geneid | 57560 |
---|---|
ensemblid | ENSG00000068885.15 |
hgncid | 29262 |
symbol | IFT80 |
name | intraflagellar transport 80 |
refseq_nuc | NM_020800.3 |
refseq_prot | NP_065851.1 |
ensembl_nuc | ENST00000326448.12 |
ensembl_prot | ENSP00000312778.7 |
mane_status | MANE Select |
chr | chr3 |
start | 160256986 |
end | 160399225 |
strand | - |
ver | v1.2 |
region | chr3:160256986-160399225 |
region5000 | chr3:160251986-160404225 |
regionname0 | IFT80_chr3_160256986_160399225 |
regionname5000 | IFT80_chr3_160251986_160404225 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 777 | 120 | 37 | 25 | 30 | 8 | 18 | 23 | IFT80_chr3_160251986_160404225 | IFT80 | copy fasta | chr3 | 160251986 | 160404225 |
a0002 | 0/0 | 777 | 88 | 51 | 14 | 11 | 4 | 8 | 9 | IFT80_chr3_160251986_160404225 | IFT80 | copy fasta | chr3 | 160251986 | 160404225 |
a0003 | 0/0 | 777 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | copy fasta | chr3 | 160251986 | 160404225 |
a0004 | 0/0 | 777 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | copy fasta | chr3 | 160251986 | 160404225 |
a0005 | 0/0 | 777 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | copy fasta | chr3 | 160251986 | 160404225 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 2334 | 119 | 37 | 24 | 30 | 8 | 18 | IFT80_chr3_160251986_160404225 | IFT80 | copy fasta | chr3 | 160251986 | 160404225 |
c0002 | 0/0 | 2334 | 78 | 44 | 11 | 11 | 4 | 8 | IFT80_chr3_160251986_160404225 | IFT80 | copy fasta | chr3 | 160251986 | 160404225 |
c0003 | 0/0 | 2334 | 9 | 6 | 3 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | copy fasta | chr3 | 160251986 | 160404225 |
c0004 | 0/0 | 2334 | 2 | 1 | 1 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | copy fasta | chr3 | 160251986 | 160404225 |
c0005 | 0/0 | 2334 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | copy fasta | chr3 | 160251986 | 160404225 |
c0006 | 0/0 | 2334 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | copy fasta | chr3 | 160251986 | 160404225 |
c0007 | 0/0 | 2334 | 1 | 0 | 0 | 1 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | copy fasta | chr3 | 160251986 | 160404225 |
c0008 | 0/0 | 2334 | 1 | 0 | 1 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | copy fasta | chr3 | 160251986 | 160404225 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 1666 | 145 | 40 | 32 | 35 | 12 | 24 | IFT80_chr3_160251986_160404225 | IFT80 | copy fasta | chr3 | 160251986 | 160404225 |
t0002 | 0/0 | 1666 | 45 | 36 | 8 | 0 | 0 | 1 | IFT80_chr3_160251986_160404225 | IFT80 | copy fasta | chr3 | 160251986 | 160404225 |
t0003 | 0/0 | 1666 | 9 | 9 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | copy fasta | chr3 | 160251986 | 160404225 |
t0004 | 0/0 | 1666 | 5 | 0 | 0 | 5 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | copy fasta | chr3 | 160251986 | 160404225 |
t0005 | 0/0 | 1666 | 2 | 2 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | copy fasta | chr3 | 160251986 | 160404225 |
t0006 | 0/0 | 1666 | 2 | 0 | 0 | 2 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | copy fasta | chr3 | 160251986 | 160404225 |
t0007 | 0/0 | 1666 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | copy fasta | chr3 | 160251986 | 160404225 |
t0008 | 0/0 | 1666 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | copy fasta | chr3 | 160251986 | 160404225 |
t0009 | 0/0 | 1666 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | copy fasta | chr3 | 160251986 | 160404225 |
t0010 | 0/0 | 1666 | 1 | 0 | 0 | 0 | 0 | 1 | IFT80_chr3_160251986_160404225 | IFT80 | copy fasta | chr3 | 160251986 | 160404225 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
g0009 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
g0074 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
g0109 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
g0144 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
g0155 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
g0174 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 2334 | 119 | 37 | 24 | 30 | 8 | 18 | IFT80_chr3_160251986_160404225 | IFT80 | copy fasta | chr3 | 160251986 | 160404225 |
a0001c0008 | 0/0 | 2334 | 1 | 0 | 1 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | copy fasta | chr3 | 160251986 | 160404225 |
a0002c0002 | 0/0 | 2334 | 78 | 44 | 11 | 11 | 4 | 8 | IFT80_chr3_160251986_160404225 | IFT80 | copy fasta | chr3 | 160251986 | 160404225 |
a0002c0003 | 0/0 | 2334 | 9 | 6 | 3 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | copy fasta | chr3 | 160251986 | 160404225 |
a0002c0006 | 0/0 | 2334 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | copy fasta | chr3 | 160251986 | 160404225 |
a0003c0004 | 0/0 | 2334 | 2 | 1 | 1 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | copy fasta | chr3 | 160251986 | 160404225 |
a0004c0005 | 0/0 | 2334 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | copy fasta | chr3 | 160251986 | 160404225 |
a0005c0007 | 0/0 | 2334 | 1 | 0 | 0 | 1 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | copy fasta | chr3 | 160251986 | 160404225 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 3999 | 114 | 35 | 24 | 28 | 8 | 17 | IFT80_chr3_160251986_160404225 | IFT80 | copy fasta | chr3 | 160251986 | 160404225 |
a0001c0001t0005 | 0/0 | 3999 | 2 | 2 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | copy fasta | chr3 | 160251986 | 160404225 |
a0001c0001t0006 | 0/0 | 3999 | 2 | 0 | 0 | 2 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | copy fasta | chr3 | 160251986 | 160404225 |
a0001c0001t0010 | 0/0 | 3999 | 1 | 0 | 0 | 0 | 0 | 1 | IFT80_chr3_160251986_160404225 | IFT80 | copy fasta | chr3 | 160251986 | 160404225 |
a0001c0008t0001 | 0/0 | 3999 | 1 | 0 | 1 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | copy fasta | chr3 | 160251986 | 160404225 |
a0002c0002t0001 | 0/0 | 3999 | 29 | 5 | 7 | 6 | 4 | 7 | IFT80_chr3_160251986_160404225 | IFT80 | copy fasta | chr3 | 160251986 | 160404225 |
a0002c0002t0002 | 0/0 | 3999 | 34 | 29 | 4 | 0 | 0 | 1 | IFT80_chr3_160251986_160404225 | IFT80 | copy fasta | chr3 | 160251986 | 160404225 |
a0002c0002t0003 | 0/0 | 3999 | 9 | 9 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | copy fasta | chr3 | 160251986 | 160404225 |
a0002c0002t0004 | 0/0 | 3999 | 5 | 0 | 0 | 5 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | copy fasta | chr3 | 160251986 | 160404225 |
a0002c0002t0007 | 0/0 | 3999 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | copy fasta | chr3 | 160251986 | 160404225 |
a0002c0003t0002 | 0/0 | 3999 | 8 | 5 | 3 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | copy fasta | chr3 | 160251986 | 160404225 |
a0002c0003t0008 | 0/0 | 3999 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | copy fasta | chr3 | 160251986 | 160404225 |
a0002c0006t0002 | 0/0 | 3999 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | copy fasta | chr3 | 160251986 | 160404225 |
a0003c0004t0002 | 0/0 | 3999 | 2 | 1 | 1 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | copy fasta | chr3 | 160251986 | 160404225 |
a0004c0005t0009 | 0/0 | 3999 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | copy fasta | chr3 | 160251986 | 160404225 |
a0005c0007t0001 | 0/0 | 3999 | 1 | 0 | 0 | 1 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | copy fasta | chr3 | 160251986 | 160404225 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0009 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0144 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0155 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0005g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0005g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0006g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0006g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0010g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0008t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0002c0002t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0002c0002t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0002c0002t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0002c0002t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0002c0002t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0002c0002t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0002c0002t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0002c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0002c0002t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0002c0002t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0002c0002t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0002c0002t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0002c0002t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0002c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0002c0002t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0002c0002t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0002c0002t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0002c0002t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0002c0002t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0002c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0002c0002t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0002c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0002c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0002c0002t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0002c0002t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0002c0002t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0002c0002t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0002c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0002c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0002c0002t0002g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0002c0002t0002g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0002c0002t0002g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0002c0002t0002g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0002c0002t0002g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0002c0002t0002g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0002c0002t0002g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0002c0002t0002g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0002c0002t0002g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0002c0002t0002g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0002c0002t0002g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0002c0002t0002g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0002c0002t0002g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0002c0002t0002g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0002c0002t0002g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0002c0002t0002g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0002c0002t0002g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0002c0002t0002g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0002c0002t0002g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0002c0002t0002g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0002c0002t0002g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0002c0002t0002g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0002c0002t0002g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0002c0002t0002g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0002c0002t0002g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0002c0002t0002g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0002c0002t0002g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0002c0002t0002g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0002c0002t0002g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0002c0002t0002g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0002c0002t0002g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0002c0002t0002g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0002c0002t0003g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0002c0002t0003g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0002c0002t0003g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0002c0002t0003g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0002c0002t0003g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0002c0002t0003g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0002c0002t0003g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0002c0002t0003g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0002c0002t0004g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0002c0002t0004g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0002c0002t0004g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0002c0002t0004g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0002c0002t0004g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0002c0002t0007g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0002c0003t0002g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0002c0003t0002g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0002c0003t0002g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0002c0003t0002g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0002c0003t0002g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0002c0003t0002g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0002c0003t0002g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0002c0003t0002g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0002c0003t0008g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0002c0006t0002g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0003c0004t0002g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0003c0004t0002g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0004c0005t0009g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0005c0007t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0002 | c0002 | t0001 | g0057 | EUR | GBR | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0009 | EUR | GBR | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG00140 | hp1 | a0002 | c0002 | t0001 | g0075 | EUR | GBR | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0109 | EUR | GBR | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG00280 | hp1 | a0002 | c0002 | t0001 | g0072 | EUR | FIN | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0120 | EUR | FIN | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0147 | EUR | FIN | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0180 | EUR | FIN | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | CHS | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG00423 | hp2 | a0002 | c0002 | t0001 | g0062 | EAS | CHS | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | CHS | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG00558 | hp2 | a0002 | c0002 | t0001 | g0058 | EAS | CHS | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0141 | AMR | PUR | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0168 | AMR | PUR | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG00735 | hp1 | a0002 | c0002 | t0001 | g0070 | AMR | PUR | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0184 | AMR | PUR | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0169 | AMR | PUR | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG00738 | hp2 | a0002 | c0003 | t0002 | g0081 | AMR | PUR | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0115 | AMR | PUR | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG00741 | hp2 | a0002 | c0002 | t0001 | g0071 | AMR | PUR | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0150 | AMR | PUR | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG01069 | hp2 | a0002 | c0002 | t0002 | g0082 | AMR | PUR | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0133 | AMR | PUR | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0199 | AMR | PUR | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0149 | AMR | PUR | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG01106 | hp2 | a0002 | c0002 | t0001 | g0073 | AMR | PUR | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0092 | AMR | PUR | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0170 | AMR | PUR | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG01167 | hp1 | a0002 | c0003 | t0002 | g0080 | AMR | PUR | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG01167 | hp2 | a0002 | c0002 | t0002 | g0157 | AMR | PUR | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG01168 | hp1 | a0002 | c0002 | t0001 | g0069 | AMR | PUR | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0148 | AMR | PUR | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG01169 | hp1 | a0002 | c0002 | t0002 | g0158 | AMR | PUR | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG01169 | hp2 | a0002 | c0002 | t0001 | g0068 | AMR | PUR | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG01243 | hp1 | a0002 | c0002 | t0002 | g0035 | AMR | PUR | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0121 | AMR | PUR | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0154 | AMR | CLM | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG01255 | hp2 | a0003 | c0004 | t0002 | g0026 | AMR | CLM | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG01261 | hp1 | a0002 | c0003 | t0002 | g0079 | AMR | CLM | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0135 | AMR | CLM | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG01358 | hp1 | a0002 | c0002 | t0001 | g0056 | AMR | CLM | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0136 | AMR | CLM | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG01361 | hp2 | a0002 | c0002 | t0001 | g0061 | AMR | CLM | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG01433 | hp1 | a0001 | c0008 | t0001 | g0164 | AMR | CLM | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0171 | AMR | CLM | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0102 | EUR | IBS | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG01516 | hp2 | a0002 | c0002 | t0001 | g0074 | EUR | IBS | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0175 | AFR | ACB | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG01891 | hp2 | a0002 | c0003 | t0002 | g0054 | AFR | ACB | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0189 | AMR | PEL | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0131 | AMR | PEL | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0194 | AMR | PEL | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0118 | AMR | PEL | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG02055 | hp1 | a0002 | c0002 | t0002 | g0021 | AFR | ACB | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0186 | AFR | ACB | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | KHV | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | KHV | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG02257 | hp1 | a0002 | c0002 | t0001 | g0063 | AFR | ACB | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0161 | AFR | ACB | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0098 | AFR | ACB | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG02258 | hp2 | a0002 | c0002 | t0002 | g0204 | AFR | ACB | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0179 | AFR | ACB | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG02280 | hp2 | a0002 | c0002 | t0002 | g0023 | AFR | ACB | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0190 | AMR | PEL | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0129 | AMR | PEL | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG02451 | hp1 | a0002 | c0002 | t0002 | g0025 | AFR | ACB | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG02451 | hp2 | a0002 | c0002 | t0003 | g0030 | AFR | ACB | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG02523 | hp1 | a0005 | c0007 | t0001 | g0137 | EAS | KHV | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | KHV | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG02602 | hp1 | a0002 | c0002 | t0001 | g0085 | SAS | PJL | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0146 | SAS | PJL | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG02615 | hp1 | a0002 | c0002 | t0003 | g0041 | AFR | GWD | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG02615 | hp2 | a0002 | c0002 | t0002 | g0083 | AFR | GWD | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG02622 | hp1 | a0002 | c0002 | t0001 | g0076 | AFR | GWD | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0095 | AFR | GWD | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG02630 | hp1 | a0002 | c0002 | t0002 | g0172 | AFR | GWD | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG02630 | hp2 | a0002 | c0003 | t0002 | g0051 | AFR | GWD | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG02647 | hp1 | a0002 | c0003 | t0002 | g0050 | AFR | GWD | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG02647 | hp2 | a0002 | c0002 | t0002 | g0037 | AFR | GWD | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG02717 | hp1 | a0002 | c0002 | t0002 | g0024 | AFR | GWD | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG02717 | hp2 | a0002 | c0002 | t0002 | g0049 | AFR | GWD | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG02723 | hp1 | a0002 | c0002 | t0002 | g0055 | AFR | GWD | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG02723 | hp2 | a0002 | c0002 | t0001 | g0033 | AFR | GWD | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0151 | SAS | PJL | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0188 | SAS | PJL | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG02809 | hp1 | a0001 | c0001 | t0005 | g0093 | AFR | GWD | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0125 | AFR | GWD | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0145 | AFR | GWD | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG02818 | hp2 | a0002 | c0002 | t0001 | g0078 | AFR | GWD | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG02886 | hp1 | a0002 | c0002 | t0002 | g0003 | AFR | GWD | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG02886 | hp2 | a0002 | c0002 | t0002 | g0028 | AFR | GWD | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG02895 | hp1 | a0001 | c0001 | t0005 | g0126 | AFR | GWD | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG02895 | hp2 | a0002 | c0002 | t0003 | g0002 | AFR | GWD | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0090 | AFR | GWD | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG02897 | hp2 | a0002 | c0002 | t0003 | g0002 | AFR | GWD | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0185 | AFR | ESN | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG02922 | hp2 | a0002 | c0002 | t0003 | g0029 | AFR | ESN | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG02965 | hp1 | a0002 | c0002 | t0002 | g0048 | AFR | ESN | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG02965 | hp2 | a0002 | c0002 | t0002 | g0205 | AFR | ESN | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG02970 | hp1 | a0002 | c0002 | t0003 | g0031 | AFR | ESN | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG02970 | hp2 | a0003 | c0004 | t0002 | g0027 | AFR | ESN | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ESN | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG02976 | hp2 | a0004 | c0005 | t0009 | g0087 | AFR | ESN | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0122 | AFR | GWD | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG03041 | hp2 | a0002 | c0002 | t0007 | g0088 | AFR | GWD | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0162 | AFR | MSL | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG03098 | hp2 | a0002 | c0002 | t0003 | g0039 | AFR | MSL | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | ESN | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG03130 | hp2 | a0002 | c0002 | t0002 | g0203 | AFR | ESN | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG03139 | hp1 | a0002 | c0002 | t0002 | g0032 | AFR | ESN | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0096 | AFR | ESN | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG03195 | hp1 | a0002 | c0006 | t0002 | g0014 | AFR | ESN | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0097 | AFR | ESN | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG03209 | hp1 | a0002 | c0002 | t0002 | g0036 | AFR | MSL | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0124 | AFR | MSL | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG03225 | hp1 | a0002 | c0002 | t0002 | g0004 | AFR | MSL | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG03225 | hp2 | a0002 | c0002 | t0002 | g0003 | AFR | MSL | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0178 | SAS | PJL | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG03239 | hp2 | a0002 | c0002 | t0001 | g0060 | SAS | PJL | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0101 | AFR | MSL | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG03453 | hp2 | a0002 | c0002 | t0002 | g0022 | AFR | MSL | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0116 | SAS | PJL | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG03490 | hp2 | a0002 | c0002 | t0001 | g0084 | SAS | PJL | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG03516 | hp1 | a0002 | c0002 | t0002 | g0202 | AFR | ESN | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0187 | AFR | ESN | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG03540 | hp1 | a0002 | c0003 | t0002 | g0053 | AFR | GWD | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0123 | AFR | GWD | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG03579 | hp1 | a0002 | c0003 | t0008 | g0045 | AFR | MSL | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG03579 | hp2 | a0002 | c0002 | t0001 | g0077 | AFR | MSL | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0113 | SAS | PJL | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0183 | SAS | PJL | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG03710 | hp1 | a0002 | c0002 | t0001 | g0067 | SAS | PJL | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG03710 | hp2 | a0002 | c0002 | t0002 | g0173 | SAS | PJL | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0176 | SAS | BEB | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0143 | SAS | BEB | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | BEB | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0089 | SAS | BEB | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG03942 | hp1 | a0002 | c0002 | t0001 | g0046 | SAS | BEB | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0111 | SAS | BEB | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0104 | SAS | STU | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0013 | SAS | STU | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG04184 | hp1 | a0001 | c0001 | t0010 | g0114 | SAS | BEB | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG04184 | hp2 | a0002 | c0002 | t0001 | g0047 | SAS | BEB | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0139 | SAS | STU | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0182 | SAS | STU | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
NA18522 | hp1 | a0002 | c0003 | t0002 | g0052 | AFR | YRI | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0103 | AFR | YRI | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | CHB | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
NA18747 | hp2 | a0001 | c0001 | t0006 | g0200 | EAS | CHB | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0167 | AFR | YRI | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0100 | AFR | YRI | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
NA18942 | hp1 | a0002 | c0002 | t0001 | g0065 | EAS | JPT | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
NA18951 | hp1 | a0002 | c0002 | t0001 | g0086 | EAS | JPT | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
NA18960 | hp1 | a0002 | c0002 | t0004 | g0042 | EAS | JPT | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
NA18968 | hp1 | a0002 | c0002 | t0001 | g0064 | EAS | JPT | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
NA18983 | hp2 | a0002 | c0002 | t0004 | g0043 | EAS | JPT | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
NA18990 | hp1 | a0002 | c0002 | t0004 | g0019 | EAS | JPT | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
NA19030 | hp1 | a0002 | c0002 | t0002 | g0159 | AFR | LWK | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0153 | AFR | LWK | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
NA19043 | hp1 | a0002 | c0002 | t0002 | g0044 | AFR | LWK | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
NA19043 | hp2 | a0002 | c0002 | t0003 | g0040 | AFR | LWK | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
NA19064 | hp2 | a0002 | c0002 | t0001 | g0059 | EAS | JPT | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
NA19084 | hp2 | a0002 | c0002 | t0004 | g0018 | EAS | JPT | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
NA19087 | hp2 | a0001 | c0001 | t0006 | g0198 | EAS | JPT | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
NA19088 | hp2 | a0002 | c0002 | t0004 | g0020 | EAS | JPT | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0099 | AFR | YRI | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | YRI | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0163 | AFR | ASW | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
NA20129 | hp2 | a0002 | c0002 | t0002 | g0034 | AFR | ASW | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0174 | EUR | TSI | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0127 | EUR | TSI | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
