0001c0002t0001g0010a0001c0002t0001g0033a0001c0002t0001g0041others(13): Show | 17 | HG02056.hp1 HG02083.hp2 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.1267-711dupA | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr20 | 43646209 | |||||
chr20:43646209
|
C | CAA | 8 | a0001c0002t0001g0009a0001c0002t0001g0087a0001c0002t0001g0088others(5): Show | 9 | HG01081.hp1 HG02486.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.1267-712_1267-711d others(4): Show |
IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr20 | 43646209 | |||||
chr20:43646209
|
CA | C | 173 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(170): Show | 180 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(177): Show |
intron_variant | MODIFIER | c.1267-711delA | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr20 | 43646209 | |||||
chr20:43646336
|
A | T | 1 | a0001c0001t0001g0164 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1267-600A>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43646336 | ||||||
chr20:43646508
|
T | C | 4 | a0001c0001t0001g0229a0001c0001t0001g0230a0001c0001t0001g0231others(1): Show | 4 | HG01884.hp2 HG02145.hp1 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.1267-428T>C | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43646508 | ||||||
chr20:43646528
|
G | A | 3 | a0001c0002t0001g0106a0001c0002t0001g0107a0001c0002t0001g0108 | 3 | HG02602.hp2 HG02615.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.1267-408G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43646528 | ||||||
chr20:43646772
|
A | G | 2 | a0001c0001t0001g0128a0001c0001t0001g0179 | 2 | HG02300.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.1267-164A>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43646772 | ||||||
chr20:43646812
|
A | G | 1 | a0001c0002t0001g0049 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1267-124A>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43646812 | ||||||
chr20:43646859
|
G | T | 233 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(230): Show | 247 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.1267-77G>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43646859 |