NA20905 | hp1 | a0002 | c0002 | t0001 | g0066 | SAS | GIH | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0112 | SAS | GIH | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0140 | AFR | ACB | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0094 | AFR | ACB | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG02486 | hp1 | a0002 | c0002 | t0002 | g0015 | AFR | ACB | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG02486 | hp2 | a0002 | c0002 | t0003 | g0038 | AFR | ACB | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0165 | AFR | MSL | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG03471 | hp2 | a0002 | c0002 | t0002 | g0004 | AFR | MSL | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | USA | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG06807 | hp2 | a0002 | c0002 | t0002 | g0156 | AFR | USA | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
NA20300 | hp1 | a0002 | c0002 | t0002 | g0160 | AFR | USA | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0117 | AFR | USA | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0166 | AFR | LWK | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
NA21309 | hp2 | a0002 | c0002 | t0002 | g0201 | AFR | LWK | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0144 | REF | REF | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0155 | REF | REF | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:160277643
|
C | T | 1 | a0003 | 2 | HG01255.hp2 HG02970.hp2 |
missense_variant | MODERATE | c.1864G>A | p.Ala622Thr | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 17/20 | 1990/3999 | 1864/2334 | 622/777 | chr3 | 160277643 | ||
chr3:160279273
|
T | A | 3 | a0002a0003a0004 | 91 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(88): Show |
missense_variant | MODERATE | c.1756A>T | p.Thr586Ser | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 16/20 | 1882/3999 | 1756/2334 | 586/777 | chr3 | 160279273 | ||
chr3:160280704
|
C | T | 1 | a0005 | 1 | HG02523.hp1 | missense_variant | MODERATE | c.1627G>A | p.Asp543Asn | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 15/20 | 1753/3999 | 1627/2334 | 543/777 | chr3 | 160280704 | ||
chr3:160307663
|
G | A | 1 | a0005 | 1 | HG02523.hp1 | missense_variant&splice_region_variant | MODERATE | c.1076C>T | p.Ser359Phe | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 10/20 | 1202/3999 | 1076/2334 | 359/777 | chr3 | 160307663 | ||
chr3:160319837
|
C | T | 1 | a0004 | 1 | HG02976.hp2 | missense_variant | MODERATE | c.880G>A | p.Val294Ile | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/20 | 1006/3999 | 880/2334 | 294/777 | chr3 | 160319837 |
chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:160268497
|
A | G | 1 | a0002c0006 | 1 | HG03195.hp1 | synonymous_variant | LOW | c.2139T>C | p.Asp713Asp | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 19/20 | 2265/3999 | 2139/2334 | 713/777 | chr3 | 160268497 | ||
chr3:160366130
|
C | T | 1 | a0002c0003 | 9 | HG00738.hp2 HG01167.hp1 HG01261.hp1 others(6): Show |
synonymous_variant | LOW | c.462G>A | p.Ala154Ala | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 6/20 | 588/3999 | 462/2334 | 154/777 | chr3 | 160366130 | ||
chr3:160381549
|
T | G | 1 | a0001c0008 | 1 | HG01433.hp1 | synonymous_variant | LOW | c.213A>C | p.Val71Val | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 3/20 | 339/3999 | 213/2334 | 71/777 | chr3 | 160381549 |
chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:160257271
|
G | A | 1 | a0004c0005t0009 | 1 | HG02976.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1254C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 20/20 | 1254 | chr3 | 160257271 | |||||
chr3:160257321
|
C | T | 2 | a0002c0002t0004a0004c0005t0009 | 6 | HG02976.hp2 NA18960.hp1 NA18983.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1204G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 20/20 | 1204 | chr3 | 160257321 | |||||
chr3:160257404
|
A | G | 1 | a0001c0001t0010 | 1 | HG04184.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1121T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 20/20 | 1121 | chr3 | 160257404 | |||||
chr3:160257436
|
A | G | 1 | a0002c0003t0008 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1089T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 20/20 | 1089 | chr3 | 160257436 | |||||
chr3:160257848
|
T | C | 1 | a0001c0001t0006 | 2 | NA18747.hp2 NA19087.hp2 |
3_prime_UTR_variant | MODIFIER | c.*677A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 20/20 | 677 | chr3 | 160257848 | |||||
chr3:160258271
|
A | G | 1 | a0002c0002t0007 | 1 | HG03041.hp2 | 3_prime_UTR_variant | MODIFIER | c.*254T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 20/20 | 254 | chr3 | 160258271 | |||||
chr3:160258343
|
A | G | 1 | a0001c0001t0005 | 2 | HG02809.hp1 HG02895.hp1 |
3_prime_UTR_variant | MODIFIER | c.*182T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 20/20 | 182 | chr3 | 160258343 | |||||
chr3:160258483
|
C | T | 9 | a0002c0002t0002a0002c0002t0003a0002c0002t0004others(6): Show | 62 | HG00738.hp2 HG01069.hp2 HG01167.hp1 others(59): Show |
3_prime_UTR_variant | MODIFIER | c.*42G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 20/20 | 42 | chr3 | 160258483 | |||||
chr3:160384640
|
G | A | 1 | a0002c0002t0003 | 9 | HG02451.hp2 HG02486.hp2 HG02615.hp1 others(6): Show |
5_prime_UTR_variant | MODIFIER | c.-40C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 2/20 | 40 | chr3 | 160384640 |
chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:160258644
|
G | GA | 63 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(60): Show | 64 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(61): Show |
intron_variant | MODIFIER | c.2224-10dupT | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 19/19 | chr3 | 160258644 | ||||||
chr3:160258644
|
GA | G | 7 | a0002c0002t0002g0172a0002c0002t0002g0173a0002c0002t0002g0201others(4): Show | 7 | HG02258.hp2 HG02630.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.2224-10delT | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 19/19 | chr3 | 160258644 | ||||||
chr3:160258679
|
A | C | 1 | a0002c0002t0002g0055 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2224-44T>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 19/19 | chr3 | 160258679 | ||||||
chr3:160258945
|
A | G | 8 | a0002c0002t0002g0021a0002c0002t0002g0022a0002c0002t0002g0023others(5): Show | 8 | HG01255.hp2 HG02055.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.2224-310T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 19/19 | chr3 | 160258945 | ||||||
chr3:160259291
|
C | T | 1 | a0001c0001t0001g0095 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2224-656G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 19/19 | chr3 | 160259291 | ||||||
chr3:160259366
|
T | C | 1 | a0002c0003t0008g0045 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2224-731A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 19/19 | chr3 | 160259366 | ||||||
chr3:160259729
|
T | C | 1 | a0002c0002t0002g0055 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2224-1094A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 19/19 | chr3 | 160259729 | ||||||
chr3:160260091
|
A | G | 1 | a0001c0001t0001g0138 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.2224-1456T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 19/19 | chr3 | 160260091 | ||||||
chr3:160260177
|
T | C | 1 | a0002c0006t0002g0014 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2224-1542A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 19/19 | chr3 | 160260177 | ||||||
chr3:160260320
|
A | C | 1 | a0001c0001t0001g0191 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.2224-1685T>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 19/19 | chr3 | 160260320 | ||||||
chr3:160260462
|
C | T | 4 | a0002c0002t0001g0033a0002c0002t0002g0003a0002c0002t0002g0034others(1): Show | 5 | HG01243.hp1 HG02723.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.2224-1827G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 19/19 | chr3 | 160260462 | ||||||
chr3:160260791
|
T | C | 1 | a0001c0001t0001g0153 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2224-2156A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 19/19 | chr3 | 160260791 | ||||||
chr3:160260891
|
T | C | 36 | a0002c0002t0001g0033a0002c0002t0002g0003a0002c0002t0002g0004others(33): Show | 39 | HG01069.hp2 HG01243.hp1 HG01255.hp2 others(36): Show |
intron_variant | MODIFIER | c.2224-2256A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 19/19 | chr3 | 160260891 | ||||||
chr3:160261465
|
T | A | 1 | a0002c0006t0002g0014 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2224-2830A>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 19/19 | chr3 | 160261465 | ||||||
chr3:160261474
|
C | T | 2 | a0001c0001t0005g0093a0001c0001t0005g0126 | 2 | HG02809.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.2224-2839G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 19/19 | chr3 | 160261474 | ||||||
chr3:160261685
|
C | T | 1 | a0002c0002t0002g0083 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2224-3050G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 19/19 | chr3 | 160261685 | ||||||
chr3:160261746
|
A | G | 60 | a0002c0002t0001g0033a0002c0002t0002g0003a0002c0002t0002g0004others(57): Show | 63 | HG00738.hp2 HG01069.hp2 HG01167.hp1 others(60): Show |
intron_variant | MODIFIER | c.2224-3111T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 19/19 | chr3 | 160261746 | ||||||
chr3:160261801
|
C | CA | 31 | a0002c0002t0001g0033a0002c0002t0002g0003a0002c0002t0002g0004others(28): Show | 34 | HG01069.hp2 HG01243.hp1 HG01255.hp2 others(31): Show |
intron_variant | MODIFIER | c.2224-3167dupT | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 19/19 | chr3 | 160261801 | ||||||
chr3:160261801
|
C | CAA | 5 | a0002c0002t0002g0083a0002c0002t0003g0030a0002c0002t0003g0031others(2): Show | 5 | HG02451.hp2 HG02486.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.2224-3168_2224-316 others(6): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 19/19 | chr3 | 160261801 | ||||||
chr3:160262032
|
T | C | 2 | a0002c0002t0002g0015a0002c0002t0007g0088 | 2 | HG02486.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.2224-3397A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 19/19 | chr3 | 160262032 | ||||||
chr3:160262061
|
G | A | 1 | a0002c0002t0001g0086 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.2224-3426C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 19/19 | chr3 | 160262061 | ||||||
chr3:160262169
|
C | G | 1 | a0002c0002t0002g0204 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2224-3534G>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 19/19 | chr3 | 160262169 | ||||||
chr3:160262324
|
G | C | 6 | a0002c0002t0004g0018a0002c0002t0004g0019a0002c0002t0004g0020others(3): Show | 6 | HG02976.hp2 NA18960.hp1 NA18983.hp2 others(3): Show |
intron_variant | MODIFIER | c.2224-3689C>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 19/19 | chr3 | 160262324 | ||||||
chr3:160262482
|
G | A | 2 | a0001c0001t0001g0148a0001c0001t0001g0149 | 2 | HG01106.hp1 HG01168.hp2 |
intron_variant | MODIFIER | c.2224-3847C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 19/19 | chr3 | 160262482 | ||||||
chr3:160262495
|
A | AT | 107 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(104): Show | 111 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(108): Show |
intron_variant | MODIFIER | c.2224-3861dupA | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 19/19 | chr3 | 160262495 | ||||||
chr3:160262596
|
A | C | 5 | a0002c0002t0002g0004a0002c0002t0002g0028a0002c0002t0002g0048others(2): Show | 6 | HG01069.hp2 HG02717.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.2224-3961T>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 19/19 | chr3 | 160262596 | ||||||
chr3:160262617
|
G | A | 1 | a0001c0001t0001g0190 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.2224-3982C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 19/19 | chr3 | 160262617 | ||||||
chr3:160262666
|
T | C | 1 | a0003c0004t0002g0027 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2224-4031A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 19/19 | chr3 | 160262666 | ||||||
chr3:160262778
|
A | G | 7 | a0001c0001t0001g0092a0001c0001t0001g0174a0001c0001t0001g0176others(4): Show | 7 | HG00735.hp2 HG01070.hp2 HG01109.hp1 others(4): Show |
intron_variant | MODIFIER | c.2224-4143T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 19/19 | chr3 | 160262778 | ||||||
chr3:160262822
|
C | T | 1 | a0002c0002t0002g0055 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2224-4187G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 19/19 | chr3 | 160262822 | ||||||
chr3:160262876
|
A | C | 202 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(199): Show | 209 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(206): Show |
intron_variant | MODIFIER | c.2224-4241T>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 19/19 | chr3 | 160262876 | ||||||
chr3:160262964
|
C | T | 1 | a0002c0003t0008g0045 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2224-4329G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 19/19 | chr3 | 160262964 | ||||||
chr3:160263002
|
T | A | 1 | a0001c0001t0001g0141 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.2224-4367A>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 19/19 | chr3 | 160263002 | ||||||
chr3:160263059
|
C | T | 2 | a0001c0001t0001g0174a0001c0001t0001g0183 | 2 | HG03654.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.2224-4424G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 19/19 | chr3 | 160263059 | ||||||
chr3:160263133
|
T | C | 20 | a0002c0002t0002g0004a0002c0002t0002g0021a0002c0002t0002g0022others(17): Show | 21 | HG01069.hp2 HG01255.hp2 HG02055.hp1 others(18): Show |
intron_variant | MODIFIER | c.2224-4498A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 19/19 | chr3 | 160263133 | ||||||
chr3:160263365
|
C | T | 1 | a0002c0006t0002g0014 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2224-4730G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 19/19 | chr3 | 160263365 | ||||||
chr3:160263399
|
T | C | 2 | a0001c0001t0005g0093a0001c0001t0005g0126 | 2 | HG02809.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.2224-4764A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 19/19 | chr3 | 160263399 | ||||||
chr3:160263428
|
C | T | 3 | a0002c0003t0002g0079a0002c0003t0002g0080a0002c0003t0002g0081 | 3 | HG00738.hp2 HG01167.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.2224-4793G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 19/19 | chr3 | 160263428 | ||||||
chr3:160263464
|
C | T | 15 | a0002c0002t0001g0033a0002c0002t0002g0003a0002c0002t0002g0032others(12): Show | 17 | HG01243.hp1 HG02451.hp2 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.2224-4829G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 19/19 | chr3 | 160263464 | ||||||
chr3:160263494
|
C | T | 1 | a0002c0002t0002g0083 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2224-4859G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 19/19 | chr3 | 160263494 | ||||||
chr3:160263892
|
C | T | 2 | a0002c0002t0003g0038a0002c0002t0003g0039 | 2 | HG02486.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.2223+4521G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 19/19 | chr3 | 160263892 | ||||||
chr3:160264086
|
G | A | 1 | a0002c0002t0003g0029 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2223+4327C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 19/19 | chr3 | 160264086 | ||||||
chr3:160264599
|
CT | C | 53 | a0002c0002t0001g0033a0002c0002t0002g0003a0002c0002t0002g0004others(50): Show | 56 | HG01069.hp2 HG01167.hp2 HG01169.hp1 others(53): Show |
intron_variant | MODIFIER | c.2223+3813delA | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 19/19 | chr3 | 160264599 | ||||||
chr3:160264719
|
T | C | 60 | a0002c0002t0001g0033a0002c0002t0002g0003a0002c0002t0002g0004others(57): Show | 63 | HG00738.hp2 HG01069.hp2 HG01167.hp1 others(60): Show |
intron_variant | MODIFIER | c.2223+3694A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 19/19 | chr3 | 160264719 | ||||||
chr3:160265044
|
A | T | 1 | a0002c0002t0003g0029 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2223+3369T>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 19/19 | chr3 | 160265044 | ||||||
chr3:160265627
|
T | C | 3 | a0002c0003t0002g0079a0002c0003t0002g0080a0002c0003t0002g0081 | 3 | HG00738.hp2 HG01167.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.2223+2786A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 19/19 | chr3 | 160265627 | ||||||
chr3:160265703
|
G | A | 2 | a0002c0002t0002g0023a0002c0002t0002g0025 | 2 | HG02280.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.2223+2710C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 19/19 | chr3 | 160265703 | ||||||
chr3:160265941
|
G | A | 16 | a0002c0002t0001g0033a0002c0002t0002g0003a0002c0002t0002g0032others(13): Show | 18 | HG01243.hp1 HG02451.hp2 HG02486.hp2 others(15): Show |
intron_variant | MODIFIER | c.2223+2472C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 19/19 | chr3 | 160265941 | ||||||
chr3:160266082
|
A | T | 5 | a0002c0002t0002g0156a0002c0002t0002g0157a0002c0002t0002g0158others(2): Show | 5 | HG01167.hp2 HG01169.hp1 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.2223+2331T>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 19/19 | chr3 | 160266082 | ||||||
chr3:160266283
|
T | A | 7 | a0002c0002t0002g0172a0002c0002t0002g0173a0002c0002t0002g0201others(4): Show | 7 | HG02258.hp2 HG02630.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.2223+2130A>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 19/19 | chr3 | 160266283 | ||||||
chr3:160266313
|
T | G | 5 | a0002c0002t0002g0156a0002c0002t0002g0157a0002c0002t0002g0158others(2): Show | 5 | HG01167.hp2 HG01169.hp1 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.2223+2100A>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 19/19 | chr3 | 160266313 | ||||||
chr3:160266339
|
TC | T | 74 | a0001c0001t0001g0006a0001c0001t0001g0016a0001c0001t0001g0092others(71): Show | 78 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(75): Show |
intron_variant | MODIFIER | c.2223+2073delG | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 19/19 | chr3 | 160266339 | ||||||
chr3:160266566
|
T | G | 3 | a0002c0002t0001g0076a0002c0002t0001g0077a0002c0002t0001g0078 | 3 | HG02622.hp1 HG02818.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.2223+1847A>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 19/19 | chr3 | 160266566 | ||||||
chr3:160266822
|
T | C | 1 | a0001c0001t0001g0101 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2223+1591A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 19/19 | chr3 | 160266822 | ||||||
chr3:160266971
|
T | G | 8 | a0002c0002t0002g0021a0002c0002t0002g0022a0002c0002t0002g0023others(5): Show | 8 | HG01255.hp2 HG02055.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.2223+1442A>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 19/19 | chr3 | 160266971 | ||||||
chr3:160267208
|
T | C | 8 | a0002c0002t0002g0021a0002c0002t0002g0022a0002c0002t0002g0023others(5): Show | 8 | HG01255.hp2 HG02055.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.2223+1205A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 19/19 | chr3 | 160267208 | ||||||
chr3:160267219
|
C | T | 22 | a0002c0002t0002g0156a0002c0002t0002g0157a0002c0002t0002g0158others(19): Show | 22 | HG00738.hp2 HG01167.hp1 HG01167.hp2 others(19): Show |
intron_variant | MODIFIER | c.2223+1194G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 19/19 | chr3 | 160267219 | ||||||
chr3:160267353
|
A | T | 16 | a0002c0002t0002g0172a0002c0002t0002g0173a0002c0002t0002g0201others(13): Show | 16 | HG00738.hp2 HG01167.hp1 HG01261.hp1 others(13): Show |
intron_variant | MODIFIER | c.2223+1060T>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 19/19 | chr3 | 160267353 | ||||||
chr3:160267387
|
T | A | 1 | a0001c0001t0001g0112 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.2223+1026A>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 19/19 | chr3 | 160267387 | ||||||
chr3:160267387
|
T | C | 1 | a0001c0001t0001g0124 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2223+1026A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 19/19 | chr3 | 160267387 | ||||||
chr3:160267737
|
T | C | 1 | a0002c0002t0002g0055 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2223+676A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 19/19 | chr3 | 160267737 | ||||||
chr3:160267919
|
G | A | 1 | a0001c0001t0001g0132 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.2223+494C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 19/19 | chr3 | 160267919 | ||||||
chr3:160268097
|
G | A | 1 | a0002c0002t0002g0204 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2223+316C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 19/19 | chr3 | 160268097 | ||||||
chr3:160268360
|
G | A | 4 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0001t0001g0123others(1): Show | 4 | HG01243.hp2 HG03041.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.2223+53C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 19/19 | chr3 | 160268360 | ||||||
chr3:160268377
|
C | T | 1 | a0001c0001t0001g0101 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2223+36G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 19/19 | chr3 | 160268377 | ||||||
chr3:160268642
|
T | C | 1 | a0002c0002t0002g0037 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2100-106A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 18/19 | chr3 | 160268642 | ||||||
chr3:160269222
|
CA | C | 60 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(57): Show | 63 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(60): Show |
intron_variant | MODIFIER | c.2100-687delT | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 18/19 | chr3 | 160269222 | ||||||
chr3:160269222
|
CAA | C | 44 | a0002c0002t0002g0004a0002c0002t0002g0015a0002c0002t0002g0021others(41): Show | 45 | HG00738.hp2 HG01069.hp2 HG01167.hp1 others(42): Show |
intron_variant | MODIFIER | c.2100-688_2100-687d others(4): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 18/19 | chr3 | 160269222 | ||||||
chr3:160269600
|
T | C | 1 | a0001c0001t0001g0141 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.2100-1064A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 18/19 | chr3 | 160269600 | ||||||
chr3:160270050
|
G | A | 1 | a0001c0001t0001g0102 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.2100-1514C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 18/19 | chr3 | 160270050 | ||||||
chr3:160270197
|
C | T | 1 | a0002c0002t0002g0015 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2100-1661G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 18/19 | chr3 | 160270197 | ||||||
chr3:160271016
|
TATG | T | 5 | a0002c0002t0002g0156a0002c0002t0002g0157a0002c0002t0002g0158others(2): Show | 5 | HG01167.hp2 HG01169.hp1 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.2100-2483_2100-248 others(7): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 18/19 | chr3 | 160271016 | ||||||
chr3:160271568
|
C | A | 1 | a0001c0001t0001g0141 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.2100-3032G>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 18/19 | chr3 | 160271568 | ||||||
chr3:160271941
|
CA | C | 25 | a0001c0001t0001g0106a0002c0002t0001g0046a0002c0002t0001g0047others(22): Show | 25 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(22): Show |
intron_variant | MODIFIER | c.2100-3406delT | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 18/19 | chr3 | 160271941 | ||||||
chr3:160271960
|
A | G | 2 | a0002c0002t0002g0015a0002c0002t0007g0088 | 2 | HG02486.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.2100-3424T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 18/19 | chr3 | 160271960 | ||||||
chr3:160272043
|
G | T | 3 | a0001c0001t0001g0116a0001c0001t0001g0117a0001c0001t0001g0118 | 3 | HG01981.hp2 HG03490.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.2100-3507C>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 18/19 | chr3 | 160272043 | ||||||
chr3:160272531
|
T | A | 1 | a0002c0002t0002g0201 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2100-3995A>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 18/19 | chr3 | 160272531 | ||||||
chr3:160272560
|
C | T | 36 | a0002c0002t0001g0033a0002c0002t0002g0003a0002c0002t0002g0004others(33): Show | 39 | HG01069.hp2 HG01243.hp1 HG01255.hp2 others(36): Show |
intron_variant | MODIFIER | c.2100-4024G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 18/19 | chr3 | 160272560 | ||||||
chr3:160272688
|
C | T | 1 | a0002c0006t0002g0014 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2100-4152G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 18/19 | chr3 | 160272688 | ||||||
chr3:160272737
|
T | C | 2 | a0002c0002t0002g0048a0002c0002t0002g0082 | 2 | HG01069.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.2100-4201A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 18/19 | chr3 | 160272737 | ||||||
chr3:160272854
|
A | C | 25 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(22): Show | 27 | HG00099.hp2 HG00323.hp1 HG01243.hp1 others(24): Show |
intron_variant | MODIFIER | c.2100-4318T>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 18/19 | chr3 | 160272854 | ||||||
chr3:160273051
|
C | T | 8 | a0002c0002t0002g0021a0002c0002t0002g0022a0002c0002t0002g0023others(5): Show | 8 | HG01255.hp2 HG02055.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.2099+4255G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 18/19 | chr3 | 160273051 | ||||||
chr3:160273087
|
T | C | 1 | a0002c0002t0002g0082 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.2099+4219A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 18/19 | chr3 | 160273087 | ||||||
chr3:160273222
|
A | G | 5 | a0002c0002t0002g0004a0002c0002t0002g0028a0002c0002t0002g0048others(2): Show | 6 | HG01069.hp2 HG02717.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.2099+4084T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 18/19 | chr3 | 160273222 | ||||||
chr3:160273326
|
C | T | 1 | a0001c0001t0001g0199 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.2099+3980G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 18/19 | chr3 | 160273326 | ||||||
chr3:160273394
|
G | GTAGAT | 25 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(22): Show | 27 | HG00099.hp2 HG00323.hp1 HG01243.hp1 others(24): Show |
intron_variant | MODIFIER | c.2099+3907_2099+391 others(9): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 18/19 | chr3 | 160273394 | ||||||
chr3:160273636
|
A | T | 1 | a0002c0002t0002g0204 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2099+3670T>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 18/19 | chr3 | 160273636 | ||||||
chr3:160273682
|
T | C | 198 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(195): Show | 205 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(202): Show |
intron_variant | MODIFIER | c.2099+3624A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 18/19 | chr3 | 160273682 | ||||||
chr3:160273724
|
A | G | 69 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(66): Show | 72 | HG00099.hp2 HG00323.hp1 HG00738.hp2 others(69): Show |
intron_variant | MODIFIER | c.2099+3582T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 18/19 | chr3 | 160273724 | ||||||
chr3:160273832
|
T | G | 2 | a0002c0002t0002g0015a0002c0002t0007g0088 | 2 | HG02486.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.2099+3474A>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 18/19 | chr3 | 160273832 | ||||||
chr3:160273865
|
G | A | 4 | a0002c0002t0001g0033a0002c0002t0002g0003a0002c0002t0002g0034others(1): Show | 5 | HG01243.hp1 HG02723.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.2099+3441C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 18/19 | chr3 | 160273865 | ||||||
chr3:160274022
|
T | C | 2 | a0002c0002t0002g0015a0002c0002t0007g0088 | 2 | HG02486.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.2099+3284A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 18/19 | chr3 | 160274022 | ||||||
chr3:160274256
|
T | C | 1 | a0002c0002t0002g0034 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2099+3050A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 18/19 | chr3 | 160274256 | ||||||
chr3:160274677
|
G | A | 1 | a0001c0001t0001g0111 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.2099+2629C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 18/19 | chr3 | 160274677 | ||||||
chr3:160274768
|
G | A | 25 | a0002c0002t0001g0046a0002c0002t0001g0047a0002c0002t0001g0056others(22): Show | 25 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(22): Show |
intron_variant | MODIFIER | c.2099+2538C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 18/19 | chr3 | 160274768 | ||||||
chr3:160274856
|
G | A | 2 | a0001c0001t0001g0008a0001c0001t0001g0009 | 2 | HG00099.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.2099+2450C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 18/19 | chr3 | 160274856 | ||||||
chr3:160274927
|
C | A | 15 | a0002c0002t0001g0033a0002c0002t0002g0003a0002c0002t0002g0032others(12): Show | 17 | HG01243.hp1 HG02451.hp2 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.2099+2379G>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 18/19 | chr3 | 160274927 | ||||||
chr3:160274961
|
T | A | 4 | a0002c0002t0002g0202a0002c0002t0002g0203a0002c0002t0002g0204others(1): Show | 4 | HG02258.hp2 HG02965.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.2099+2345A>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 18/19 | chr3 | 160274961 | ||||||
chr3:160274961
|
T | C | 2 | a0002c0002t0004g0042a0002c0002t0004g0043 | 2 | NA18960.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.2099+2345A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 18/19 | chr3 | 160274961 | ||||||
chr3:160275119
|
T | C | 8 | a0001c0001t0001g0005a0001c0001t0001g0161a0001c0001t0001g0162others(5): Show | 9 | HG01433.hp1 HG02257.hp2 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.2099+2187A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 18/19 | chr3 | 160275119 | ||||||
chr3:160275223
|
T | C | 1 | a0002c0002t0002g0055 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2099+2083A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 18/19 | chr3 | 160275223 | ||||||
chr3:160275329
|
G | T | 1 | a0001c0001t0001g0016 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.2099+1977C>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 18/19 | chr3 | 160275329 | ||||||
chr3:160275342
|
T | G | 9 | a0002c0003t0002g0050a0002c0003t0002g0051a0002c0003t0002g0052others(6): Show | 9 | HG00738.hp2 HG01167.hp1 HG01261.hp1 others(6): Show |
intron_variant | MODIFIER | c.2099+1964A>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 18/19 | chr3 | 160275342 | ||||||
chr3:160275424
|
T | C | 1 | a0002c0006t0002g0014 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2099+1882A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 18/19 | chr3 | 160275424 | ||||||
chr3:160275647
|
T | A | 88 | a0002c0002t0001g0033a0002c0002t0001g0046a0002c0002t0001g0047others(85): Show | 91 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(88): Show |
intron_variant | MODIFIER | c.2099+1659A>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 18/19 | chr3 | 160275647 | ||||||
chr3:160275702
|
C | T | 88 | a0002c0002t0001g0033a0002c0002t0001g0046a0002c0002t0001g0047others(85): Show | 91 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(88): Show |
intron_variant | MODIFIER | c.2099+1604G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 18/19 | chr3 | 160275702 | ||||||
chr3:160275735
|
A | G | 2 | a0001c0001t0001g0110a0001c0001t0001g0129 | 2 | HG02293.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.2099+1571T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 18/19 | chr3 | 160275735 | ||||||
chr3:160275784
|
A | G | 9 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(6): Show | 9 | HG00099.hp2 HG00323.hp1 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.2099+1522T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 18/19 | chr3 | 160275784 | ||||||
chr3:160275787
|
G | T | 1 | a0001c0001t0001g0189 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.2099+1519C>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 18/19 | chr3 | 160275787 | ||||||
chr3:160275794
|
AT | A | 2 | a0002c0002t0003g0038a0002c0002t0003g0039 | 2 | HG02486.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.2099+1511delA | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 18/19 | chr3 | 160275794 | ||||||
chr3:160275804
|
A | G | 1 | a0002c0002t0007g0088 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2099+1502T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 18/19 | chr3 | 160275804 | ||||||
chr3:160275987
|
C | A | 8 | a0002c0002t0002g0021a0002c0002t0002g0022a0002c0002t0002g0023others(5): Show | 8 | HG01255.hp2 HG02055.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.2099+1319G>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 18/19 | chr3 | 160275987 | ||||||
chr3:160276160
|
G | A | 1 | a0001c0001t0001g0140 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2099+1146C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 18/19 | chr3 | 160276160 | ||||||
chr3:160276228
|
A | G | 1 | a0002c0002t0007g0088 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2099+1078T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 18/19 | chr3 | 160276228 | ||||||
chr3:160276799
|
T | C | 25 | a0002c0002t0001g0046a0002c0002t0001g0047a0002c0002t0001g0056others(22): Show | 25 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(22): Show |
intron_variant | MODIFIER | c.2099+507A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 18/19 | chr3 | 160276799 | ||||||
chr3:160276975
|
T | C | 24 | a0002c0002t0001g0046a0002c0002t0001g0047a0002c0002t0001g0056others(21): Show | 24 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(21): Show |
intron_variant | MODIFIER | c.2099+331A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 18/19 | chr3 | 160276975 | ||||||
chr3:160276984
|
T | C | 1 | a0001c0001t0001g0171 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.2099+322A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 18/19 | chr3 | 160276984 | ||||||
chr3:160277157
|
T | C | 88 | a0002c0002t0001g0033a0002c0002t0001g0046a0002c0002t0001g0047others(85): Show | 91 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(88): Show |
intron_variant | MODIFIER | c.2099+149A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 18/19 | chr3 | 160277157 | ||||||
chr3:160277511
|
A | G | 1 | a0002c0002t0007g0088 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1927-33T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 17/19 | chr3 | 160277511 | ||||||
chr3:160277568
|
A | G | 37 | a0002c0002t0001g0046a0002c0002t0001g0047a0002c0002t0001g0056others(34): Show | 37 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(34): Show |
intron_variant | MODIFIER | c.1926+13T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 17/19 | chr3 | 160277568 | ||||||
chr3:160277744
|
C | T | 1 | a0001c0001t0001g0089 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1837-74G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 16/19 | chr3 | 160277744 | ||||||
chr3:160277996
|
A | G | 1 | a0002c0002t0002g0055 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1837-326T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 16/19 | chr3 | 160277996 | ||||||
chr3:160278027
|
G | A | 1 | a0001c0001t0001g0111 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1837-357C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 16/19 | chr3 | 160278027 | ||||||
chr3:160278204
|
G | A | 1 | a0001c0001t0001g0136 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1837-534C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 16/19 | chr3 | 160278204 | ||||||
chr3:160278334
|
T | C | 1 | a0001c0001t0001g0133 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1837-664A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 16/19 | chr3 | 160278334 | ||||||
chr3:160278441
|
T | C | 1 | a0002c0002t0001g0067 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1836+752A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 16/19 | chr3 | 160278441 | ||||||
chr3:160278531
|
C | G | 1 | a0002c0002t0002g0083 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1836+662G>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 16/19 | chr3 | 160278531 | ||||||
chr3:160279069
|
TA | T | 8 | a0002c0002t0002g0021a0002c0002t0002g0022a0002c0002t0002g0023others(5): Show | 8 | HG01255.hp2 HG02055.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1836+123delT | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 16/19 | chr3 | 160279069 | ||||||
chr3:160279138
|
AAAGGTAA others(3): Show |
A | 15 | a0002c0002t0001g0033a0002c0002t0002g0003a0002c0002t0002g0032others(12): Show | 17 | HG01243.hp1 HG02451.hp2 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.1836+45_1836+54del others(10): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 16/19 | chr3 | 160279138 | ||||||
chr3:160279676
|
C | CCT | 105 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(102): Show | 109 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(106): Show |
intron_variant | MODIFIER | c.1665-313_1665-312i others(4): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 15/19 | chr3 | 160279676 | ||||||
chr3:160279759
|
C | T | 88 | a0002c0002t0001g0033a0002c0002t0001g0046a0002c0002t0001g0047others(85): Show | 91 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(88): Show |
intron_variant | MODIFIER | c.1665-395G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 15/19 | chr3 | 160279759 | ||||||
chr3:160280323
|
C | A | 1 | a0002c0002t0002g0035 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1664+344G>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 15/19 | chr3 | 160280323 | ||||||
chr3:160280390
|
TG | T | 2 | a0002c0002t0002g0015a0002c0002t0007g0088 | 2 | HG02486.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1664+276delC | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 15/19 | chr3 | 160280390 | ||||||
chr3:160280440
|
G | C | 1 | a0001c0001t0001g0110 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1664+227C>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 15/19 | chr3 | 160280440 | ||||||
chr3:160280453
|
A | G | 1 | a0001c0001t0001g0101 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1664+214T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 15/19 | chr3 | 160280453 | ||||||
chr3:160280583
|
A | C | 1 | a0002c0002t0002g0055 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1664+84T>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 15/19 | chr3 | 160280583 | ||||||
chr3:160280594
|
T | C | 1 | a0002c0002t0007g0088 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1664+73A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 15/19 | chr3 | 160280594 | ||||||
chr3:160281030
|
C | T | 2 | a0002c0002t0002g0015a0002c0002t0007g0088 | 2 | HG02486.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1517-216G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 14/19 | chr3 | 160281030 | ||||||
chr3:160281564
|
C | G | 1 | a0001c0001t0001g0197 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1517-750G>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 14/19 | chr3 | 160281564 | ||||||
chr3:160281656
|
T | C | 3 | a0002c0002t0001g0057a0002c0002t0001g0084a0002c0002t0001g0085 | 3 | HG00099.hp1 HG02602.hp1 HG03490.hp2 |
intron_variant | MODIFIER | c.1516+822A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 14/19 | chr3 | 160281656 | ||||||
chr3:160282271
|
C | A | 2 | a0002c0002t0004g0042a0002c0002t0004g0043 | 2 | NA18960.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.1516+207G>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 14/19 | chr3 | 160282271 | ||||||
chr3:160282369
|
A | G | 2 | a0002c0002t0002g0015a0002c0002t0007g0088 | 2 | HG02486.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1516+109T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 14/19 | chr3 | 160282369 | ||||||
chr3:160282376
|
G | A | 1 | a0001c0001t0001g0152 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.1516+102C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 14/19 | chr3 | 160282376 | ||||||
chr3:160282430
|
A | G | 6 | a0002c0002t0001g0058a0002c0002t0001g0059a0002c0002t0001g0062others(3): Show | 6 | HG00423.hp2 HG00558.hp2 NA18942.hp1 others(3): Show |
intron_variant | MODIFIER | c.1516+48T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 14/19 | chr3 | 160282430 | ||||||
chr3:160282441
|
G | A | 5 | a0002c0002t0002g0004a0002c0002t0002g0028a0002c0002t0002g0048others(2): Show | 6 | HG01069.hp2 HG02717.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1516+37C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 14/19 | chr3 | 160282441 | ||||||
chr3:160283081
|
A | G | 5 | a0002c0002t0002g0004a0002c0002t0002g0028a0002c0002t0002g0048others(2): Show | 6 | HG01069.hp2 HG02717.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1381-468T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 13/19 | chr3 | 160283081 | ||||||
chr3:160283111
|
T | C | 1 | a0002c0002t0007g0088 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1381-498A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 13/19 | chr3 | 160283111 | ||||||
chr3:160283206
|
A | C | 1 | a0001c0001t0001g0144 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1381-593T>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 13/19 | chr3 | 160283206 | ||||||
chr3:160283233
|
A | G | 1 | a0002c0006t0002g0014 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1381-620T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 13/19 | chr3 | 160283233 | ||||||
chr3:160283274
|
T | C | 1 | a0001c0001t0001g0101 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1381-661A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 13/19 | chr3 | 160283274 | ||||||
chr3:160283334
|
C | T | 87 | a0002c0002t0001g0033a0002c0002t0001g0046a0002c0002t0001g0047others(84): Show | 90 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(87): Show |
intron_variant | MODIFIER | c.1381-721G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 13/19 | chr3 | 160283334 | ||||||
chr3:160283578
|
A | G | 15 | a0002c0002t0001g0033a0002c0002t0002g0003a0002c0002t0002g0032others(12): Show | 17 | HG01243.hp1 HG02451.hp2 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.1381-965T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 13/19 | chr3 | 160283578 | ||||||
chr3:160283688
|
C | G | 15 | a0002c0002t0001g0033a0002c0002t0002g0003a0002c0002t0002g0032others(12): Show | 17 | HG01243.hp1 HG02451.hp2 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.1381-1075G>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 13/19 | chr3 | 160283688 | ||||||
chr3:160283869
|
T | C | 1 | a0002c0002t0002g0015 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1381-1256A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 13/19 | chr3 | 160283869 | ||||||
chr3:160284072
|
C | G | 8 | a0002c0002t0002g0021a0002c0002t0002g0022a0002c0002t0002g0023others(5): Show | 8 | HG01255.hp2 HG02055.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1381-1459G>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 13/19 | chr3 | 160284072 | ||||||
chr3:160284140
|
T | G | 1 | a0001c0001t0001g0131 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1381-1527A>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 13/19 | chr3 | 160284140 | ||||||
chr3:160284141
|
G | T | 1 | a0001c0001t0001g0131 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1381-1528C>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 13/19 | chr3 | 160284141 | ||||||
chr3:160284446
|
G | A | 4 | a0001c0001t0001g0005a0001c0001t0001g0161a0001c0001t0001g0162others(1): Show | 5 | HG02257.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1380+1358C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 13/19 | chr3 | 160284446 | ||||||
chr3:160284678
|
T | C | 1 | a0002c0006t0002g0014 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1380+1126A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 13/19 | chr3 | 160284678 | ||||||
chr3:160284774
|
C | T | 2 | a0001c0001t0001g0016a0001c0001t0001g0135 | 2 | HG01261.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.1380+1030G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 13/19 | chr3 | 160284774 | ||||||
chr3:160284780
|
C | T | 2 | a0001c0001t0001g0016a0001c0001t0001g0135 | 2 | HG01261.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.1380+1024G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 13/19 | chr3 | 160284780 | ||||||
chr3:160284821
|
T | G | 2 | a0001c0001t0001g0110a0001c0001t0001g0129 | 2 | HG02293.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.1380+983A>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 13/19 | chr3 | 160284821 | ||||||
chr3:160284854
|
A | C | 5 | a0002c0002t0002g0156a0002c0002t0002g0157a0002c0002t0002g0158others(2): Show | 5 | HG01167.hp2 HG01169.hp1 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.1380+950T>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 13/19 | chr3 | 160284854 | ||||||
chr3:160285067
|
G | C | 2 | a0002c0002t0002g0015a0002c0002t0007g0088 | 2 | HG02486.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1380+737C>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 13/19 | chr3 | 160285067 | ||||||
chr3:160285151
|
C | T | 1 | a0002c0002t0002g0201 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1380+653G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 13/19 | chr3 | 160285151 | ||||||
chr3:160285660
|
G | A | 36 | a0002c0002t0001g0033a0002c0002t0002g0003a0002c0002t0002g0004others(33): Show | 39 | HG01069.hp2 HG01243.hp1 HG01255.hp2 others(36): Show |
intron_variant | MODIFIER | c.1380+144C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 13/19 | chr3 | 160285660 | ||||||
chr3:160285889
|
T | C | 34 | a0001c0001t0001g0006a0001c0001t0001g0168a0001c0001t0001g0169others(31): Show | 35 | HG00323.hp2 HG00423.hp1 HG00642.hp2 others(32): Show |
intron_variant | MODIFIER | c.1316-21A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 12/19 | chr3 | 160285889 | ||||||
chr3:160286111
|
C | T | 1 | a0001c0001t0001g0089 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1316-243G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 12/19 | chr3 | 160286111 | ||||||
chr3:160286238
|
A | G | 129 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(126): Show | 133 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(130): Show |
intron_variant | MODIFIER | c.1316-370T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 12/19 | chr3 | 160286238 | ||||||
chr3:160286251
|
T | C | 1 | a0002c0003t0008g0045 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1316-383A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 12/19 | chr3 | 160286251 | ||||||
chr3:160286419
|
C | T | 6 | a0002c0002t0004g0018a0002c0002t0004g0019a0002c0002t0004g0020others(3): Show | 6 | HG02976.hp2 NA18960.hp1 NA18983.hp2 others(3): Show |
intron_variant | MODIFIER | c.1316-551G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 12/19 | chr3 | 160286419 | ||||||
chr3:160286573
|
T | A | 1 | a0002c0006t0002g0014 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1316-705A>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 12/19 | chr3 | 160286573 | ||||||
chr3:160286580
|
A | C | 1 | a0002c0002t0001g0063 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1316-712T>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 12/19 | chr3 | 160286580 | ||||||
chr3:160286831
|
A | C | 1 | a0002c0002t0002g0083 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1316-963T>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 12/19 | chr3 | 160286831 | ||||||
chr3:160287258
|
T | C | 5 | a0002c0002t0002g0004a0002c0002t0002g0028a0002c0002t0002g0048others(2): Show | 6 | HG01069.hp2 HG02717.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1316-1390A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 12/19 | chr3 | 160287258 | ||||||
chr3:160287269
|
C | T | 1 | a0002c0006t0002g0014 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1316-1401G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 12/19 | chr3 | 160287269 | ||||||
chr3:160287486
|
T | C | 3 | a0002c0003t0002g0079a0002c0003t0002g0080a0002c0003t0002g0081 | 3 | HG00738.hp2 HG01167.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.1316-1618A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 12/19 | chr3 | 160287486 | ||||||
chr3:160287545
|
G | A | 1 | a0001c0001t0001g0124 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1316-1677C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 12/19 | chr3 | 160287545 | ||||||
chr3:160287912
|
G | A | 1 | a0002c0002t0003g0041 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1316-2044C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 12/19 | chr3 | 160287912 | ||||||
chr3:160288070
|
C | T | 1 | a0001c0001t0001g0008 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1316-2202G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 12/19 | chr3 | 160288070 | ||||||
chr3:160288111
|
G | A | 9 | a0002c0002t0002g0015a0002c0002t0002g0172a0002c0002t0002g0173others(6): Show | 9 | HG02258.hp2 HG02486.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.1316-2243C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 12/19 | chr3 | 160288111 | ||||||
chr3:160288563
|
T | C | 45 | a0002c0002t0001g0046a0002c0002t0001g0047a0002c0002t0001g0056others(42): Show | 45 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(42): Show |
intron_variant | MODIFIER | c.1316-2695A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 12/19 | chr3 | 160288563 | ||||||
chr3:160288584
|
T | G | 5 | a0002c0002t0002g0156a0002c0002t0002g0157a0002c0002t0002g0158others(2): Show | 5 | HG01167.hp2 HG01169.hp1 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.1316-2716A>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 12/19 | chr3 | 160288584 | ||||||
chr3:160289433
|
C | T | 1 | a0002c0002t0002g0083 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1316-3565G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 12/19 | chr3 | 160289433 | ||||||
chr3:160289437
|
T | G | 1 | a0001c0001t0001g0161 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1316-3569A>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 12/19 | chr3 | 160289437 | ||||||
chr3:160289557
|
C | G | 1 | a0002c0006t0002g0014 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1316-3689G>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 12/19 | chr3 | 160289557 | ||||||
chr3:160289609
|
C | T | 1 | a0002c0006t0002g0014 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1316-3741G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 12/19 | chr3 | 160289609 | ||||||
chr3:160289612
|
C | T | 1 | a0001c0001t0001g0171 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1316-3744G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 12/19 | chr3 | 160289612 | ||||||
chr3:160289746
|
T | C | 39 | a0001c0001t0001g0006a0001c0001t0001g0168a0001c0001t0001g0169others(36): Show | 40 | HG00323.hp2 HG00423.hp1 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.1316-3878A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 12/19 | chr3 | 160289746 | ||||||
chr3:160289853
|
C | G | 204 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(201): Show | 211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.1316-3985G>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 12/19 | chr3 | 160289853 | ||||||
chr3:160290136
|
C | T | 6 | a0002c0003t0002g0050a0002c0003t0002g0051a0002c0003t0002g0052others(3): Show | 6 | HG01891.hp2 HG02630.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.1316-4268G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 12/19 | chr3 | 160290136 | ||||||
chr3:160290332
|
T | C | 6 | a0002c0002t0004g0018a0002c0002t0004g0019a0002c0002t0004g0020others(3): Show | 6 | HG02976.hp2 NA18960.hp1 NA18983.hp2 others(3): Show |
intron_variant | MODIFIER | c.1316-4464A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 12/19 | chr3 | 160290332 | ||||||
chr3:160290352
|
G | T | 16 | a0002c0002t0001g0033a0002c0002t0002g0003a0002c0002t0002g0032others(13): Show | 18 | HG01243.hp1 HG02451.hp2 HG02486.hp2 others(15): Show |
intron_variant | MODIFIER | c.1316-4484C>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 12/19 | chr3 | 160290352 | ||||||
chr3:160290394
|
C | T | 5 | a0002c0002t0002g0201a0002c0002t0002g0202a0002c0002t0002g0203others(2): Show | 5 | HG02258.hp2 HG02965.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.1316-4526G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 12/19 | chr3 | 160290394 | ||||||
chr3:160290411
|
CAGAAAAA others(5): Show |
C | 1 | a0002c0002t0007g0088 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1316-4555_1316-454 others(16): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 12/19 | chr3 | 160290411 | ||||||
chr3:160290535
|
G | A | 2 | a0001c0001t0006g0198a0002c0002t0002g0083 | 2 | HG02615.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.1316-4667C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 12/19 | chr3 | 160290535 | ||||||
chr3:160290761
|
C | T | 1 | a0001c0001t0001g0132 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.1316-4893G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 12/19 | chr3 | 160290761 | ||||||
chr3:160291498
|
A | G | 1 | a0002c0002t0003g0038 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1316-5630T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 12/19 | chr3 | 160291498 | ||||||
chr3:160291632
|
G | A | 1 | a0002c0002t0002g0049 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1316-5764C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 12/19 | chr3 | 160291632 | ||||||
chr3:160291642
|
C | T | 3 | a0002c0003t0002g0079a0002c0003t0002g0080a0002c0003t0002g0081 | 3 | HG00738.hp2 HG01167.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.1316-5774G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 12/19 | chr3 | 160291642 | ||||||
chr3:160291695
|
T | C | 1 | a0002c0002t0002g0083 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1316-5827A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 12/19 | chr3 | 160291695 | ||||||
chr3:160291744
|
T | C | 1 | a0001c0001t0001g0005 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1316-5876A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 12/19 | chr3 | 160291744 | ||||||
chr3:160291848
|
A | G | 5 | a0002c0002t0002g0156a0002c0002t0002g0157a0002c0002t0002g0158others(2): Show | 5 | HG01167.hp2 HG01169.hp1 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.1316-5980T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 12/19 | chr3 | 160291848 | ||||||
chr3:160291953
|
A | G | 1 | a0001c0001t0001g0181 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1316-6085T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 12/19 | chr3 | 160291953 | ||||||
chr3:160292124
|
C | T | 1 | a0001c0001t0001g0181 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1316-6256G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 12/19 | chr3 | 160292124 | ||||||
chr3:160292254
|
C | T | 1 | a0002c0002t0007g0088 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1316-6386G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 12/19 | chr3 | 160292254 | ||||||
chr3:160292260
|
A | G | 1 | a0002c0002t0002g0044 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1316-6392T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 12/19 | chr3 | 160292260 | ||||||
chr3:160292338
|
A | G | 1 | a0002c0002t0004g0019 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1316-6470T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 12/19 | chr3 | 160292338 | ||||||
chr3:160292451
|
T | C | 5 | a0002c0002t0002g0201a0002c0002t0002g0202a0002c0002t0002g0203others(2): Show | 5 | HG02258.hp2 HG02965.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.1316-6583A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 12/19 | chr3 | 160292451 | ||||||
chr3:160292475
|
C | CT | 9 | a0001c0001t0001g0008a0001c0001t0001g0116a0001c0001t0001g0117others(6): Show | 9 | HG00423.hp1 HG00735.hp2 HG01981.hp2 others(6): Show |
intron_variant | MODIFIER | c.1316-6608dupA | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 12/19 | chr3 | 160292475 | ||||||
chr3:160292475
|
CT | C | 74 | a0001c0001t0001g0152a0001c0001t0001g0154a0001c0001t0001g0191others(71): Show | 76 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(73): Show |
intron_variant | MODIFIER | c.1316-6608delA | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 12/19 | chr3 | 160292475 | ||||||
chr3:160292694
|
G | T | 1 | a0003c0004t0002g0026 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1316-6826C>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 12/19 | chr3 | 160292694 | ||||||
chr3:160292728
|
G | A | 6 | a0002c0002t0001g0033a0002c0002t0002g0003a0002c0002t0002g0032others(3): Show | 7 | HG01243.hp1 HG02723.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.1316-6860C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 12/19 | chr3 | 160292728 | ||||||
chr3:160293124
|
A | G | 15 | a0002c0002t0001g0033a0002c0002t0002g0003a0002c0002t0002g0032others(12): Show | 17 | HG01243.hp1 HG02451.hp2 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.1316-7256T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 12/19 | chr3 | 160293124 | ||||||
chr3:160293351
|
T | C | 8 | a0002c0002t0002g0021a0002c0002t0002g0022a0002c0002t0002g0023others(5): Show | 8 | HG01255.hp2 HG02055.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1316-7483A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 12/19 | chr3 | 160293351 | ||||||
chr3:160293516
|
T | C | 4 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0001t0001g0123others(1): Show | 4 | HG01243.hp2 HG03041.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1315+7367A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 12/19 | chr3 | 160293516 | ||||||
chr3:160293614
|
C | G | 1 | a0001c0001t0001g0166 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1315+7269G>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 12/19 | chr3 | 160293614 | ||||||
chr3:160293688
|
T | C | 1 | a0002c0002t0002g0083 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1315+7195A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 12/19 | chr3 | 160293688 | ||||||
chr3:160294210
|
T | C | 1 | a0001c0001t0001g0141 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1315+6673A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 12/19 | chr3 | 160294210 | ||||||
chr3:160294280
|
G | A | 21 | a0002c0002t0002g0004a0002c0002t0002g0021a0002c0002t0002g0022others(18): Show | 22 | HG01069.hp2 HG01255.hp2 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.1315+6603C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 12/19 | chr3 | 160294280 | ||||||
chr3:160294533
|
C | T | 3 | a0001c0001t0001g0161a0001c0001t0001g0162a0001c0001t0001g0163 | 3 | HG02257.hp2 HG03098.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1315+6350G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 12/19 | chr3 | 160294533 | ||||||
chr3:160294551
|
T | C | 1 | a0002c0002t0002g0032 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1315+6332A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 12/19 | chr3 | 160294551 | ||||||
chr3:160294887
|
GTGCAGTC | G | 3 | a0002c0002t0001g0047a0002c0002t0001g0066a0002c0002t0001g0067 | 3 | HG03710.hp1 HG04184.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.1315+5989_1315+599 others(11): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 12/19 | chr3 | 160294887 | ||||||
chr3:160295021
|
G | A | 1 | a0001c0001t0001g0194 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1315+5862C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 12/19 | chr3 | 160295021 | ||||||
chr3:160295099
|
G | C | 1 | a0001c0001t0001g0109 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1315+5784C>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 12/19 | chr3 | 160295099 | ||||||
chr3:160295423
|
A | AGTGAGCC others(3): Show |
2 | a0002c0002t0002g0048a0002c0002t0002g0082 | 2 | HG01069.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1315+5450_1315+545 others(14): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 12/19 | chr3 | 160295423 | ||||||
chr3:160295544
|
C | T | 1 | a0001c0001t0001g0106 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1315+5339G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 12/19 | chr3 | 160295544 | ||||||
chr3:160295569
|
A | G | 1 | a0002c0002t0007g0088 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1315+5314T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 12/19 | chr3 | 160295569 | ||||||
chr3:160295736
|
A | C | 1 | a0002c0002t0003g0002 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1315+5147T>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 12/19 | chr3 | 160295736 | ||||||
chr3:160295742
|
A | T | 1 | a0002c0002t0002g0083 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1315+5141T>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 12/19 | chr3 | 160295742 | ||||||
chr3:160295981
|
C | G | 1 | a0001c0001t0001g0103 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1315+4902G>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 12/19 | chr3 | 160295981 | ||||||
chr3:160296344
|
A | G | 1 | a0002c0002t0001g0066 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1315+4539T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 12/19 | chr3 | 160296344 | ||||||
chr3:160296542
|
T | C | 1 | a0002c0002t0002g0015 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1315+4341A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 12/19 | chr3 | 160296542 | ||||||
chr3:160296611
|
T | G | 5 | a0002c0002t0002g0156a0002c0002t0002g0157a0002c0002t0002g0158others(2): Show | 5 | HG01167.hp2 HG01169.hp1 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.1315+4272A>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 12/19 | chr3 | 160296611 | ||||||
chr3:160296649
|
T | G | 15 | a0002c0002t0001g0033a0002c0002t0002g0003a0002c0002t0002g0032others(12): Show | 17 | HG01243.hp1 HG02451.hp2 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.1315+4234A>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 12/19 | chr3 | 160296649 | ||||||
chr3:160297080
|
T | C | 1 | a0002c0002t0007g0088 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1315+3803A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 12/19 | chr3 | 160297080 | ||||||
chr3:160297115
|
A | C | 1 | a0001c0001t0001g0094 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1315+3768T>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 12/19 | chr3 | 160297115 | ||||||
chr3:160297116
|
T | A | 8 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0119others(5): Show | 8 | HG00323.hp1 HG01358.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.1315+3767A>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 12/19 | chr3 | 160297116 | ||||||
chr3:160297179
|
C | G | 1 | a0002c0002t0002g0055 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1315+3704G>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 12/19 | chr3 | 160297179 | ||||||
chr3:160297575
|
G | A | 1 | a0002c0006t0002g0014 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1315+3308C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 12/19 | chr3 | 160297575 | ||||||
chr3:160297589
|
C | T | 5 | a0002c0002t0002g0156a0002c0002t0002g0157a0002c0002t0002g0158others(2): Show | 5 | HG01167.hp2 HG01169.hp1 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.1315+3294G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 12/19 | chr3 | 160297589 | ||||||
chr3:160297833
|
G | A | 6 | a0002c0002t0004g0018a0002c0002t0004g0019a0002c0002t0004g0020others(3): Show | 6 | HG02976.hp2 NA18960.hp1 NA18983.hp2 others(3): Show |
intron_variant | MODIFIER | c.1315+3050C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 12/19 | chr3 | 160297833 | ||||||
chr3:160297857
|
T | G | 1 | a0001c0001t0001g0154 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1315+3026A>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 12/19 | chr3 | 160297857 | ||||||
chr3:160297969
|
G | A | 2 | a0002c0002t0003g0030a0002c0002t0003g0031 | 2 | HG02451.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1315+2914C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 12/19 | chr3 | 160297969 | ||||||
chr3:160298061
|
C | A | 1 | a0002c0002t0002g0015 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1315+2822G>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 12/19 | chr3 | 160298061 | ||||||
chr3:160298106
|
G | A | 1 | a0002c0003t0002g0079 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1315+2777C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 12/19 | chr3 | 160298106 | ||||||
chr3:160298147
|
A | G | 1 | a0001c0001t0001g0152 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.1315+2736T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 12/19 | chr3 | 160298147 | ||||||
chr3:160298156
|
A | G | 1 | a0005c0007t0001g0137 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1315+2727T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 12/19 | chr3 | 160298156 | ||||||
chr3:160298339
|
A | G | 6 | a0002c0002t0004g0018a0002c0002t0004g0019a0002c0002t0004g0020others(3): Show | 6 | HG02976.hp2 NA18960.hp1 NA18983.hp2 others(3): Show |
intron_variant | MODIFIER | c.1315+2544T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 12/19 | chr3 | 160298339 | ||||||
chr3:160298350
|
C | A | 1 | a0001c0001t0001g0016 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1315+2533G>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 12/19 | chr3 | 160298350 | ||||||
chr3:160298412
|
CAG | C | 5 | a0002c0002t0002g0156a0002c0002t0002g0157a0002c0002t0002g0158others(2): Show | 5 | HG01167.hp2 HG01169.hp1 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.1315+2469_1315+247 others(6): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 12/19 | chr3 | 160298412 | ||||||
chr3:160298578
|
T | C | 1 | a0001c0001t0001g0131 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1315+2305A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 12/19 | chr3 | 160298578 | ||||||
chr3:160298584
|
CCAGAAAA others(3): Show |
C | 15 | a0002c0002t0001g0033a0002c0002t0002g0003a0002c0002t0002g0032others(12): Show | 17 | HG01243.hp1 HG02451.hp2 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.1315+2289_1315+229 others(14): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 12/19 | chr3 | 160298584 | ||||||
chr3:160298658
|
T | C | 126 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(123): Show | 130 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(127): Show |
intron_variant | MODIFIER | c.1315+2225A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 12/19 | chr3 | 160298658 | ||||||
chr3:160299082
|
C | T | 3 | a0002c0003t0002g0079a0002c0003t0002g0080a0002c0003t0002g0081 | 3 | HG00738.hp2 HG01167.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.1315+1801G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 12/19 | chr3 | 160299082 | ||||||
chr3:160299198
|
A | C | 5 | a0002c0002t0002g0156a0002c0002t0002g0157a0002c0002t0002g0158others(2): Show | 5 | HG01167.hp2 HG01169.hp1 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.1315+1685T>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 12/19 | chr3 | 160299198 | ||||||
chr3:160299510
|
T | A | 5 | a0001c0001t0001g0119a0001c0001t0001g0134a0001c0001t0001g0136others(2): Show | 5 | HG00323.hp1 HG01358.hp2 HG04204.hp1 others(2): Show |
intron_variant | MODIFIER | c.1315+1373A>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 12/19 | chr3 | 160299510 | ||||||
chr3:160299681
|
T | C | 1 | a0001c0001t0001g0130 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1315+1202A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 12/19 | chr3 | 160299681 | ||||||
chr3:160299954
|
C | T | 1 | a0002c0002t0002g0015 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1315+929G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 12/19 | chr3 | 160299954 | ||||||
chr3:160300061
|
C | G | 2 | a0002c0002t0002g0004a0002c0002t0002g0028 | 3 | HG02886.hp2 HG03225.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1315+822G>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 12/19 | chr3 | 160300061 | ||||||
chr3:160300146
|
C | T | 1 | a0001c0001t0001g0180 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1315+737G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 12/19 | chr3 | 160300146 | ||||||
chr3:160300166
|
T | C | 1 | a0002c0006t0002g0014 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1315+717A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 12/19 | chr3 | 160300166 | ||||||
chr3:160300335
|
C | T | 8 | a0002c0002t0002g0021a0002c0002t0002g0022a0002c0002t0002g0023others(5): Show | 8 | HG01255.hp2 HG02055.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1315+548G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 12/19 | chr3 | 160300335 | ||||||
chr3:160300486
|
T | C | 5 | a0002c0002t0002g0156a0002c0002t0002g0157a0002c0002t0002g0158others(2): Show | 5 | HG01167.hp2 HG01169.hp1 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.1315+397A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 12/19 | chr3 | 160300486 | ||||||
chr3:160300736
|
T | C | 1 | a0002c0006t0002g0014 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1315+147A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 12/19 | chr3 | 160300736 | ||||||
chr3:160300823
|
A | G | 1 | a0002c0002t0002g0201 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1315+60T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 12/19 | chr3 | 160300823 | ||||||
chr3:160300854
|
G | C | 7 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(4): Show | 7 | HG00099.hp2 HG02976.hp1 HG03834.hp1 others(4): Show |
intron_variant | MODIFIER | c.1315+29C>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 12/19 | chr3 | 160300854 | ||||||
chr3:160301074
|
C | A | 1 | a0001c0001t0001g0128 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1152-28G>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 11/19 | chr3 | 160301074 | ||||||
chr3:160301172
|
T | C | 1 | a0001c0001t0001g0181 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1152-126A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 11/19 | chr3 | 160301172 | ||||||
chr3:160301348
|
C | A | 5 | a0002c0002t0002g0004a0002c0002t0002g0028a0002c0002t0002g0048others(2): Show | 6 | HG01069.hp2 HG02717.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1152-302G>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 11/19 | chr3 | 160301348 | ||||||
chr3:160301511
|
A | G | 5 | a0002c0003t0002g0050a0002c0003t0002g0051a0002c0003t0002g0052others(2): Show | 5 | HG01891.hp2 HG02630.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.1152-465T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 11/19 | chr3 | 160301511 | ||||||
chr3:160301653
|
A | G | 1 | a0002c0002t0002g0055 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1152-607T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 11/19 | chr3 | 160301653 | ||||||
chr3:160301753
|
T | G | 1 | a0002c0002t0002g0083 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1152-707A>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 11/19 | chr3 | 160301753 | ||||||
chr3:160301760
|
T | G | 2 | a0003c0004t0002g0026a0003c0004t0002g0027 | 2 | HG01255.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1152-714A>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 11/19 | chr3 | 160301760 | ||||||
chr3:160301777
|
A | T | 5 | a0002c0002t0002g0156a0002c0002t0002g0157a0002c0002t0002g0158others(2): Show | 5 | HG01167.hp2 HG01169.hp1 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.1152-731T>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 11/19 | chr3 | 160301777 | ||||||
chr3:160302081
|
T | C | 4 | a0001c0001t0001g0005a0001c0001t0001g0161a0001c0001t0001g0162others(1): Show | 5 | HG02257.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1152-1035A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 11/19 | chr3 | 160302081 | ||||||
chr3:160302292
|
C | A | 1 | a0002c0002t0002g0083 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1152-1246G>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 11/19 | chr3 | 160302292 | ||||||
chr3:160302709
|
G | A | 2 | a0002c0002t0001g0068a0002c0002t0001g0069 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1151+1206C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 11/19 | chr3 | 160302709 | ||||||
chr3:160302711
|
T | C | 1 | a0002c0002t0001g0066 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1151+1204A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 11/19 | chr3 | 160302711 | ||||||
chr3:160302720
|
T | A | 5 | a0002c0002t0002g0156a0002c0002t0002g0157a0002c0002t0002g0158others(2): Show | 5 | HG01167.hp2 HG01169.hp1 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.1151+1195A>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 11/19 | chr3 | 160302720 | ||||||
chr3:160302761
|
T | G | 1 | a0001c0001t0001g0129 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1151+1154A>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 11/19 | chr3 | 160302761 | ||||||
chr3:160302925
|
C | T | 1 | a0002c0006t0002g0014 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1151+990G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 11/19 | chr3 | 160302925 | ||||||
chr3:160302991
|
G | A | 8 | a0001c0001t0001g0005a0001c0001t0001g0161a0001c0001t0001g0162others(5): Show | 9 | HG01433.hp1 HG02257.hp2 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.1151+924C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 11/19 | chr3 | 160302991 | ||||||
chr3:160303090
|
C | A | 7 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(4): Show | 7 | HG00099.hp2 HG02976.hp1 HG03834.hp1 others(4): Show |
intron_variant | MODIFIER | c.1151+825G>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 11/19 | chr3 | 160303090 | ||||||
chr3:160303318
|
G | C | 1 | a0002c0002t0002g0204 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1151+597C>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 11/19 | chr3 | 160303318 | ||||||
chr3:160303363
|
G | T | 5 | a0002c0002t0002g0156a0002c0002t0002g0157a0002c0002t0002g0158others(2): Show | 5 | HG01167.hp2 HG01169.hp1 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.1151+552C>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 11/19 | chr3 | 160303363 | ||||||
chr3:160303520
|
G | A | 1 | a0002c0002t0001g0060 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1151+395C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 11/19 | chr3 | 160303520 | ||||||
chr3:160303726
|
T | A | 5 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0001t0001g0123others(2): Show | 5 | HG01243.hp2 HG02109.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1151+189A>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 11/19 | chr3 | 160303726 | ||||||
chr3:160303893
|
G | A | 126 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(123): Show | 130 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(127): Show |
intron_variant | MODIFIER | c.1151+22C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 11/19 | chr3 | 160303893 | ||||||
chr3:160304194
|
C | T | 1 | a0002c0002t0002g0201 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1077-205G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 10/19 | chr3 | 160304194 | ||||||
chr3:160304340
|
G | A | 22 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(19): Show | 24 | HG00099.hp2 HG01243.hp1 HG02451.hp2 others(21): Show |
intron_variant | MODIFIER | c.1077-351C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 10/19 | chr3 | 160304340 | ||||||
chr3:160304435
|
C | CT | 38 | a0001c0001t0001g0115a0001c0001t0001g0117a0001c0001t0001g0146others(35): Show | 38 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(35): Show |
intron_variant | MODIFIER | c.1077-447dupA | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 10/19 | chr3 | 160304435 | ||||||
chr3:160304616
|
T | C | 1 | a0001c0001t0001g0192 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1077-627A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 10/19 | chr3 | 160304616 | ||||||
chr3:160304809
|
T | C | 1 | a0001c0001t0001g0180 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1077-820A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 10/19 | chr3 | 160304809 | ||||||
chr3:160304812
|
T | C | 3 | a0001c0001t0001g0136a0001c0001t0001g0139a0001c0001t0001g0147 | 3 | HG00323.hp1 HG01358.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.1077-823A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 10/19 | chr3 | 160304812 | ||||||
chr3:160304833
|
T | C | 1 | a0001c0001t0001g0100 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1077-844A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 10/19 | chr3 | 160304833 | ||||||
chr3:160305035
|
C | T | 1 | a0002c0002t0002g0173 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1077-1046G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 10/19 | chr3 | 160305035 | ||||||
chr3:160305108
|
C | T | 3 | a0002c0003t0002g0079a0002c0003t0002g0080a0002c0003t0002g0081 | 3 | HG00738.hp2 HG01167.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.1077-1119G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 10/19 | chr3 | 160305108 | ||||||
chr3:160305202
|
C | A | 1 | a0002c0002t0002g0172 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1077-1213G>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 10/19 | chr3 | 160305202 | ||||||
chr3:160305208
|
C | T | 1 | a0002c0002t0002g0055 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1077-1219G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 10/19 | chr3 | 160305208 | ||||||
chr3:160305532
|
G | C | 32 | a0001c0001t0001g0006a0001c0001t0001g0168a0001c0001t0001g0169others(29): Show | 33 | HG00323.hp2 HG00423.hp1 HG00642.hp2 others(30): Show |
intron_variant | MODIFIER | c.1077-1543C>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 10/19 | chr3 | 160305532 | ||||||
chr3:160305695
|
T | C | 1 | a0002c0002t0002g0156 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1077-1706A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 10/19 | chr3 | 160305695 | ||||||
chr3:160305757
|
T | C | 1 | a0002c0002t0002g0015 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1077-1768A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 10/19 | chr3 | 160305757 | ||||||
chr3:160305968
|
T | C | 2 | a0002c0002t0003g0038a0002c0002t0003g0039 | 2 | HG02486.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1076+1695A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 10/19 | chr3 | 160305968 | ||||||
chr3:160306062
|
A | G | 8 | a0002c0002t0003g0002a0002c0002t0003g0029a0002c0002t0003g0030others(5): Show | 9 | HG02451.hp2 HG02486.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.1076+1601T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 10/19 | chr3 | 160306062 | ||||||
chr3:160306393
|
A | G | 1 | a0002c0002t0002g0028 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1076+1270T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 10/19 | chr3 | 160306393 | ||||||
chr3:160306425
|
T | C | 1 | a0002c0002t0002g0201 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1076+1238A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 10/19 | chr3 | 160306425 | ||||||
chr3:160306494
|
A | G | 2 | a0002c0002t0002g0004a0002c0002t0002g0028 | 3 | HG02886.hp2 HG03225.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1076+1169T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 10/19 | chr3 | 160306494 | ||||||
chr3:160306499
|
C | A | 1 | a0002c0002t0002g0173 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1076+1164G>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 10/19 | chr3 | 160306499 | ||||||
chr3:160306586
|
A | G | 202 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(199): Show | 209 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(206): Show |
intron_variant | MODIFIER | c.1076+1077T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 10/19 | chr3 | 160306586 | ||||||
chr3:160306594
|
A | C | 1 | a0002c0002t0002g0055 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1076+1069T>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 10/19 | chr3 | 160306594 | ||||||
chr3:160306726
|
G | A | 5 | a0002c0002t0002g0156a0002c0002t0002g0157a0002c0002t0002g0158others(2): Show | 5 | HG01167.hp2 HG01169.hp1 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.1076+937C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 10/19 | chr3 | 160306726 | ||||||
chr3:160306997
|
T | A | 1 | a0001c0001t0001g0166 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1076+666A>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 10/19 | chr3 | 160306997 | ||||||
chr3:160307263
|
C | A | 15 | a0002c0002t0001g0033a0002c0002t0002g0003a0002c0002t0002g0032others(12): Show | 17 | HG01243.hp1 HG02451.hp2 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.1076+400G>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 10/19 | chr3 | 160307263 | ||||||
chr3:160307359
|
T | C | 1 | a0002c0002t0007g0088 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1076+304A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 10/19 | chr3 | 160307359 | ||||||
chr3:160307445
|
C | T | 1 | a0002c0002t0002g0083 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1076+218G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 10/19 | chr3 | 160307445 | ||||||
chr3:160307450
|
G | A | 82 | a0001c0001t0001g0006a0001c0001t0001g0168a0001c0001t0001g0169others(79): Show | 83 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(80): Show |
intron_variant | MODIFIER | c.1076+213C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 10/19 | chr3 | 160307450 | ||||||
chr3:160307454
|
A | G | 1 | a0002c0006t0002g0014 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1076+209T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 10/19 | chr3 | 160307454 | ||||||
chr3:160307499
|
C | T | 82 | a0001c0001t0001g0006a0001c0001t0001g0168a0001c0001t0001g0169others(79): Show | 83 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(80): Show |
intron_variant | MODIFIER | c.1076+164G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 10/19 | chr3 | 160307499 | ||||||
chr3:160307622
|
C | G | 1 | a0001c0001t0001g0109 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1076+41G>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 10/19 | chr3 | 160307622 | ||||||
chr3:160307654
|
G | C | 1 | a0002c0002t0002g0015 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1076+9C>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 10/19 | chr3 | 160307654 | ||||||
chr3:160307844
|
G | A | 7 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(4): Show | 7 | HG00099.hp2 HG02976.hp1 HG03834.hp1 others(4): Show |
intron_variant | MODIFIER | c.958-63C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160307844 | ||||||
chr3:160307849
|
C | T | 1 | a0001c0001t0001g0096 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.958-68G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160307849 | ||||||
chr3:160308275
|
A | T | 1 | a0001c0001t0001g0195 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.958-494T>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160308275 | ||||||
chr3:160308291
|
G | T | 1 | a0001c0001t0001g0122 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.958-510C>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160308291 | ||||||
chr3:160308366
|
G | C | 1 | a0001c0001t0001g0133 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.958-585C>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160308366 | ||||||
chr3:160308647
|
T | C | 5 | a0002c0002t0002g0004a0002c0002t0002g0028a0002c0002t0002g0048others(2): Show | 6 | HG01069.hp2 HG02717.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.958-866A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160308647 | ||||||
chr3:160308837
|
G | A | 1 | a0002c0002t0002g0055 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.958-1056C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160308837 | ||||||
chr3:160308842
|
T | C | 39 | a0001c0001t0001g0006a0001c0001t0001g0168a0001c0001t0001g0169others(36): Show | 40 | HG00323.hp2 HG00423.hp1 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.958-1061A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160308842 | ||||||
chr3:160309171
|
C | A | 1 | a0001c0001t0001g0115 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.958-1390G>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160309171 | ||||||
chr3:160309232
|
G | A | 1 | a0002c0002t0002g0082 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.958-1451C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160309232 | ||||||
chr3:160309569
|
C | T | 39 | a0001c0001t0001g0006a0001c0001t0001g0168a0001c0001t0001g0169others(36): Show | 40 | HG00323.hp2 HG00423.hp1 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.958-1788G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160309569 | ||||||
chr3:160309637
|
A | T | 1 | a0005c0007t0001g0137 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.958-1856T>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160309637 | ||||||
chr3:160309729
|
T | C | 1 | a0002c0006t0002g0014 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.958-1948A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160309729 | ||||||
chr3:160309995
|
G | A | 8 | a0001c0001t0001g0017a0001c0001t0001g0094a0001c0001t0001g0095others(5): Show | 8 | HG02109.hp2 HG02258.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.958-2214C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160309995 | ||||||
chr3:160310041
|
C | T | 1 | a0002c0002t0002g0055 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.958-2260G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160310041 | ||||||
chr3:160310226
|
T | C | 126 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(123): Show | 130 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(127): Show |
intron_variant | MODIFIER | c.958-2445A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160310226 | ||||||
chr3:160310368
|
A | G | 3 | a0002c0002t0001g0076a0002c0002t0001g0077a0002c0002t0001g0078 | 3 | HG02622.hp1 HG02818.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.958-2587T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160310368 | ||||||
chr3:160310430
|
G | T | 1 | a0001c0001t0001g0140 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.958-2649C>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160310430 | ||||||
chr3:160310460
|
A | T | 1 | a0001c0001t0001g0115 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.958-2679T>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160310460 | ||||||
chr3:160310659
|
CTA | C | 28 | a0002c0002t0001g0046a0002c0002t0001g0047a0002c0002t0001g0056others(25): Show | 28 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(25): Show |
intron_variant | MODIFIER | c.958-2880_958-2879d others(4): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160310659 | ||||||
chr3:160310685
|
A | G | 1 | a0002c0002t0002g0201 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.958-2904T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160310685 | ||||||
chr3:160310773
|
G | A | 5 | a0002c0002t0002g0156a0002c0002t0002g0157a0002c0002t0002g0158others(2): Show | 5 | HG01167.hp2 HG01169.hp1 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.958-2992C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160310773 | ||||||
chr3:160310844
|
T | C | 1 | a0001c0001t0001g0195 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.958-3063A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160310844 | ||||||
chr3:160311017
|
C | G | 8 | a0002c0002t0002g0021a0002c0002t0002g0022a0002c0002t0002g0023others(5): Show | 8 | HG01255.hp2 HG02055.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.958-3236G>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160311017 | ||||||
chr3:160311134
|
A | C | 20 | a0002c0002t0002g0004a0002c0002t0002g0021a0002c0002t0002g0022others(17): Show | 21 | HG01069.hp2 HG01255.hp2 HG02055.hp1 others(18): Show |
intron_variant | MODIFIER | c.958-3353T>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160311134 | ||||||
chr3:160311187
|
G | T | 1 | a0002c0002t0002g0015 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.958-3406C>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160311187 | ||||||
chr3:160311344
|
A | G | 39 | a0001c0001t0001g0006a0001c0001t0001g0168a0001c0001t0001g0169others(36): Show | 40 | HG00323.hp2 HG00423.hp1 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.958-3563T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160311344 | ||||||
chr3:160311376
|
T | C | 1 | a0002c0002t0007g0088 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.958-3595A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160311376 | ||||||
chr3:160311464
|
T | C | 1 | a0004c0005t0009g0087 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.958-3683A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160311464 | ||||||
chr3:160311533
|
G | A | 19 | a0002c0002t0002g0004a0002c0002t0002g0021a0002c0002t0002g0022others(16): Show | 20 | HG01069.hp2 HG01255.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.958-3752C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160311533 | ||||||
chr3:160311662
|
A | T | 1 | a0001c0001t0001g0115 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.958-3881T>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160311662 | ||||||
chr3:160311893
|
G | A | 1 | a0002c0002t0002g0028 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.958-4112C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160311893 | ||||||
chr3:160312169
|
T | C | 1 | a0001c0001t0001g0187 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.958-4388A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160312169 | ||||||
chr3:160312176
|
G | C | 126 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(123): Show | 130 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(127): Show |
intron_variant | MODIFIER | c.958-4395C>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160312176 | ||||||
chr3:160312355
|
C | T | 5 | a0002c0002t0002g0156a0002c0002t0002g0157a0002c0002t0002g0158others(2): Show | 5 | HG01167.hp2 HG01169.hp1 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.958-4574G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160312355 | ||||||
chr3:160312372
|
A | C | 1 | a0001c0001t0001g0167 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.958-4591T>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160312372 | ||||||
chr3:160312542
|
T | C | 28 | a0002c0002t0001g0046a0002c0002t0001g0047a0002c0002t0001g0056others(25): Show | 28 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(25): Show |
intron_variant | MODIFIER | c.958-4761A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160312542 | ||||||
chr3:160312576
|
T | TATATATA others(30): Show |
1 | a0001c0001t0001g0141 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.958-4832_958-4796d others(39): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160312576 | ||||||
chr3:160312583
|
A | AATATATA others(34): Show |
3 | a0001c0001t0001g0136a0001c0001t0001g0139a0001c0001t0001g0147 | 3 | HG00323.hp1 HG01358.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.958-4843_958-4803d others(43): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160312583 | ||||||
chr3:160312596
|
A | T | 3 | a0001c0001t0001g0116a0001c0001t0001g0117a0001c0001t0001g0118 | 3 | HG01981.hp2 HG03490.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.958-4815T>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160312596 | ||||||
chr3:160312610
|
A | T | 1 | a0001c0001t0001g0115 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.958-4829T>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160312610 | ||||||
chr3:160312611
|
T | A | 1 | a0001c0001t0001g0115 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.958-4830A>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160312611 | ||||||
chr3:160312612
|
A | T | 1 | a0001c0001t0001g0115 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.958-4831T>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160312612 | ||||||
chr3:160312620
|
AAT | A | 50 | a0001c0001t0001g0005a0001c0001t0001g0113a0001c0001t0001g0116others(47): Show | 53 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(50): Show |
intron_variant | MODIFIER | c.958-4841_958-4840d others(4): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160312620 | ||||||
chr3:160312622
|
TATATATA others(39): Show |
T | 1 | a0001c0001t0001g0199 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.958-4887_958-4842d others(48): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160312622 | ||||||
chr3:160312624
|
TATATATA others(37): Show |
T | 76 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(73): Show | 78 | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(75): Show |
intron_variant | MODIFIER | c.958-4887_958-4844d others(46): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160312624 | ||||||
chr3:160312663
|
TATATA | T | 4 | a0002c0002t0003g0031a0002c0003t0002g0079a0002c0003t0002g0080others(1): Show | 4 | HG00738.hp2 HG01167.hp1 HG01261.hp1 others(1): Show |
intron_variant | MODIFIER | c.958-4887_958-4883d others(7): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160312663 | ||||||
chr3:160312665
|
TATA | T | 2 | a0001c0001t0001g0153a0002c0002t0002g0201 | 2 | NA19030.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.958-4887_958-4885d others(5): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160312665 | ||||||
chr3:160312674
|
T | G | 17 | a0001c0001t0001g0005a0001c0001t0001g0100a0001c0001t0001g0101others(14): Show | 18 | HG00323.hp1 HG01358.hp2 HG01433.hp1 others(15): Show |
intron_variant | MODIFIER | c.958-4893A>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160312674 | ||||||
chr3:160312705
|
AATATATA others(39): Show |
A | 2 | a0002c0002t0002g0048a0002c0002t0002g0082 | 2 | HG01069.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.958-4970_958-4925d others(48): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160312705 | ||||||
chr3:160312711
|
TAATATAT others(3): Show |
T | 15 | a0002c0002t0001g0033a0002c0002t0002g0003a0002c0002t0002g0032others(12): Show | 17 | HG01243.hp1 HG02451.hp2 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.958-4940_958-4931d others(12): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160312711 | ||||||
chr3:160312712
|
A | ATATAAAT others(24): Show |
1 | a0002c0002t0002g0015 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.958-4932_958-4931i others(33): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160312712 | ||||||
chr3:160312712
|
AATATATA others(1): Show |
A | 6 | a0002c0002t0002g0055a0002c0002t0002g0083a0002c0003t0002g0079others(3): Show | 6 | HG00738.hp2 HG01167.hp1 HG01261.hp1 others(3): Show |
intron_variant | MODIFIER | c.958-4939_958-4932d others(10): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160312712 | ||||||
chr3:160312721
|
A | T | 6 | a0002c0002t0002g0055a0002c0002t0002g0083a0002c0003t0002g0079others(3): Show | 6 | HG00738.hp2 HG01167.hp1 HG01261.hp1 others(3): Show |
intron_variant | MODIFIER | c.958-4940T>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160312721 | ||||||
chr3:160312728
|
A | G | 22 | a0002c0002t0001g0033a0002c0002t0002g0003a0002c0002t0002g0015others(19): Show | 24 | HG00738.hp2 HG01167.hp1 HG01243.hp1 others(21): Show |
intron_variant | MODIFIER | c.958-4947T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160312728 | ||||||
chr3:160312757
|
T | A | 1 | a0002c0002t0001g0063 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.958-4976A>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160312757 | ||||||
chr3:160312757
|
T | TA | 5 | a0002c0002t0002g0015a0002c0003t0002g0079a0002c0003t0002g0080others(2): Show | 5 | HG00738.hp2 HG01167.hp1 HG01261.hp1 others(2): Show |
intron_variant | MODIFIER | c.958-4977dupT | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160312757 | ||||||
chr3:160312757
|
T | TATA | 15 | a0002c0002t0001g0033a0002c0002t0002g0003a0002c0002t0002g0032others(12): Show | 17 | HG01243.hp1 HG02451.hp2 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.958-4979_958-4977d others(5): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160312757 | ||||||
chr3:160312757
|
T | TATAAATG others(32): Show |
11 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0001g0096others(8): Show | 11 | HG01433.hp1 HG02109.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.958-5015_958-4977d others(41): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160312757 | ||||||
chr3:160312757
|
T | TATAATAA others(35): Show |
1 | a0001c0001t0005g0093 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.958-4977_958-4976i others(44): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160312757 | ||||||
chr3:160312759
|
T | A | 27 | a0002c0002t0001g0046a0002c0002t0001g0047a0002c0002t0001g0056others(24): Show | 27 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(24): Show |
intron_variant | MODIFIER | c.958-4978A>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160312759 | ||||||
chr3:160312764
|
G | A | 1 | a0002c0002t0001g0063 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.958-4983C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160312764 | ||||||
chr3:160312769
|
T | C | 5 | a0002c0002t0002g0156a0002c0002t0002g0157a0002c0002t0002g0158others(2): Show | 5 | HG01167.hp2 HG01169.hp1 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.958-4988A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160312769 | ||||||
chr3:160312785
|
AAT | A | 84 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(81): Show | 85 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(82): Show |
intron_variant | MODIFIER | c.958-5006_958-5005d others(4): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160312785 | ||||||
chr3:160312785
|
AATAT | A | 2 | a0001c0001t0001g0143a0002c0002t0002g0015 | 2 | HG02486.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.958-5008_958-5005d others(6): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160312785 | ||||||
chr3:160312786
|
ATATATAT others(15): Show |
A | 1 | a0002c0006t0002g0014 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.958-5027_958-5006d others(24): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160312786 | ||||||
chr3:160312788
|
A | ATATATAA others(10): Show |
1 | a0002c0002t0001g0063 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.958-5008_958-5007i others(19): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160312788 | ||||||
chr3:160312803
|
G | A | 1 | a0002c0002t0002g0015 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.958-5022C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160312803 | ||||||
chr3:160312824
|
AAT | A | 7 | a0002c0002t0002g0015a0002c0003t0002g0050a0002c0003t0002g0051others(4): Show | 7 | HG01891.hp2 HG02486.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.958-5045_958-5044d others(4): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160312824 | ||||||
chr3:160312824
|
AATAT | A | 18 | a0001c0001t0001g0143a0002c0002t0001g0033a0002c0002t0002g0003others(15): Show | 19 | HG00738.hp2 HG01167.hp1 HG01261.hp1 others(16): Show |
intron_variant | MODIFIER | c.958-5047_958-5044d others(6): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160312824 | ||||||
chr3:160312827
|
A | ATATAATA others(59): Show |
2 | a0002c0002t0003g0002a0002c0002t0003g0040 | 3 | HG02895.hp2 HG02897.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.958-5047_958-5046i others(68): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160312827 | ||||||
chr3:160312828
|
T | TATAATAA others(59): Show |
1 | a0002c0002t0002g0035 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.958-5048_958-5047i others(68): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160312828 | ||||||
chr3:160312828
|
T | TATATATA others(106): Show |
1 | a0001c0001t0001g0017 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.958-5048_958-5047i others(115): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160312828 | ||||||
chr3:160312832
|
TATA | T | 38 | a0001c0001t0001g0006a0001c0001t0001g0168a0001c0001t0001g0169others(35): Show | 39 | HG00323.hp2 HG00423.hp1 HG00642.hp2 others(36): Show |
intron_variant | MODIFIER | c.958-5054_958-5052d others(5): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160312832 | ||||||
chr3:160312842
|
G | A | 19 | a0002c0002t0001g0033a0002c0002t0002g0003a0002c0002t0002g0015others(16): Show | 21 | HG00738.hp2 HG01167.hp1 HG01243.hp1 others(18): Show |
intron_variant | MODIFIER | c.958-5061C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160312842 | ||||||
chr3:160312842
|
G | GTATATTA others(28): Show |
2 | a0001c0001t0001g0130a0002c0002t0007g0088 | 2 | HG03041.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.958-5096_958-5062d others(37): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160312842 | ||||||
chr3:160312842
|
GTATATTA others(28): Show |
G | 2 | a0001c0001t0001g0150a0001c0001t0010g0114 | 2 | HG01069.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.958-5096_958-5062d others(37): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160312842 | ||||||
chr3:160312863
|
A | AAT | 6 | a0002c0002t0002g0083a0002c0002t0003g0002a0002c0002t0003g0040others(3): Show | 7 | HG00738.hp2 HG01167.hp1 HG01261.hp1 others(4): Show |
intron_variant | MODIFIER | c.958-5084_958-5083d others(4): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160312863 | ||||||
chr3:160312863
|
A | AATAT | 4 | a0001c0001t0001g0005a0001c0001t0001g0161a0001c0001t0001g0162others(1): Show | 5 | HG02257.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.958-5086_958-5083d others(6): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160312863 | ||||||
chr3:160312863
|
A | T | 1 | a0002c0002t0002g0035 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.958-5082T>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160312863 | ||||||
chr3:160312877
|
A | G | 6 | a0001c0001t0001g0005a0001c0001t0001g0143a0001c0001t0001g0161others(3): Show | 7 | HG02257.hp2 HG02647.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.958-5096T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160312877 | ||||||
chr3:160312890
|
A | AAATATAT others(70): Show |
1 | a0001c0001t0001g0101 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.958-5186_958-5110d others(79): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160312890 | ||||||
chr3:160312898
|
A | AAT | 112 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(109): Show | 115 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(112): Show |
intron_variant | MODIFIER | c.958-5119_958-5118d others(4): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160312898 | ||||||
chr3:160312906
|
A | T | 1 | a0002c0002t0002g0083 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.958-5125T>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160312906 | ||||||
chr3:160312907
|
T | A | 1 | a0002c0002t0002g0083 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.958-5126A>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160312907 | ||||||
chr3:160312909
|
A | T | 1 | a0002c0002t0002g0083 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.958-5128T>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160312909 | ||||||
chr3:160312925
|
A | AAATATAT | 67 | a0001c0001t0001g0006a0001c0001t0001g0168a0001c0001t0001g0169others(64): Show | 68 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(65): Show |
intron_variant | MODIFIER | c.958-5151_958-5145d others(9): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160312925 | ||||||
chr3:160312925
|
A | AAATATAT others(35): Show |
1 | a0001c0001t0001g0103 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.958-5186_958-5145d others(44): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160312925 | ||||||
chr3:160312925
|
A | T | 1 | a0002c0002t0002g0055 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.958-5144T>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160312925 | ||||||
chr3:160312933
|
A | AAT | 15 | a0002c0002t0002g0156a0002c0002t0002g0157a0002c0002t0002g0158others(12): Show | 15 | HG00738.hp2 HG01167.hp1 HG01167.hp2 others(12): Show |
intron_variant | MODIFIER | c.958-5154_958-5153d others(4): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160312933 | ||||||
chr3:160312933
|
A | T | 7 | a0002c0002t0001g0033a0002c0002t0002g0003a0002c0002t0002g0032others(4): Show | 8 | HG02486.hp2 HG02647.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.958-5152T>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160312933 | ||||||
chr3:160312935
|
TATATAAT others(2): Show |
T | 7 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(4): Show | 7 | HG00099.hp2 HG02976.hp1 HG03834.hp1 others(4): Show |
intron_variant | MODIFIER | c.958-5163_958-5155d others(11): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160312935 | ||||||
chr3:160312941
|
A | T | 19 | a0002c0002t0002g0004a0002c0002t0002g0022a0002c0002t0002g0023others(16): Show | 20 | HG01069.hp2 HG01255.hp2 HG02280.hp2 others(17): Show |
intron_variant | MODIFIER | c.958-5160T>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160312941 | ||||||
chr3:160312942
|
T | A | 19 | a0002c0002t0002g0004a0002c0002t0002g0022a0002c0002t0002g0023others(16): Show | 20 | HG01069.hp2 HG01255.hp2 HG02280.hp2 others(17): Show |
intron_variant | MODIFIER | c.958-5161A>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160312942 | ||||||
chr3:160312942
|
TAA | T | 3 | a0002c0002t0002g0035a0002c0002t0003g0002a0002c0002t0003g0040 | 4 | HG01243.hp1 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.958-5163_958-5162d others(4): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160312942 | ||||||
chr3:160312943
|
A | T | 2 | a0002c0002t0002g0021a0002c0002t0002g0044 | 2 | HG02055.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.958-5162T>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160312943 | ||||||
chr3:160312944
|
A | AATATATA others(170): Show |
1 | a0002c0002t0003g0031 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.958-5164_958-5163i others(179): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160312944 | ||||||
chr3:160312944
|
A | AATATATA others(100): Show |
7 | a0002c0002t0001g0033a0002c0002t0002g0003a0002c0002t0002g0032others(4): Show | 8 | HG02486.hp2 HG02647.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.958-5164_958-5163i others(109): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160312944 | ||||||
chr3:160312944
|
A | AATATATA others(135): Show |
4 | a0002c0002t0003g0029a0002c0002t0003g0030a0002c0002t0003g0039others(1): Show | 4 | HG02451.hp2 HG02615.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.958-5164_958-5163i others(144): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160312944 | ||||||
chr3:160312944
|
A | T | 19 | a0002c0002t0002g0004a0002c0002t0002g0022a0002c0002t0002g0023others(16): Show | 20 | HG01069.hp2 HG01255.hp2 HG02280.hp2 others(17): Show |
intron_variant | MODIFIER | c.958-5163T>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160312944 | ||||||
chr3:160312951
|
AT | A | 1 | a0001c0001t0001g0005 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.958-5171delA | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160312951 | ||||||
chr3:160312960
|
AAATATAT | A | 6 | a0002c0003t0002g0050a0002c0003t0002g0051a0002c0003t0002g0052others(3): Show | 6 | HG01891.hp2 HG02630.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.958-5186_958-5180d others(9): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160312960 | ||||||
chr3:160312967
|
T | TAATATAT others(21): Show |
1 | a0002c0002t0002g0015 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.958-5187_958-5186i others(30): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160312967 | ||||||
chr3:160312986
|
A | T | 3 | a0001c0001t0001g0148a0001c0001t0001g0149a0002c0002t0002g0028 | 3 | HG01106.hp1 HG01168.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.958-5205T>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160312986 | ||||||
chr3:160312986
|
AAT | A | 4 | a0002c0002t0002g0202a0002c0002t0002g0203a0002c0002t0002g0204others(1): Show | 4 | HG02258.hp2 HG02965.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.958-5207_958-5206d others(4): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160312986 | ||||||
chr3:160313051
|
TA | T | 7 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(4): Show | 7 | HG00099.hp2 HG02976.hp1 HG03834.hp1 others(4): Show |
intron_variant | MODIFIER | c.958-5271delT | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160313051 | ||||||
chr3:160313148
|
C | T | 1 | a0002c0002t0007g0088 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.958-5367G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160313148 | ||||||
chr3:160313608
|
A | AT | 7 | a0001c0001t0001g0092a0001c0001t0001g0099a0001c0001t0001g0121others(4): Show | 7 | HG01106.hp1 HG01109.hp1 HG01243.hp2 others(4): Show |
intron_variant | MODIFIER | c.958-5828dupA | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160313608 | ||||||
chr3:160313657
|
T | C | 37 | a0002c0002t0001g0046a0002c0002t0001g0047a0002c0002t0001g0056others(34): Show | 37 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(34): Show |
intron_variant | MODIFIER | c.958-5876A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160313657 | ||||||
chr3:160313854
|
C | T | 3 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0145 | 3 | HG02818.hp1 HG03453.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.957+5906G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160313854 | ||||||
chr3:160314035
|
A | G | 6 | a0002c0002t0004g0018a0002c0002t0004g0019a0002c0002t0004g0020others(3): Show | 6 | HG02976.hp2 NA18960.hp1 NA18983.hp2 others(3): Show |
intron_variant | MODIFIER | c.957+5725T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160314035 | ||||||
chr3:160314190
|
C | G | 1 | a0001c0001t0001g0194 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.957+5570G>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160314190 | ||||||
chr3:160314198
|
G | A | 25 | a0002c0002t0001g0046a0002c0002t0001g0047a0002c0002t0001g0056others(22): Show | 25 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(22): Show |
intron_variant | MODIFIER | c.957+5562C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160314198 | ||||||
chr3:160314228
|
T | C | 1 | a0002c0002t0001g0063 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.957+5532A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160314228 | ||||||
chr3:160314453
|
C | G | 5 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(2): Show | 5 | HG00099.hp2 HG03834.hp1 HG04115.hp2 others(2): Show |
intron_variant | MODIFIER | c.957+5307G>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160314453 | ||||||
chr3:160314493
|
G | A | 43 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(40): Show | 46 | HG00099.hp2 HG01069.hp2 HG01243.hp1 others(43): Show |
intron_variant | MODIFIER | c.957+5267C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160314493 | ||||||
chr3:160314566
|
A | G | 1 | a0002c0002t0002g0004 | 2 | HG03225.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.957+5194T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160314566 | ||||||
chr3:160314596
|
C | T | 8 | a0002c0002t0002g0021a0002c0002t0002g0022a0002c0002t0002g0023others(5): Show | 8 | HG01255.hp2 HG02055.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.957+5164G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160314596 | ||||||
chr3:160314599
|
G | A | 1 | a0002c0002t0007g0088 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.957+5161C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160314599 | ||||||
chr3:160314681
|
T | C | 1 | a0001c0001t0001g0105 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.957+5079A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160314681 | ||||||
chr3:160314750
|
C | T | 1 | a0002c0002t0002g0173 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.957+5010G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160314750 | ||||||
chr3:160314755
|
C | T | 1 | a0002c0003t0002g0079 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.957+5005G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160314755 | ||||||
chr3:160315053
|
A | AAGGG | 33 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0091others(30): Show | 35 | HG00140.hp2 HG00642.hp1 HG01069.hp1 others(32): Show |
intron_variant | MODIFIER | c.957+4703_957+4706d others(6): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160315053 | ||||||
chr3:160315053
|
A | AAGGGAGG others(1): Show |
19 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0012others(16): Show | 20 | HG00558.hp1 HG01069.hp2 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.957+4699_957+4706d others(10): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160315053 | ||||||
chr3:160315053
|
A | AAGGGAGG others(5): Show |
57 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0011others(54): Show | 58 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(55): Show |
intron_variant | MODIFIER | c.957+4695_957+4706d others(14): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160315053 | ||||||
chr3:160315053
|
A | AAGGGAGG others(9): Show |
6 | a0001c0001t0001g0103a0001c0001t0001g0116a0001c0001t0001g0185others(3): Show | 6 | HG02055.hp2 HG02922.hp1 HG03490.hp1 others(3): Show |
intron_variant | MODIFIER | c.957+4691_957+4706d others(18): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160315053 | ||||||
chr3:160315053
|
A | AAGGGAGG others(13): Show |
2 | a0001c0001t0006g0198a0002c0002t0002g0049 | 2 | HG02717.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.957+4687_957+4706d others(22): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160315053 | ||||||
chr3:160315053
|
AAGGG | A | 24 | a0001c0001t0001g0094a0001c0001t0001g0119a0001c0001t0001g0161others(21): Show | 26 | HG00423.hp2 HG00558.hp2 HG00738.hp2 others(23): Show |
intron_variant | MODIFIER | c.957+4703_957+4706d others(6): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160315053 | ||||||
chr3:160315053
|
AAGGGAGG others(1): Show |
A | 55 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0134others(52): Show | 56 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(53): Show |
intron_variant | MODIFIER | c.957+4699_957+4706d others(10): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160315053 | ||||||
chr3:160315053
|
AAGGGAGG others(13): Show |
A | 2 | a0002c0002t0002g0037a0002c0002t0002g0055 | 2 | HG02647.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.957+4687_957+4706d others(22): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160315053 | ||||||
chr3:160315059
|
G | GGGAGGGA others(8): Show |
1 | a0001c0001t0001g0115 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.957+4686_957+4700d others(17): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160315059 | ||||||
chr3:160315175
|
T | C | 34 | a0002c0002t0001g0033a0002c0002t0002g0003a0002c0002t0002g0004others(31): Show | 37 | HG01069.hp2 HG01243.hp1 HG01255.hp2 others(34): Show |
intron_variant | MODIFIER | c.957+4585A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160315175 | ||||||
chr3:160315176
|
G | T | 1 | a0002c0002t0002g0015 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.957+4584C>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160315176 | ||||||
chr3:160315177
|
T | A | 1 | a0002c0002t0002g0015 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.957+4583A>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160315177 | ||||||
chr3:160315296
|
G | A | 1 | a0001c0001t0001g0005 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.957+4464C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160315296 | ||||||
chr3:160315809
|
T | A | 1 | a0001c0001t0001g0115 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.957+3951A>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160315809 | ||||||
chr3:160315810
|
A | T | 1 | a0001c0001t0001g0115 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.957+3950T>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160315810 | ||||||
chr3:160315847
|
G | A | 1 | a0002c0002t0002g0083 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.957+3913C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160315847 | ||||||
chr3:160315987
|
G | T | 4 | a0002c0002t0003g0002a0002c0002t0003g0030a0002c0002t0003g0031others(1): Show | 5 | HG02451.hp2 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.957+3773C>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160315987 | ||||||
chr3:160316371
|
G | A | 1 | a0001c0001t0001g0089 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.957+3389C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160316371 | ||||||
chr3:160316767
|
T | A | 2 | a0001c0001t0006g0198a0001c0001t0006g0200 | 2 | NA18747.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.957+2993A>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160316767 | ||||||
chr3:160316786
|
A | G | 81 | a0001c0001t0001g0006a0001c0001t0001g0168a0001c0001t0001g0169others(78): Show | 82 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(79): Show |
intron_variant | MODIFIER | c.957+2974T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160316786 | ||||||
chr3:160316787
|
A | G | 2 | a0001c0001t0006g0198a0001c0001t0006g0200 | 2 | NA18747.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.957+2973T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160316787 | ||||||
chr3:160316925
|
C | T | 1 | a0002c0002t0002g0015 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.957+2835G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160316925 | ||||||
chr3:160317002
|
A | C | 1 | a0002c0002t0007g0088 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.957+2758T>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160317002 | ||||||
chr3:160317152
|
A | G | 1 | a0002c0002t0002g0201 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.957+2608T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160317152 | ||||||
chr3:160317450
|
T | C | 1 | a0001c0001t0001g0102 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.957+2310A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160317450 | ||||||
chr3:160318161
|
T | G | 39 | a0001c0001t0001g0006a0001c0001t0001g0168a0001c0001t0001g0169others(36): Show | 40 | HG00323.hp2 HG00423.hp1 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.957+1599A>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160318161 | ||||||
chr3:160318275
|
G | A | 2 | a0002c0002t0002g0034a0002c0002t0002g0035 | 2 | HG01243.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.957+1485C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160318275 | ||||||
chr3:160318288
|
T | C | 82 | a0001c0001t0001g0006a0001c0001t0001g0168a0001c0001t0001g0169others(79): Show | 83 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(80): Show |
intron_variant | MODIFIER | c.957+1472A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160318288 | ||||||
chr3:160318449
|
G | A | 5 | a0002c0002t0002g0201a0002c0002t0002g0202a0002c0002t0002g0203others(2): Show | 5 | HG02258.hp2 HG02965.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.957+1311C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160318449 | ||||||
chr3:160318612
|
A | G | 126 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(123): Show | 130 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(127): Show |
intron_variant | MODIFIER | c.957+1148T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160318612 | ||||||
chr3:160318660
|
G | C | 126 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(123): Show | 130 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(127): Show |
intron_variant | MODIFIER | c.957+1100C>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160318660 | ||||||
chr3:160318900
|
C | T | 1 | a0002c0002t0002g0015 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.957+860G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160318900 | ||||||
chr3:160319555
|
G | A | 9 | a0002c0002t0002g0037a0002c0002t0003g0002a0002c0002t0003g0029others(6): Show | 10 | HG02451.hp2 HG02486.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.957+205C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160319555 | ||||||
chr3:160319687
|
A | G | 1 | a0002c0002t0002g0172 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.957+73T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160319687 | ||||||
chr3:160320116
|
G | A | 135 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(132): Show | 140 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(137): Show |
intron_variant | MODIFIER | c.778-177C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160320116 | ||||||
chr3:160320184
|
T | A | 44 | a0001c0001t0001g0006a0001c0001t0001g0168a0001c0001t0001g0169others(41): Show | 45 | HG00323.hp2 HG00423.hp1 HG00642.hp2 others(42): Show |
intron_variant | MODIFIER | c.778-245A>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160320184 | ||||||
chr3:160320441
|
T | TA | 5 | a0002c0003t0002g0050a0002c0003t0002g0051a0002c0003t0002g0052others(2): Show | 5 | HG01891.hp2 HG02630.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.778-503dupT | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160320441 | ||||||
chr3:160320525
|
T | C | 1 | a0001c0001t0001g0106 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.778-586A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160320525 | ||||||
chr3:160321340
|
A | G | 1 | a0002c0002t0002g0083 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.778-1401T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160321340 | ||||||
chr3:160321363
|
T | C | 6 | a0002c0002t0004g0018a0002c0002t0004g0019a0002c0002t0004g0020others(3): Show | 6 | HG02976.hp2 NA18960.hp1 NA18983.hp2 others(3): Show |
intron_variant | MODIFIER | c.778-1424A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160321363 | ||||||
chr3:160321388
|
T | G | 5 | a0002c0002t0002g0201a0002c0002t0002g0202a0002c0002t0002g0203others(2): Show | 5 | HG02258.hp2 HG02965.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.778-1449A>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160321388 | ||||||
chr3:160321676
|
C | G | 1 | a0002c0002t0002g0015 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.778-1737G>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160321676 | ||||||
chr3:160321818
|
T | C | 1 | a0001c0001t0001g0182 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.778-1879A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160321818 | ||||||
chr3:160321999
|
G | T | 5 | a0001c0001t0001g0170a0001c0001t0001g0176a0001c0001t0001g0182others(2): Show | 5 | HG00735.hp2 HG01070.hp2 HG01109.hp2 others(2): Show |
intron_variant | MODIFIER | c.778-2060C>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160321999 | ||||||
chr3:160322003
|
G | GTTAT | 14 | a0001c0001t0001g0005a0001c0001t0001g0096a0001c0001t0001g0097others(11): Show | 15 | HG00280.hp2 HG02257.hp2 HG02896.hp2 others(12): Show |
intron_variant | MODIFIER | c.778-2068_778-2065d others(6): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160322003 | ||||||
chr3:160322003
|
GTTAT | G | 44 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(41): Show | 47 | HG00099.hp2 HG01243.hp1 HG01891.hp2 others(44): Show |
intron_variant | MODIFIER | c.778-2068_778-2065d others(6): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160322003 | ||||||
chr3:160322003
|
GTTATTTA others(1): Show |
G | 38 | a0001c0001t0001g0006a0001c0001t0001g0168a0001c0001t0001g0169others(35): Show | 39 | HG00323.hp2 HG00423.hp1 HG00642.hp2 others(36): Show |
intron_variant | MODIFIER | c.778-2072_778-2065d others(10): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160322003 | ||||||
chr3:160322007
|
T | C | 1 | a0002c0002t0001g0033 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.778-2068A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160322007 | ||||||
chr3:160322011
|
T | C | 21 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(18): Show | 23 | HG00099.hp2 HG01243.hp1 HG02451.hp2 others(20): Show |
intron_variant | MODIFIER | c.778-2072A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160322011 | ||||||
chr3:160322079
|
T | C | 1 | a0002c0002t0002g0204 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.778-2140A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160322079 | ||||||
chr3:160322091
|
T | C | 1 | a0001c0001t0010g0114 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.778-2152A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160322091 | ||||||
chr3:160322194
|
C | T | 14 | a0002c0002t0002g0021a0002c0002t0002g0022a0002c0002t0002g0023others(11): Show | 14 | HG01255.hp2 HG02055.hp1 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.778-2255G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160322194 | ||||||
chr3:160322277
|
C | T | 1 | a0001c0001t0001g0165 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.778-2338G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160322277 | ||||||
chr3:160322763
|
GA | G | 3 | a0002c0002t0001g0076a0002c0002t0001g0077a0002c0002t0001g0078 | 3 | HG02622.hp1 HG02818.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.778-2825delT | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160322763 | ||||||
chr3:160322916
|
A | T | 39 | a0001c0001t0001g0006a0001c0001t0001g0168a0001c0001t0001g0169others(36): Show | 40 | HG00323.hp2 HG00423.hp1 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.778-2977T>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160322916 | ||||||
chr3:160323002
|
T | C | 1 | a0001c0001t0001g0136 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.778-3063A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160323002 | ||||||
chr3:160323028
|
C | G | 32 | a0001c0001t0001g0006a0001c0001t0001g0168a0001c0001t0001g0169others(29): Show | 33 | HG00323.hp2 HG00423.hp1 HG00642.hp2 others(30): Show |
intron_variant | MODIFIER | c.778-3089G>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160323028 | ||||||
chr3:160323152
|
G | C | 1 | a0002c0003t0008g0045 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.778-3213C>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160323152 | ||||||
chr3:160323251
|
A | G | 1 | a0002c0002t0004g0043 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.778-3312T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160323251 | ||||||
chr3:160323290
|
G | C | 2 | a0002c0003t0002g0050a0002c0003t0002g0051 | 2 | HG02630.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.778-3351C>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160323290 | ||||||
chr3:160323318
|
C | G | 6 | a0002c0002t0004g0018a0002c0002t0004g0019a0002c0002t0004g0020others(3): Show | 6 | HG02976.hp2 NA18960.hp1 NA18983.hp2 others(3): Show |
intron_variant | MODIFIER | c.778-3379G>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160323318 | ||||||
chr3:160323323
|
G | C | 6 | a0002c0002t0004g0018a0002c0002t0004g0019a0002c0002t0004g0020others(3): Show | 6 | HG02976.hp2 NA18960.hp1 NA18983.hp2 others(3): Show |
intron_variant | MODIFIER | c.778-3384C>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160323323 | ||||||
chr3:160323351
|
A | G | 6 | a0002c0002t0004g0018a0002c0002t0004g0019a0002c0002t0004g0020others(3): Show | 6 | HG02976.hp2 NA18960.hp1 NA18983.hp2 others(3): Show |
intron_variant | MODIFIER | c.778-3412T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160323351 | ||||||
chr3:160323354
|
C | T | 6 | a0002c0002t0004g0018a0002c0002t0004g0019a0002c0002t0004g0020others(3): Show | 6 | HG02976.hp2 NA18960.hp1 NA18983.hp2 others(3): Show |
intron_variant | MODIFIER | c.778-3415G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160323354 | ||||||
chr3:160323355
|
G | C | 6 | a0002c0002t0004g0018a0002c0002t0004g0019a0002c0002t0004g0020others(3): Show | 6 | HG02976.hp2 NA18960.hp1 NA18983.hp2 others(3): Show |
intron_variant | MODIFIER | c.778-3416C>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160323355 | ||||||
chr3:160323356
|
G | A | 6 | a0002c0002t0004g0018a0002c0002t0004g0019a0002c0002t0004g0020others(3): Show | 6 | HG02976.hp2 NA18960.hp1 NA18983.hp2 others(3): Show |
intron_variant | MODIFIER | c.778-3417C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160323356 | ||||||
chr3:160323358
|
A | AT | 6 | a0002c0002t0004g0018a0002c0002t0004g0019a0002c0002t0004g0020others(3): Show | 6 | HG02976.hp2 NA18960.hp1 NA18983.hp2 others(3): Show |
intron_variant | MODIFIER | c.778-3420dupA | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160323358 | ||||||
chr3:160323361
|
A | T | 6 | a0002c0002t0004g0018a0002c0002t0004g0019a0002c0002t0004g0020others(3): Show | 6 | HG02976.hp2 NA18960.hp1 NA18983.hp2 others(3): Show |
intron_variant | MODIFIER | c.778-3422T>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160323361 | ||||||
chr3:160323371
|
G | C | 6 | a0002c0002t0004g0018a0002c0002t0004g0019a0002c0002t0004g0020others(3): Show | 6 | HG02976.hp2 NA18960.hp1 NA18983.hp2 others(3): Show |
intron_variant | MODIFIER | c.778-3432C>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160323371 | ||||||
chr3:160323390
|
A | G | 6 | a0002c0002t0004g0018a0002c0002t0004g0019a0002c0002t0004g0020others(3): Show | 6 | HG02976.hp2 NA18960.hp1 NA18983.hp2 others(3): Show |
intron_variant | MODIFIER | c.778-3451T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160323390 | ||||||
chr3:160323395
|
A | T | 6 | a0002c0002t0004g0018a0002c0002t0004g0019a0002c0002t0004g0020others(3): Show | 6 | HG02976.hp2 NA18960.hp1 NA18983.hp2 others(3): Show |
intron_variant | MODIFIER | c.778-3456T>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160323395 | ||||||
chr3:160323434
|
C | T | 6 | a0002c0002t0004g0018a0002c0002t0004g0019a0002c0002t0004g0020others(3): Show | 6 | HG02976.hp2 NA18960.hp1 NA18983.hp2 others(3): Show |
intron_variant | MODIFIER | c.778-3495G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160323434 | ||||||
chr3:160323435
|
T | C | 6 | a0002c0002t0004g0018a0002c0002t0004g0019a0002c0002t0004g0020others(3): Show | 6 | HG02976.hp2 NA18960.hp1 NA18983.hp2 others(3): Show |
intron_variant | MODIFIER | c.778-3496A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160323435 | ||||||
chr3:160323617
|
A | G | 3 | a0002c0002t0001g0076a0002c0002t0001g0077a0002c0002t0001g0078 | 3 | HG02622.hp1 HG02818.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.778-3678T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160323617 | ||||||
chr3:160323695
|
C | A | 1 | a0001c0001t0001g0154 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.778-3756G>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160323695 | ||||||
chr3:160324307
|
C | A | 1 | a0002c0002t0002g0083 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.778-4368G>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160324307 | ||||||
chr3:160324308
|
C | T | 8 | a0001c0001t0001g0005a0001c0001t0001g0161a0001c0001t0001g0162others(5): Show | 9 | HG01433.hp1 HG02257.hp2 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.778-4369G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160324308 | ||||||
chr3:160324409
|
C | G | 21 | a0002c0002t0002g0004a0002c0002t0002g0021a0002c0002t0002g0022others(18): Show | 22 | HG01069.hp2 HG01255.hp2 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.778-4470G>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160324409 | ||||||
chr3:160324431
|
A | G | 82 | a0001c0001t0001g0006a0001c0001t0001g0168a0001c0001t0001g0169others(79): Show | 83 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(80): Show |
intron_variant | MODIFIER | c.778-4492T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160324431 | ||||||
chr3:160324440
|
T | C | 1 | a0001c0001t0001g0197 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.778-4501A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160324440 | ||||||
chr3:160324525
|
AAAC | A | 7 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(4): Show | 7 | HG00099.hp2 HG02976.hp1 HG03834.hp1 others(4): Show |
intron_variant | MODIFIER | c.778-4589_778-4587d others(5): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160324525 | ||||||
chr3:160324556
|
A | T | 2 | a0002c0002t0003g0030a0002c0002t0003g0031 | 2 | HG02451.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.778-4617T>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160324556 | ||||||
chr3:160324671
|
G | T | 126 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(123): Show | 130 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(127): Show |
intron_variant | MODIFIER | c.778-4732C>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160324671 | ||||||
chr3:160324713
|
C | T | 1 | a0002c0002t0002g0015 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.778-4774G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160324713 | ||||||
chr3:160324822
|
A | T | 5 | a0002c0002t0002g0156a0002c0002t0002g0157a0002c0002t0002g0158others(2): Show | 5 | HG01167.hp2 HG01169.hp1 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.778-4883T>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160324822 | ||||||
chr3:160324837
|
A | T | 5 | a0002c0002t0002g0156a0002c0002t0002g0157a0002c0002t0002g0158others(2): Show | 5 | HG01167.hp2 HG01169.hp1 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.778-4898T>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160324837 | ||||||
chr3:160324863
|
C | T | 1 | a0002c0002t0003g0038 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.778-4924G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160324863 | ||||||
chr3:160324884
|
T | C | 1 | a0002c0002t0002g0015 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.778-4945A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160324884 | ||||||
chr3:160324893
|
C | G | 1 | a0001c0001t0001g0089 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.778-4954G>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160324893 | ||||||
chr3:160324989
|
G | C | 15 | a0002c0002t0001g0033a0002c0002t0002g0003a0002c0002t0002g0032others(12): Show | 17 | HG01243.hp1 HG02451.hp2 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.778-5050C>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160324989 | ||||||
chr3:160324999
|
G | C | 28 | a0002c0002t0001g0046a0002c0002t0001g0047a0002c0002t0001g0056others(25): Show | 28 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(25): Show |
intron_variant | MODIFIER | c.778-5060C>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160324999 | ||||||
chr3:160325003
|
C | G | 1 | a0002c0002t0002g0015 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.778-5064G>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160325003 | ||||||
chr3:160325073
|
G | T | 2 | a0002c0002t0003g0038a0002c0002t0003g0039 | 2 | HG02486.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.778-5134C>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160325073 | ||||||
chr3:160325140
|
G | C | 1 | a0002c0002t0002g0049 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.778-5201C>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160325140 | ||||||
chr3:160325249
|
A | G | 3 | a0002c0003t0002g0079a0002c0003t0002g0080a0002c0003t0002g0081 | 3 | HG00738.hp2 HG01167.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.778-5310T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160325249 | ||||||
chr3:160325668
|
A | G | 126 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(123): Show | 130 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(127): Show |
intron_variant | MODIFIER | c.778-5729T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160325668 | ||||||
chr3:160325751
|
T | C | 15 | a0002c0002t0001g0033a0002c0002t0002g0003a0002c0002t0002g0032others(12): Show | 17 | HG01243.hp1 HG02451.hp2 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.778-5812A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160325751 | ||||||
chr3:160325782
|
T | C | 1 | a0002c0002t0003g0029 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.778-5843A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160325782 | ||||||
chr3:160326044
|
T | C | 5 | a0002c0002t0002g0004a0002c0002t0002g0028a0002c0002t0002g0048others(2): Show | 6 | HG01069.hp2 HG02717.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.778-6105A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160326044 | ||||||
chr3:160326094
|
T | A | 5 | a0002c0002t0002g0156a0002c0002t0002g0157a0002c0002t0002g0158others(2): Show | 5 | HG01167.hp2 HG01169.hp1 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.778-6155A>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160326094 | ||||||
chr3:160326284
|
C | A | 1 | a0001c0001t0001g0101 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.778-6345G>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160326284 | ||||||
chr3:160326432
|
T | C | 8 | a0001c0001t0001g0017a0001c0001t0001g0094a0001c0001t0001g0095others(5): Show | 8 | HG02109.hp2 HG02258.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.778-6493A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160326432 | ||||||
chr3:160326538
|
G | A | 2 | a0002c0003t0002g0080a0002c0003t0002g0081 | 2 | HG00738.hp2 HG01167.hp1 |
intron_variant | MODIFIER | c.778-6599C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160326538 | ||||||
chr3:160326903
|
T | A | 28 | a0002c0002t0001g0046a0002c0002t0001g0047a0002c0002t0001g0056others(25): Show | 28 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(25): Show |
intron_variant | MODIFIER | c.778-6964A>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160326903 | ||||||
chr3:160327279
|
C | T | 22 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(19): Show | 24 | HG00099.hp2 HG01243.hp1 HG02451.hp2 others(21): Show |
intron_variant | MODIFIER | c.778-7340G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160327279 | ||||||
chr3:160327438
|
C | G | 5 | a0001c0001t0001g0119a0001c0001t0001g0134a0001c0001t0001g0136others(2): Show | 5 | HG00323.hp1 HG01358.hp2 HG04204.hp1 others(2): Show |
intron_variant | MODIFIER | c.778-7499G>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160327438 | ||||||
chr3:160327475
|
C | G | 1 | a0002c0002t0002g0204 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.778-7536G>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160327475 | ||||||
chr3:160327628
|
G | C | 3 | a0002c0002t0002g0048a0002c0002t0002g0049a0002c0002t0002g0082 | 3 | HG01069.hp2 HG02717.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.778-7689C>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160327628 | ||||||
chr3:160327695
|
T | C | 1 | a0002c0002t0002g0055 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.778-7756A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160327695 | ||||||
chr3:160327747
|
C | A | 1 | a0001c0001t0001g0016 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.778-7808G>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160327747 | ||||||
chr3:160327785
|
T | C | 22 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(19): Show | 24 | HG00099.hp2 HG01243.hp1 HG02451.hp2 others(21): Show |
intron_variant | MODIFIER | c.778-7846A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160327785 | ||||||
chr3:160327981
|
C | T | 43 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(40): Show | 46 | HG00099.hp2 HG01069.hp2 HG01243.hp1 others(43): Show |
intron_variant | MODIFIER | c.778-8042G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160327981 | ||||||
chr3:160328155
|
C | A | 8 | a0002c0002t0002g0021a0002c0002t0002g0022a0002c0002t0002g0023others(5): Show | 8 | HG01255.hp2 HG02055.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.778-8216G>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160328155 | ||||||
chr3:160328389
|
A | G | 127 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(124): Show | 131 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(128): Show |
intron_variant | MODIFIER | c.778-8450T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160328389 | ||||||
chr3:160328461
|
C | CA | 78 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(75): Show | 81 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(78): Show |
intron_variant | MODIFIER | c.778-8523dupT | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160328461 | ||||||
chr3:160328697
|
G | A | 1 | a0002c0006t0002g0014 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.778-8758C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160328697 | ||||||
chr3:160328774
|
G | C | 1 | a0002c0002t0002g0037 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.778-8835C>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160328774 | ||||||
chr3:160328962
|
A | T | 1 | a0001c0001t0001g0181 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.778-9023T>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160328962 | ||||||
chr3:160328991
|
T | C | 1 | a0002c0002t0002g0083 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.778-9052A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160328991 | ||||||
chr3:160328992
|
G | A | 1 | a0001c0001t0001g0131 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.778-9053C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160328992 | ||||||
chr3:160329211
|
T | C | 1 | a0001c0001t0001g0166 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.778-9272A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160329211 | ||||||
chr3:160329335
|
T | C | 1 | a0002c0002t0001g0063 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.778-9396A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160329335 | ||||||
chr3:160329462
|
C | T | 1 | a0001c0001t0001g0113 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.778-9523G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160329462 | ||||||
chr3:160329518
|
T | C | 81 | a0001c0001t0001g0006a0001c0001t0001g0168a0001c0001t0001g0169others(78): Show | 82 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(79): Show |
intron_variant | MODIFIER | c.778-9579A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160329518 | ||||||
chr3:160329620
|
A | C | 5 | a0002c0002t0002g0004a0002c0002t0002g0028a0002c0002t0002g0048others(2): Show | 6 | HG01069.hp2 HG02717.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.778-9681T>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160329620 | ||||||
chr3:160329652
|
T | C | 126 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(123): Show | 130 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(127): Show |
intron_variant | MODIFIER | c.778-9713A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160329652 | ||||||
chr3:160329671
|
C | T | 2 | a0001c0001t0001g0100a0001c0001t0001g0145 | 2 | HG02818.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.778-9732G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160329671 | ||||||
chr3:160329794
|
T | C | 1 | a0001c0001t0001g0089 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.778-9855A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160329794 | ||||||
chr3:160329824
|
CT | C | 34 | a0001c0001t0001g0006a0001c0001t0001g0168a0001c0001t0001g0169others(31): Show | 35 | HG00323.hp2 HG00423.hp1 HG00642.hp2 others(32): Show |
intron_variant | MODIFIER | c.778-9886delA | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160329824 | ||||||
chr3:160329932
|
T | A | 1 | a0002c0002t0003g0041 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.778-9993A>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160329932 | ||||||
chr3:160330076
|
G | A | 1 | a0002c0002t0003g0039 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.778-10137C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160330076 | ||||||
chr3:160330197
|
C | A | 6 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0175others(3): Show | 6 | HG00323.hp2 HG00642.hp2 HG00738.hp1 others(3): Show |
intron_variant | MODIFIER | c.778-10258G>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160330197 | ||||||
chr3:160330377
|
C | T | 1 | a0002c0002t0001g0084 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.778-10438G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160330377 | ||||||
chr3:160330420
|
A | G | 6 | a0002c0003t0002g0050a0002c0003t0002g0051a0002c0003t0002g0052others(3): Show | 6 | HG01891.hp2 HG02630.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.778-10481T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160330420 | ||||||
chr3:160330530
|
A | G | 1 | a0001c0001t0001g0185 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.778-10591T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160330530 | ||||||
chr3:160330687
|
T | C | 7 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(4): Show | 7 | HG00099.hp2 HG02976.hp1 HG03834.hp1 others(4): Show |
intron_variant | MODIFIER | c.778-10748A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160330687 | ||||||
chr3:160330754
|
C | T | 1 | a0002c0003t0002g0054 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.778-10815G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160330754 | ||||||
chr3:160330886
|
G | A | 1 | a0002c0006t0002g0014 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.778-10947C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160330886 | ||||||
chr3:160330928
|
G | T | 1 | a0002c0002t0002g0055 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.778-10989C>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160330928 | ||||||
chr3:160331111
|
G | A | 2 | a0002c0002t0001g0060a0002c0002t0001g0061 | 2 | HG01361.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.778-11172C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160331111 | ||||||
chr3:160331113
|
C | T | 1 | a0002c0002t0002g0015 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.778-11174G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160331113 | ||||||
chr3:160331228
|
G | A | 1 | a0002c0003t0002g0079 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.778-11289C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160331228 | ||||||
chr3:160331265
|
T | G | 1 | a0001c0001t0001g0101 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.778-11326A>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160331265 | ||||||
chr3:160331379
|
T | C | 1 | a0001c0001t0001g0166 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.778-11440A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160331379 | ||||||
chr3:160331668
|
A | AT | 125 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(122): Show | 129 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(126): Show |
intron_variant | MODIFIER | c.778-11730dupA | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160331668 | ||||||
chr3:160331720
|
A | C | 1 | a0002c0006t0002g0014 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.778-11781T>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160331720 | ||||||
chr3:160332012
|
TC | T | 39 | a0001c0001t0001g0006a0001c0001t0001g0168a0001c0001t0001g0169others(36): Show | 40 | HG00323.hp2 HG00423.hp1 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.778-12074delG | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160332012 | ||||||
chr3:160332039
|
T | A | 1 | a0002c0006t0002g0014 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.778-12100A>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160332039 | ||||||
chr3:160332040
|
C | T | 1 | a0002c0006t0002g0014 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.778-12101G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160332040 | ||||||
chr3:160332045
|
G | A | 1 | a0002c0002t0001g0063 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.778-12106C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160332045 | ||||||
chr3:160332138
|
A | C | 204 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(201): Show | 211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.778-12199T>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160332138 | ||||||
chr3:160332389
|
G | T | 1 | a0002c0002t0002g0083 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.778-12450C>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160332389 | ||||||
chr3:160332878
|
G | A | 19 | a0002c0002t0002g0004a0002c0002t0002g0021a0002c0002t0002g0022others(16): Show | 20 | HG01069.hp2 HG01255.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.778-12939C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160332878 | ||||||
chr3:160332925
|
A | T | 1 | a0002c0002t0007g0088 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.778-12986T>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160332925 | ||||||
chr3:160333036
|
A | G | 39 | a0001c0001t0001g0006a0001c0001t0001g0168a0001c0001t0001g0169others(36): Show | 40 | HG00323.hp2 HG00423.hp1 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.778-13097T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160333036 | ||||||
chr3:160333046
|
T | C | 7 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(4): Show | 7 | HG00099.hp2 HG02976.hp1 HG03834.hp1 others(4): Show |
intron_variant | MODIFIER | c.778-13107A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160333046 | ||||||
chr3:160333076
|
C | T | 1 | a0001c0001t0001g0119 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.778-13137G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160333076 | ||||||
chr3:160333189
|
C | T | 1 | a0002c0002t0002g0037 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.778-13250G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160333189 | ||||||
chr3:160333264
|
T | C | 5 | a0001c0001t0001g0119a0001c0001t0001g0134a0001c0001t0001g0136others(2): Show | 5 | HG00323.hp1 HG01358.hp2 HG04204.hp1 others(2): Show |
intron_variant | MODIFIER | c.778-13325A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160333264 | ||||||
chr3:160333345
|
A | T | 7 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(4): Show | 7 | HG00099.hp2 HG02976.hp1 HG03834.hp1 others(4): Show |
intron_variant | MODIFIER | c.778-13406T>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160333345 | ||||||
chr3:160333434
|
T | C | 1 | a0001c0001t0001g0138 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.778-13495A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160333434 | ||||||
chr3:160333732
|
A | G | 1 | a0002c0006t0002g0014 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.778-13793T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160333732 | ||||||
chr3:160333923
|
C | T | 2 | a0002c0002t0001g0068a0002c0002t0001g0069 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.778-13984G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160333923 | ||||||
chr3:160333988
|
G | A | 2 | a0002c0002t0004g0018a0002c0002t0004g0020 | 2 | NA19084.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.778-14049C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160333988 | ||||||
chr3:160334062
|
G | A | 5 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(2): Show | 5 | HG00099.hp2 HG03834.hp1 HG04115.hp2 others(2): Show |
intron_variant | MODIFIER | c.778-14123C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160334062 | ||||||
chr3:160334428
|
C | CT | 75 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(72): Show | 78 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(75): Show |
intron_variant | MODIFIER | c.778-14490dupA | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160334428 | ||||||
chr3:160334593
|
T | G | 1 | a0001c0001t0001g0184 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.778-14654A>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160334593 | ||||||
chr3:160334606
|
G | A | 3 | a0002c0002t0001g0076a0002c0002t0001g0077a0002c0002t0001g0078 | 3 | HG02622.hp1 HG02818.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.778-14667C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160334606 | ||||||
chr3:160334647
|
C | T | 1 | a0001c0001t0001g0009 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.778-14708G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160334647 | ||||||
chr3:160334690
|
C | G | 1 | a0002c0002t0002g0049 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.778-14751G>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160334690 | ||||||
chr3:160334805
|
CT | C | 118 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(115): Show | 122 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(119): Show |
intron_variant | MODIFIER | c.778-14867delA | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160334805 | ||||||
chr3:160334828
|
T | C | 5 | a0002c0002t0002g0004a0002c0002t0002g0028a0002c0002t0002g0048others(2): Show | 6 | HG01069.hp2 HG02717.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.778-14889A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160334828 | ||||||
chr3:160335021
|
T | C | 1 | a0002c0002t0002g0055 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.778-15082A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160335021 | ||||||
chr3:160335034
|
C | T | 1 | a0001c0001t0001g0141 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.778-15095G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160335034 | ||||||
chr3:160335097
|
C | A | 1 | a0002c0006t0002g0014 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.778-15158G>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160335097 | ||||||
chr3:160335131
|
T | C | 5 | a0002c0003t0002g0050a0002c0003t0002g0051a0002c0003t0002g0052others(2): Show | 5 | HG01891.hp2 HG02630.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.778-15192A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160335131 | ||||||
chr3:160335142
|
A | T | 1 | a0001c0001t0001g0167 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.778-15203T>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160335142 | ||||||
chr3:160335147
|
C | CT | 5 | a0002c0002t0001g0033a0002c0002t0001g0063a0002c0002t0002g0003others(2): Show | 6 | HG01243.hp1 HG02257.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.778-15209dupA | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160335147 | ||||||
chr3:160335449
|
T | C | 5 | a0002c0002t0002g0004a0002c0002t0002g0028a0002c0002t0002g0048others(2): Show | 6 | HG01069.hp2 HG02717.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.778-15510A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160335449 | ||||||
chr3:160335672
|
G | C | 1 | a0002c0002t0002g0015 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.778-15733C>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160335672 | ||||||
chr3:160335744
|
C | T | 37 | a0002c0002t0001g0046a0002c0002t0001g0047a0002c0002t0001g0056others(34): Show | 37 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(34): Show |
intron_variant | MODIFIER | c.778-15805G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160335744 | ||||||
chr3:160335926
|
G | A | 1 | a0002c0002t0001g0046 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.778-15987C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160335926 | ||||||
chr3:160335980
|
A | G | 2 | a0002c0002t0001g0068a0002c0002t0001g0069 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.778-16041T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160335980 | ||||||
chr3:160336156
|
T | C | 1 | a0002c0002t0001g0063 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.778-16217A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160336156 | ||||||
chr3:160336459
|
GAA | G | 5 | a0002c0002t0002g0156a0002c0002t0002g0157a0002c0002t0002g0158others(2): Show | 5 | HG01167.hp2 HG01169.hp1 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.778-16522_778-1652 others(6): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160336459 | ||||||
chr3:160336501
|
T | A | 1 | a0002c0003t0008g0045 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.778-16562A>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160336501 | ||||||
chr3:160336591
|
A | ATGTG | 9 | a0001c0001t0001g0199a0002c0002t0002g0021a0002c0002t0002g0022others(6): Show | 9 | HG01070.hp2 HG01255.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.778-16656_778-1665 others(8): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160336591 | ||||||
chr3:160336764
|
T | C | 5 | a0002c0002t0002g0156a0002c0002t0002g0157a0002c0002t0002g0158others(2): Show | 5 | HG01167.hp2 HG01169.hp1 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.778-16825A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160336764 | ||||||
chr3:160337061
|
T | C | 1 | a0002c0002t0007g0088 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.778-17122A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160337061 | ||||||
chr3:160337156
|
TTA | T | 3 | a0002c0003t0002g0079a0002c0003t0002g0080a0002c0003t0002g0081 | 3 | HG00738.hp2 HG01167.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.778-17219_778-1721 others(6): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160337156 | ||||||
chr3:160337176
|
A | C | 1 | a0001c0001t0001g0007 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.778-17237T>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160337176 | ||||||
chr3:160337363
|
C | T | 6 | a0002c0002t0002g0021a0002c0002t0002g0022a0002c0002t0002g0023others(3): Show | 6 | HG02055.hp1 HG02280.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.778-17424G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160337363 | ||||||
chr3:160337759
|
T | A | 1 | a0002c0006t0002g0014 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.778-17820A>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160337759 | ||||||
chr3:160337770
|
C | T | 4 | a0002c0002t0002g0202a0002c0002t0002g0203a0002c0002t0002g0204others(1): Show | 4 | HG02258.hp2 HG02965.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.778-17831G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160337770 | ||||||
chr3:160338091
|
A | G | 1 | a0002c0002t0002g0083 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.777+17922T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160338091 | ||||||
chr3:160338631
|
C | CA | 9 | a0002c0002t0001g0076a0002c0002t0001g0077a0002c0002t0001g0078others(6): Show | 9 | HG01069.hp2 HG01891.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.777+17381dupT | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160338631 | ||||||
chr3:160338645
|
A | G | 2 | a0002c0002t0003g0030a0002c0002t0003g0031 | 2 | HG02451.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.777+17368T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160338645 | ||||||
chr3:160338743
|
C | A | 1 | a0002c0002t0002g0204 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.777+17270G>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160338743 | ||||||
chr3:160338855
|
G | T | 1 | a0002c0002t0002g0037 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.777+17158C>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160338855 | ||||||
chr3:160338935
|
A | G | 2 | a0002c0002t0004g0018a0002c0002t0004g0020 | 2 | NA19084.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.777+17078T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160338935 | ||||||
chr3:160339325
|
T | A | 1 | a0002c0002t0007g0088 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.777+16688A>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160339325 | ||||||
chr3:160339427
|
T | A | 1 | a0002c0002t0001g0067 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.777+16586A>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160339427 | ||||||
chr3:160339531
|
C | T | 19 | a0002c0002t0002g0004a0002c0002t0002g0021a0002c0002t0002g0022others(16): Show | 20 | HG01069.hp2 HG01255.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.777+16482G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160339531 | ||||||
chr3:160339931
|
G | A | 3 | a0002c0002t0001g0056a0002c0002t0001g0070a0002c0002t0001g0071 | 3 | HG00735.hp1 HG00741.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.777+16082C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160339931 | ||||||
chr3:160340181
|
G | C | 15 | a0002c0002t0001g0033a0002c0002t0002g0003a0002c0002t0002g0032others(12): Show | 17 | HG01243.hp1 HG02451.hp2 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.777+15832C>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160340181 | ||||||
chr3:160340272
|
T | C | 39 | a0001c0001t0001g0006a0001c0001t0001g0168a0001c0001t0001g0169others(36): Show | 40 | HG00323.hp2 HG00423.hp1 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.777+15741A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160340272 | ||||||
chr3:160340338
|
A | G | 1 | a0001c0001t0001g0154 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.777+15675T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160340338 | ||||||
chr3:160340394
|
C | G | 1 | a0002c0002t0002g0015 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.777+15619G>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160340394 | ||||||
chr3:160340484
|
G | A | 1 | a0002c0002t0002g0083 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.777+15529C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160340484 | ||||||
chr3:160340774
|
G | C | 126 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(123): Show | 130 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(127): Show |
intron_variant | MODIFIER | c.777+15239C>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160340774 | ||||||
chr3:160340815
|
C | A | 1 | a0001c0008t0001g0164 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.777+15198G>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160340815 | ||||||
chr3:160341016
|
C | CT | 127 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(124): Show | 131 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(128): Show |
intron_variant | MODIFIER | c.777+14996dupA | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160341016 | ||||||
chr3:160341342
|
TTA | T | 15 | a0002c0002t0001g0033a0002c0002t0002g0003a0002c0002t0002g0032others(12): Show | 17 | HG01243.hp1 HG02451.hp2 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.777+14669_777+1467 others(6): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160341342 | ||||||
chr3:160341343
|
TA | T | 34 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(31): Show | 35 | HG00099.hp2 HG01255.hp2 HG01433.hp1 others(32): Show |
intron_variant | MODIFIER | c.777+14669delT | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160341343 | ||||||
chr3:160341343
|
TAA | T | 81 | a0001c0001t0001g0006a0001c0001t0001g0168a0001c0001t0001g0169others(78): Show | 82 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(79): Show |
intron_variant | MODIFIER | c.777+14668_777+1466 others(6): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160341343 | ||||||
chr3:160341600
|
C | T | 1 | a0002c0002t0003g0040 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.777+14413G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160341600 | ||||||
chr3:160341660
|
A | G | 1 | a0004c0005t0009g0087 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.777+14353T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160341660 | ||||||
chr3:160341849
|
G | A | 1 | a0002c0002t0002g0015 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.777+14164C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160341849 | ||||||
chr3:160341979
|
A | T | 7 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(4): Show | 7 | HG00099.hp2 HG02976.hp1 HG03834.hp1 others(4): Show |
intron_variant | MODIFIER | c.777+14034T>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160341979 | ||||||
chr3:160342003
|
G | A | 8 | a0002c0002t0002g0021a0002c0002t0002g0022a0002c0002t0002g0023others(5): Show | 8 | HG01255.hp2 HG02055.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.777+14010C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160342003 | ||||||
chr3:160342102
|
T | C | 1 | a0002c0002t0002g0015 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.777+13911A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160342102 | ||||||
chr3:160342785
|
T | G | 28 | a0002c0002t0001g0046a0002c0002t0001g0047a0002c0002t0001g0056others(25): Show | 28 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(25): Show |
intron_variant | MODIFIER | c.777+13228A>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160342785 | ||||||
chr3:160342810
|
T | C | 1 | a0002c0002t0002g0055 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.777+13203A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160342810 | ||||||
chr3:160342960
|
C | T | 125 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(122): Show | 129 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(126): Show |
intron_variant | MODIFIER | c.777+13053G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160342960 | ||||||
chr3:160342986
|
T | C | 1 | a0002c0002t0002g0083 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.777+13027A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160342986 | ||||||
chr3:160343150
|
C | T | 6 | a0002c0003t0002g0050a0002c0003t0002g0051a0002c0003t0002g0052others(3): Show | 6 | HG01891.hp2 HG02630.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.777+12863G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160343150 | ||||||
chr3:160343357
|
G | A | 127 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(124): Show | 131 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(128): Show |
intron_variant | MODIFIER | c.777+12656C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160343357 | ||||||
chr3:160343730
|
G | A | 5 | a0002c0002t0002g0156a0002c0002t0002g0157a0002c0002t0002g0158others(2): Show | 5 | HG01167.hp2 HG01169.hp1 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.777+12283C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160343730 | ||||||
chr3:160343754
|
C | T | 1 | a0002c0002t0002g0160 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.777+12259G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160343754 | ||||||
chr3:160343768
|
A | C | 4 | a0002c0002t0002g0157a0002c0002t0002g0158a0002c0002t0002g0159others(1): Show | 4 | HG01167.hp2 HG01169.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.777+12245T>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160343768 | ||||||
chr3:160344039
|
G | A | 3 | a0002c0002t0001g0076a0002c0002t0001g0077a0002c0002t0001g0078 | 3 | HG02622.hp1 HG02818.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.777+11974C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160344039 | ||||||
chr3:160344075
|
A | G | 1 | a0001c0001t0001g0182 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.777+11938T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160344075 | ||||||
chr3:160344106
|
G | C | 1 | a0002c0002t0002g0083 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.777+11907C>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160344106 | ||||||
chr3:160344162
|
C | T | 1 | a0002c0002t0002g0015 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.777+11851G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160344162 | ||||||
chr3:160344245
|
G | A | 1 | a0002c0006t0002g0014 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.777+11768C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160344245 | ||||||
chr3:160344527
|
C | A | 1 | a0002c0002t0002g0083 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.777+11486G>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160344527 | ||||||
chr3:160344618
|
G | A | 1 | a0002c0002t0002g0083 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.777+11395C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160344618 | ||||||
chr3:160344874
|
A | G | 1 | a0001c0008t0001g0164 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.777+11139T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160344874 | ||||||
chr3:160345193
|
T | C | 7 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(4): Show | 7 | HG00099.hp2 HG02976.hp1 HG03834.hp1 others(4): Show |
intron_variant | MODIFIER | c.777+10820A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160345193 | ||||||
chr3:160345277
|
T | C | 1 | a0002c0002t0001g0063 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.777+10736A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160345277 | ||||||
chr3:160345400
|
T | C | 1 | a0002c0002t0002g0055 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.777+10613A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160345400 | ||||||
chr3:160345450
|
G | A | 3 | a0001c0001t0001g0168a0001c0001t0001g0175a0001c0001t0001g0178 | 3 | HG00642.hp2 HG01891.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.777+10563C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160345450 | ||||||
chr3:160345525
|
T | C | 1 | a0001c0001t0001g0109 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.777+10488A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160345525 | ||||||
chr3:160345526
|
A | T | 1 | a0001c0001t0001g0109 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.777+10487T>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160345526 | ||||||
chr3:160345568
|
A | C | 126 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(123): Show | 130 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(127): Show |
intron_variant | MODIFIER | c.777+10445T>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160345568 | ||||||
chr3:160345587
|
G | A | 3 | a0002c0002t0002g0202a0002c0002t0002g0203a0002c0002t0002g0205 | 3 | HG02965.hp2 HG03130.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.777+10426C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160345587 | ||||||
chr3:160345693
|
C | CA | 75 | a0001c0001t0001g0006a0001c0001t0001g0089a0001c0001t0001g0101others(72): Show | 76 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(73): Show |
intron_variant | MODIFIER | c.777+10319dupT | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160345693 | ||||||
chr3:160345693
|
C | CAA | 8 | a0001c0001t0001g0176a0001c0001t0001g0196a0001c0001t0001g0199others(5): Show | 8 | HG01070.hp2 HG01167.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.777+10318_777+1031 others(6): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160345693 | ||||||
chr3:160345693
|
CA | C | 13 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(10): Show | 13 | HG00099.hp2 HG01255.hp2 HG02896.hp1 others(10): Show |
intron_variant | MODIFIER | c.777+10319delT | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160345693 | ||||||
chr3:160345822
|
T | A | 6 | a0002c0003t0002g0050a0002c0003t0002g0051a0002c0003t0002g0052others(3): Show | 6 | HG01891.hp2 HG02630.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.777+10191A>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160345822 | ||||||
chr3:160345961
|
T | C | 5 | a0002c0002t0002g0004a0002c0002t0002g0028a0002c0002t0002g0048others(2): Show | 6 | HG01069.hp2 HG02717.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.777+10052A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160345961 | ||||||
chr3:160346705
|
G | T | 10 | a0001c0001t0001g0089a0001c0001t0001g0115a0001c0001t0001g0116others(7): Show | 10 | HG00280.hp2 HG00741.hp1 HG01106.hp1 others(7): Show |
intron_variant | MODIFIER | c.777+9308C>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160346705 | ||||||
chr3:160346731
|
G | A | 1 | a0002c0006t0002g0014 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.777+9282C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160346731 | ||||||
chr3:160346999
|
G | A | 3 | a0002c0002t0002g0202a0002c0002t0002g0203a0002c0002t0002g0205 | 3 | HG02965.hp2 HG03130.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.777+9014C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160346999 | ||||||
chr3:160347111
|
C | T | 1 | a0001c0001t0001g0135 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.777+8902G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160347111 | ||||||
chr3:160347122
|
C | T | 1 | a0002c0006t0002g0014 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.777+8891G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160347122 | ||||||
chr3:160347334
|
T | C | 1 | a0001c0001t0001g0007 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.777+8679A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160347334 | ||||||
chr3:160347429
|
T | G | 7 | a0001c0001t0001g0017a0001c0001t0001g0095a0001c0001t0001g0096others(4): Show | 7 | HG02258.hp1 HG02622.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.777+8584A>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160347429 | ||||||
chr3:160347629
|
C | G | 1 | a0002c0002t0002g0083 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.777+8384G>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160347629 | ||||||
chr3:160347698
|
A | G | 2 | a0001c0001t0001g0139a0001c0001t0001g0147 | 2 | HG00323.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.777+8315T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160347698 | ||||||
chr3:160347780
|
C | T | 151 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(148): Show | 156 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(153): Show |
intron_variant | MODIFIER | c.777+8233G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160347780 | ||||||
chr3:160347968
|
A | T | 1 | a0002c0002t0002g0055 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.777+8045T>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160347968 | ||||||
chr3:160347975
|
C | T | 1 | a0002c0006t0002g0014 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.777+8038G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160347975 | ||||||
chr3:160347978
|
T | G | 1 | a0002c0002t0002g0055 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.777+8035A>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160347978 | ||||||
chr3:160348074
|
A | G | 8 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0119others(5): Show | 8 | HG00323.hp1 HG01358.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.777+7939T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160348074 | ||||||
chr3:160348198
|
T | C | 1 | a0002c0002t0007g0088 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.777+7815A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160348198 | ||||||
chr3:160348234
|
A | C | 1 | a0002c0002t0002g0083 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.777+7779T>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160348234 | ||||||
chr3:160348240
|
T | C | 1 | a0002c0002t0002g0055 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.777+7773A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160348240 | ||||||
chr3:160349010
|
C | T | 5 | a0002c0002t0002g0004a0002c0002t0002g0028a0002c0002t0002g0048others(2): Show | 6 | HG01069.hp2 HG02717.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.777+7003G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160349010 | ||||||
chr3:160349070
|
T | C | 4 | a0002c0002t0002g0202a0002c0002t0002g0203a0002c0002t0002g0204others(1): Show | 4 | HG02258.hp2 HG02965.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.777+6943A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160349070 | ||||||
chr3:160349108
|
A | AT | 44 | a0001c0001t0001g0006a0001c0001t0001g0168a0001c0001t0001g0169others(41): Show | 45 | HG00323.hp2 HG00423.hp1 HG00642.hp2 others(42): Show |
intron_variant | MODIFIER | c.777+6904dupA | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160349108 | ||||||
chr3:160349586
|
T | A | 8 | a0002c0002t0002g0021a0002c0002t0002g0022a0002c0002t0002g0023others(5): Show | 8 | HG01255.hp2 HG02055.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.777+6427A>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160349586 | ||||||
chr3:160349931
|
T | C | 1 | a0002c0002t0002g0083 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.777+6082A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160349931 | ||||||
chr3:160350142
|
T | C | 127 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(124): Show | 131 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(128): Show |
intron_variant | MODIFIER | c.777+5871A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160350142 | ||||||
chr3:160350243
|
C | T | 3 | a0001c0001t0001g0136a0001c0001t0001g0139a0001c0001t0001g0147 | 3 | HG00323.hp1 HG01358.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.777+5770G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160350243 | ||||||
chr3:160350304
|
T | C | 1 | a0002c0002t0002g0160 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.777+5709A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160350304 | ||||||
chr3:160350340
|
C | T | 5 | a0001c0001t0001g0096a0001c0001t0001g0097a0001c0001t0001g0098others(2): Show | 5 | HG02258.hp1 HG02809.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.777+5673G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160350340 | ||||||
chr3:160350371
|
T | C | 5 | a0002c0002t0002g0156a0002c0002t0002g0157a0002c0002t0002g0158others(2): Show | 5 | HG01167.hp2 HG01169.hp1 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.777+5642A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160350371 | ||||||
chr3:160350415
|
CA | C | 79 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(76): Show | 81 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(78): Show |
intron_variant | MODIFIER | c.777+5597delT | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160350415 | ||||||
chr3:160350415
|
CAA | C | 40 | a0001c0001t0001g0006a0001c0001t0001g0168a0001c0001t0001g0169others(37): Show | 41 | HG00323.hp2 HG00423.hp1 HG00642.hp2 others(38): Show |
intron_variant | MODIFIER | c.777+5596_777+5597d others(4): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160350415 | ||||||
chr3:160350690
|
G | T | 1 | a0002c0006t0002g0014 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.777+5323C>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160350690 | ||||||
chr3:160351017
|
T | C | 1 | a0001c0001t0001g0192 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.777+4996A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160351017 | ||||||
chr3:160351575
|
ATATAT | A | 28 | a0002c0002t0001g0046a0002c0002t0001g0047a0002c0002t0001g0056others(25): Show | 28 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(25): Show |
intron_variant | MODIFIER | c.777+4433_777+4437d others(7): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160351575 | ||||||
chr3:160351628
|
T | C | 3 | a0002c0003t0002g0079a0002c0003t0002g0080a0002c0003t0002g0081 | 3 | HG00738.hp2 HG01167.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.777+4385A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160351628 | ||||||
chr3:160351693
|
CATAAAAA others(40): Show |
C | 19 | a0002c0002t0002g0004a0002c0002t0002g0021a0002c0002t0002g0022others(16): Show | 20 | HG01069.hp2 HG01255.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.777+4273_777+4319d others(49): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160351693 | ||||||
chr3:160351740
|
T | C | 1 | a0002c0002t0001g0063 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.777+4273A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160351740 | ||||||
chr3:160352017
|
AT | A | 43 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(40): Show | 46 | HG00099.hp2 HG01069.hp2 HG01243.hp1 others(43): Show |
intron_variant | MODIFIER | c.777+3995delA | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160352017 | ||||||
chr3:160352276
|
G | A | 39 | a0001c0001t0001g0006a0001c0001t0001g0168a0001c0001t0001g0169others(36): Show | 40 | HG00323.hp2 HG00423.hp1 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.777+3737C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160352276 | ||||||
chr3:160352290
|
G | A | 1 | a0001c0001t0001g0113 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.777+3723C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160352290 | ||||||
chr3:160352725
|
G | C | 1 | a0002c0006t0002g0014 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.777+3288C>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160352725 | ||||||
chr3:160352994
|
C | T | 7 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(4): Show | 7 | HG00099.hp2 HG02976.hp1 HG03834.hp1 others(4): Show |
intron_variant | MODIFIER | c.777+3019G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160352994 | ||||||
chr3:160353119
|
A | T | 170 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(167): Show | 175 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(172): Show |
intron_variant | MODIFIER | c.777+2894T>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160353119 | ||||||
chr3:160353184
|
T | C | 1 | a0001c0001t0001g0136 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.777+2829A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160353184 | ||||||
chr3:160353233
|
A | G | 1 | a0002c0002t0002g0015 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.777+2780T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160353233 | ||||||
chr3:160353240
|
A | G | 6 | a0002c0002t0004g0018a0002c0002t0004g0019a0002c0002t0004g0020others(3): Show | 6 | HG02976.hp2 NA18960.hp1 NA18983.hp2 others(3): Show |
intron_variant | MODIFIER | c.777+2773T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160353240 | ||||||
chr3:160353489
|
A | G | 4 | a0002c0002t0002g0157a0002c0002t0002g0158a0002c0002t0002g0159others(1): Show | 4 | HG01167.hp2 HG01169.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.777+2524T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160353489 | ||||||
chr3:160353505
|
A | G | 1 | a0002c0002t0001g0066 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.777+2508T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160353505 | ||||||
chr3:160353520
|
T | C | 1 | a0002c0003t0008g0045 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.777+2493A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160353520 | ||||||
chr3:160353598
|
C | T | 1 | a0002c0003t0008g0045 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.777+2415G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160353598 | ||||||
chr3:160353630
|
C | T | 81 | a0001c0001t0001g0006a0001c0001t0001g0168a0001c0001t0001g0169others(78): Show | 82 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(79): Show |
intron_variant | MODIFIER | c.777+2383G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160353630 | ||||||
chr3:160354232
|
T | G | 24 | a0002c0002t0001g0046a0002c0002t0001g0047a0002c0002t0001g0056others(21): Show | 24 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(21): Show |
intron_variant | MODIFIER | c.777+1781A>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160354232 | ||||||
chr3:160354273
|
A | G | 1 | a0002c0006t0002g0014 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.777+1740T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160354273 | ||||||
chr3:160354477
|
G | A | 1 | a0001c0001t0001g0134 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.777+1536C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160354477 | ||||||
chr3:160354590
|
C | T | 125 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(122): Show | 129 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(126): Show |
intron_variant | MODIFIER | c.777+1423G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160354590 | ||||||
chr3:160354661
|
AT | A | 5 | a0002c0003t0002g0050a0002c0003t0002g0051a0002c0003t0002g0052others(2): Show | 5 | HG01891.hp2 HG02630.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.777+1351delA | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160354661 | ||||||
chr3:160355090
|
G | A | 15 | a0002c0002t0001g0033a0002c0002t0002g0003a0002c0002t0002g0032others(12): Show | 17 | HG01243.hp1 HG02451.hp2 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.777+923C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160355090 | ||||||
chr3:160355249
|
G | GTTAT | 3 | a0001c0001t0001g0168a0001c0001t0001g0175a0001c0001t0001g0178 | 3 | HG00642.hp2 HG01891.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.777+760_777+763dup others(4): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160355249 | ||||||
chr3:160355480
|
G | A | 1 | a0002c0002t0001g0072 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.777+533C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160355480 | ||||||
chr3:160355603
|
C | T | 43 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(40): Show | 46 | HG00099.hp2 HG01069.hp2 HG01243.hp1 others(43): Show |
intron_variant | MODIFIER | c.777+410G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160355603 | ||||||
chr3:160355743
|
A | G | 6 | a0002c0002t0004g0018a0002c0002t0004g0019a0002c0002t0004g0020others(3): Show | 6 | HG02976.hp2 NA18960.hp1 NA18983.hp2 others(3): Show |
intron_variant | MODIFIER | c.777+270T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160355743 | ||||||
chr3:160355993
|
T | C | 1 | a0002c0002t0001g0056 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.777+20A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160355993 | ||||||
chr3:160356208
|
A | G | 1 | a0002c0002t0002g0015 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.640-58T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 7/19 | chr3 | 160356208 | ||||||
chr3:160356417
|
T | C | 21 | a0002c0002t0002g0004a0002c0002t0002g0021a0002c0002t0002g0022others(18): Show | 22 | HG01069.hp2 HG01255.hp2 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.640-267A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 7/19 | chr3 | 160356417 | ||||||
chr3:160356512
|
T | C | 1 | a0001c0001t0001g0135 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.640-362A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 7/19 | chr3 | 160356512 | ||||||
chr3:160356796
|
T | C | 1 | a0002c0006t0002g0014 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.640-646A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 7/19 | chr3 | 160356796 | ||||||
chr3:160356979
|
A | G | 81 | a0001c0001t0001g0006a0001c0001t0001g0168a0001c0001t0001g0169others(78): Show | 82 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(79): Show |
intron_variant | MODIFIER | c.639+510T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 7/19 | chr3 | 160356979 | ||||||
chr3:160357259
|
C | A | 1 | a0002c0003t0002g0052 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.639+230G>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 7/19 | chr3 | 160357259 | ||||||
chr3:160357318
|
G | A | 1 | a0001c0001t0001g0144 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.639+171C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 7/19 | chr3 | 160357318 | ||||||
chr3:160357768
|
C | T | 1 | a0001c0001t0001g0189 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.550-190G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 6/19 | chr3 | 160357768 | ||||||
chr3:160357868
|
G | A | 1 | a0001c0001t0001g0136 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.550-290C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 6/19 | chr3 | 160357868 | ||||||
chr3:160357995
|
CTTAT | C | 7 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(4): Show | 7 | HG00099.hp2 HG02976.hp1 HG03834.hp1 others(4): Show |
intron_variant | MODIFIER | c.550-421_550-418del others(4): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 6/19 | chr3 | 160357995 | ||||||
chr3:160358156
|
T | C | 20 | a0002c0002t0002g0004a0002c0002t0002g0021a0002c0002t0002g0022others(17): Show | 21 | HG01069.hp2 HG01255.hp2 HG02055.hp1 others(18): Show |
intron_variant | MODIFIER | c.550-578A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 6/19 | chr3 | 160358156 | ||||||
chr3:160358248
|
A | G | 1 | a0001c0001t0001g0147 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.550-670T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 6/19 | chr3 | 160358248 | ||||||
chr3:160358292
|
C | T | 1 | a0002c0002t0002g0015 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.550-714G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 6/19 | chr3 | 160358292 | ||||||
chr3:160358293
|
G | A | 4 | a0002c0002t0002g0022a0002c0002t0002g0023a0002c0002t0002g0024others(1): Show | 4 | HG02280.hp2 HG02451.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.550-715C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 6/19 | chr3 | 160358293 | ||||||
chr3:160359208
|
C | T | 1 | a0002c0002t0002g0055 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.550-1630G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 6/19 | chr3 | 160359208 | ||||||
chr3:160359257
|
G | A | 1 | a0002c0002t0002g0015 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.550-1679C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 6/19 | chr3 | 160359257 | ||||||
chr3:160359410
|
G | A | 1 | a0002c0002t0007g0088 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.550-1832C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 6/19 | chr3 | 160359410 | ||||||
chr3:160359550
|
C | T | 1 | a0001c0001t0001g0104 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.550-1972G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 6/19 | chr3 | 160359550 | ||||||
chr3:160359558
|
C | A | 1 | a0001c0001t0001g0136 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.550-1980G>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 6/19 | chr3 | 160359558 | ||||||
chr3:160359856
|
A | T | 39 | a0001c0001t0001g0006a0001c0001t0001g0168a0001c0001t0001g0169others(36): Show | 40 | HG00323.hp2 HG00423.hp1 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.550-2278T>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 6/19 | chr3 | 160359856 | ||||||
chr3:160360018
|
A | G | 5 | a0002c0002t0002g0156a0002c0002t0002g0157a0002c0002t0002g0158others(2): Show | 5 | HG01167.hp2 HG01169.hp1 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.550-2440T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 6/19 | chr3 | 160360018 | ||||||
chr3:160360058
|
A | G | 135 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(132): Show | 140 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(137): Show |
intron_variant | MODIFIER | c.550-2480T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 6/19 | chr3 | 160360058 | ||||||
chr3:160360145
|
G | A | 1 | a0005c0007t0001g0137 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.550-2567C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 6/19 | chr3 | 160360145 | ||||||
chr3:160360155
|
C | G | 81 | a0001c0001t0001g0006a0001c0001t0001g0168a0001c0001t0001g0169others(78): Show | 82 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(79): Show |
intron_variant | MODIFIER | c.550-2577G>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 6/19 | chr3 | 160360155 | ||||||
chr3:160360353
|
A | G | 1 | a0002c0002t0002g0037 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.550-2775T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 6/19 | chr3 | 160360353 | ||||||
chr3:160360954
|
A | G | 1 | a0002c0002t0002g0015 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.550-3376T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 6/19 | chr3 | 160360954 | ||||||
chr3:160360991
|
G | A | 1 | a0002c0002t0001g0067 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.550-3413C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 6/19 | chr3 | 160360991 | ||||||
chr3:160361002
|
G | A | 1 | a0002c0002t0003g0039 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.550-3424C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 6/19 | chr3 | 160361002 | ||||||
chr3:160361086
|
T | C | 81 | a0001c0001t0001g0006a0001c0001t0001g0168a0001c0001t0001g0169others(78): Show | 82 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(79): Show |
intron_variant | MODIFIER | c.550-3508A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 6/19 | chr3 | 160361086 | ||||||
chr3:160361443
|
T | C | 1 | a0001c0001t0001g0111 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.550-3865A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 6/19 | chr3 | 160361443 | ||||||
chr3:160361498
|
C | A | 1 | a0001c0001t0001g0146 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.550-3920G>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 6/19 | chr3 | 160361498 | ||||||
chr3:160361613
|
C | T | 1 | a0002c0002t0002g0055 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.550-4035G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 6/19 | chr3 | 160361613 | ||||||
chr3:160361617
|
T | C | 1 | a0002c0002t0002g0015 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.550-4039A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 6/19 | chr3 | 160361617 | ||||||
chr3:160361740
|
C | A | 2 | a0001c0001t0001g0010a0001c0001t0001g0011 | 2 | NA18944.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.550-4162G>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 6/19 | chr3 | 160361740 | ||||||
chr3:160361759
|
C | T | 3 | a0002c0003t0002g0079a0002c0003t0002g0080a0002c0003t0002g0081 | 3 | HG00738.hp2 HG01167.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.550-4181G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 6/19 | chr3 | 160361759 | ||||||
chr3:160363016
|
C | T | 21 | a0002c0002t0002g0004a0002c0002t0002g0021a0002c0002t0002g0022others(18): Show | 22 | HG01069.hp2 HG01255.hp2 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.549+3027G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 6/19 | chr3 | 160363016 | ||||||
chr3:160363031
|
G | C | 8 | a0002c0002t0002g0021a0002c0002t0002g0022a0002c0002t0002g0023others(5): Show | 8 | HG01255.hp2 HG02055.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.549+3012C>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 6/19 | chr3 | 160363031 | ||||||
chr3:160363123
|
T | C | 1 | a0002c0002t0003g0030 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.549+2920A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 6/19 | chr3 | 160363123 | ||||||
chr3:160363192
|
G | A | 1 | a0002c0002t0002g0049 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.549+2851C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 6/19 | chr3 | 160363192 | ||||||
chr3:160363401
|
G | C | 43 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(40): Show | 46 | HG00099.hp2 HG01069.hp2 HG01243.hp1 others(43): Show |
intron_variant | MODIFIER | c.549+2642C>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 6/19 | chr3 | 160363401 | ||||||
chr3:160363866
|
G | T | 1 | a0001c0008t0001g0164 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.549+2177C>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 6/19 | chr3 | 160363866 | ||||||
chr3:160363911
|
G | A | 1 | a0001c0001t0001g0103 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.549+2132C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 6/19 | chr3 | 160363911 | ||||||
chr3:160364071
|
C | T | 1 | a0003c0004t0002g0027 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.549+1972G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 6/19 | chr3 | 160364071 | ||||||
chr3:160364283
|
T | C | 126 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(123): Show | 130 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(127): Show |
intron_variant | MODIFIER | c.549+1760A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 6/19 | chr3 | 160364283 | ||||||
chr3:160364293
|
C | G | 1 | a0002c0002t0002g0015 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.549+1750G>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 6/19 | chr3 | 160364293 | ||||||
chr3:160364366
|
A | G | 126 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(123): Show | 130 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(127): Show |
intron_variant | MODIFIER | c.549+1677T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 6/19 | chr3 | 160364366 | ||||||
chr3:160364496
|
T | C | 81 | a0001c0001t0001g0006a0001c0001t0001g0168a0001c0001t0001g0169others(78): Show | 82 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(79): Show |
intron_variant | MODIFIER | c.549+1547A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 6/19 | chr3 | 160364496 | ||||||
chr3:160364589
|
C | G | 3 | a0001c0001t0001g0116a0001c0001t0001g0117a0001c0001t0001g0118 | 3 | HG01981.hp2 HG03490.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.549+1454G>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 6/19 | chr3 | 160364589 | ||||||
chr3:160364885
|
G | A | 2 | a0002c0002t0002g0004a0002c0002t0002g0028 | 3 | HG02886.hp2 HG03225.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.549+1158C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 6/19 | chr3 | 160364885 | ||||||
chr3:160365002
|
T | TA | 38 | a0001c0001t0001g0006a0001c0001t0001g0168a0001c0001t0001g0169others(35): Show | 39 | HG00323.hp2 HG00642.hp2 HG00735.hp2 others(36): Show |
intron_variant | MODIFIER | c.549+1040dupT | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 6/19 | chr3 | 160365002 | ||||||
chr3:160365013
|
GA | G | 43 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(40): Show | 46 | HG00099.hp2 HG01069.hp2 HG01243.hp1 others(43): Show |
intron_variant | MODIFIER | c.549+1029delT | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 6/19 | chr3 | 160365013 | ||||||
chr3:160365712
|
G | T | 2 | a0002c0002t0002g0048a0002c0002t0002g0082 | 2 | HG01069.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.549+331C>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 6/19 | chr3 | 160365712 | ||||||
chr3:160365793
|
C | T | 2 | a0001c0001t0001g0115a0002c0002t0002g0015 | 2 | HG00741.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.549+250G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 6/19 | chr3 | 160365793 | ||||||
chr3:160365997
|
C | T | 1 | a0002c0002t0002g0055 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.549+46G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 6/19 | chr3 | 160365997 | ||||||
chr3:160366027
|
A | G | 1 | a0001c0001t0010g0114 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.549+16T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 6/19 | chr3 | 160366027 | ||||||
chr3:160366278
|
T | C | 1 | a0001c0001t0001g0008 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.440-126A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 5/19 | chr3 | 160366278 | ||||||
chr3:160366786
|
T | C | 1 | a0001c0001t0001g0138 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.440-634A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 5/19 | chr3 | 160366786 | ||||||
chr3:160367084
|
T | C | 3 | a0002c0002t0002g0202a0002c0002t0002g0203a0002c0002t0002g0205 | 3 | HG02965.hp2 HG03130.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.440-932A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 5/19 | chr3 | 160367084 | ||||||
chr3:160367112
|
AT | A | 5 | a0002c0002t0002g0156a0002c0002t0002g0157a0002c0002t0002g0158others(2): Show | 5 | HG01167.hp2 HG01169.hp1 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.440-961delA | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 5/19 | chr3 | 160367112 | ||||||
chr3:160367500
|
C | T | 6 | a0002c0003t0002g0050a0002c0003t0002g0051a0002c0003t0002g0052others(3): Show | 6 | HG01891.hp2 HG02630.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.440-1348G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 5/19 | chr3 | 160367500 | ||||||
chr3:160367613
|
A | G | 6 | a0002c0002t0004g0018a0002c0002t0004g0019a0002c0002t0004g0020others(3): Show | 6 | HG02976.hp2 NA18960.hp1 NA18983.hp2 others(3): Show |
intron_variant | MODIFIER | c.440-1461T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 5/19 | chr3 | 160367613 | ||||||
chr3:160367860
|
T | C | 1 | a0002c0002t0002g0015 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.440-1708A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 5/19 | chr3 | 160367860 | ||||||
chr3:160367878
|
C | T | 1 | a0002c0002t0002g0015 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.440-1726G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 5/19 | chr3 | 160367878 | ||||||
chr3:160368215
|
G | T | 1 | a0001c0001t0001g0094 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.440-2063C>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 5/19 | chr3 | 160368215 | ||||||
chr3:160368267
|
G | T | 125 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(122): Show | 129 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(126): Show |
intron_variant | MODIFIER | c.440-2115C>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 5/19 | chr3 | 160368267 | ||||||
chr3:160368359
|
C | CA | 10 | a0001c0001t0001g0094a0001c0001t0001g0104a0001c0001t0001g0139others(7): Show | 10 | HG00642.hp1 HG01106.hp1 HG02074.hp2 others(7): Show |
intron_variant | MODIFIER | c.440-2208dupT | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 5/19 | chr3 | 160368359 | ||||||
chr3:160368359
|
CA | C | 113 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(110): Show | 118 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(115): Show |
intron_variant | MODIFIER | c.440-2208delT | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 5/19 | chr3 | 160368359 | ||||||
chr3:160368359
|
CAA | C | 8 | a0001c0001t0001g0197a0002c0002t0001g0068a0002c0002t0002g0156others(5): Show | 8 | HG01167.hp2 HG01169.hp1 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.440-2209_440-2208d others(4): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 5/19 | chr3 | 160368359 | ||||||
chr3:160368518
|
T | C | 5 | a0002c0002t0002g0156a0002c0002t0002g0157a0002c0002t0002g0158others(2): Show | 5 | HG01167.hp2 HG01169.hp1 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.440-2366A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 5/19 | chr3 | 160368518 | ||||||
chr3:160368649
|
G | A | 1 | a0001c0001t0001g0150 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.440-2497C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 5/19 | chr3 | 160368649 | ||||||
chr3:160368713
|
C | T | 23 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(20): Show | 25 | HG00099.hp2 HG01243.hp1 HG02451.hp2 others(22): Show |
intron_variant | MODIFIER | c.440-2561G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 5/19 | chr3 | 160368713 | ||||||
chr3:160368796
|
A | AAT | 126 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(123): Show | 130 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(127): Show |
intron_variant | MODIFIER | c.440-2646_440-2645d others(4): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 5/19 | chr3 | 160368796 | ||||||
chr3:160368875
|
G | A | 1 | a0002c0002t0002g0083 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.440-2723C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 5/19 | chr3 | 160368875 | ||||||
chr3:160368930
|
T | TA | 2 | a0002c0002t0001g0084a0002c0002t0001g0085 | 2 | HG02602.hp1 HG03490.hp2 |
intron_variant | MODIFIER | c.440-2779dupT | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 5/19 | chr3 | 160368930 | ||||||
chr3:160369005
|
C | T | 21 | a0002c0002t0002g0004a0002c0002t0002g0021a0002c0002t0002g0022others(18): Show | 22 | HG01069.hp2 HG01255.hp2 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.440-2853G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 5/19 | chr3 | 160369005 | ||||||
chr3:160369262
|
A | T | 1 | a0001c0001t0001g0108 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.440-3110T>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 5/19 | chr3 | 160369262 | ||||||
chr3:160369463
|
C | T | 1 | a0002c0002t0002g0055 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.440-3311G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 5/19 | chr3 | 160369463 | ||||||
chr3:160369832
|
T | G | 1 | a0002c0002t0003g0040 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.440-3680A>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 5/19 | chr3 | 160369832 | ||||||
chr3:160369965
|
G | A | 1 | a0002c0002t0004g0019 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.440-3813C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 5/19 | chr3 | 160369965 | ||||||
chr3:160370144
|
C | T | 1 | a0001c0001t0001g0113 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.440-3992G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 5/19 | chr3 | 160370144 | ||||||
chr3:160370243
|
A | C | 5 | a0001c0001t0001g0096a0001c0001t0001g0097a0001c0001t0001g0098others(2): Show | 5 | HG02258.hp1 HG02809.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.440-4091T>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 5/19 | chr3 | 160370243 | ||||||
chr3:160370359
|
T | C | 1 | a0002c0003t0002g0053 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.440-4207A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 5/19 | chr3 | 160370359 | ||||||
chr3:160370375
|
A | AT | 28 | a0001c0001t0001g0112a0001c0001t0001g0168a0001c0001t0001g0169others(25): Show | 28 | HG00323.hp2 HG00642.hp2 HG00735.hp2 others(25): Show |
intron_variant | MODIFIER | c.440-4224dupA | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 5/19 | chr3 | 160370375 | ||||||
chr3:160370375
|
A | ATT | 11 | a0001c0001t0001g0006a0001c0001t0001g0171a0001c0001t0001g0189others(8): Show | 12 | HG00423.hp1 HG01433.hp2 HG01952.hp1 others(9): Show |
intron_variant | MODIFIER | c.440-4225_440-4224d others(4): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 5/19 | chr3 | 160370375 | ||||||
chr3:160370420
|
C | T | 1 | a0001c0001t0001g0188 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.440-4268G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 5/19 | chr3 | 160370420 | ||||||
chr3:160370561
|
A | AT | 43 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(40): Show | 46 | HG00099.hp2 HG01069.hp2 HG01243.hp1 others(43): Show |
intron_variant | MODIFIER | c.440-4410dupA | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 5/19 | chr3 | 160370561 | ||||||
chr3:160370651
|
C | T | 4 | a0002c0002t0001g0033a0002c0002t0002g0003a0002c0002t0002g0034others(1): Show | 5 | HG01243.hp1 HG02723.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.440-4499G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 5/19 | chr3 | 160370651 | ||||||
chr3:160370965
|
A | G | 3 | a0002c0003t0002g0079a0002c0003t0002g0080a0002c0003t0002g0081 | 3 | HG00738.hp2 HG01167.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.440-4813T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 5/19 | chr3 | 160370965 | ||||||
chr3:160371013
|
T | C | 1 | a0001c0001t0001g0007 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.439+4799A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 5/19 | chr3 | 160371013 | ||||||
chr3:160371248
|
A | C | 5 | a0002c0002t0002g0156a0002c0002t0002g0157a0002c0002t0002g0158others(2): Show | 5 | HG01167.hp2 HG01169.hp1 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.439+4564T>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 5/19 | chr3 | 160371248 | ||||||
chr3:160371253
|
C | T | 1 | a0002c0002t0002g0015 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.439+4559G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 5/19 | chr3 | 160371253 | ||||||
chr3:160371363
|
C | G | 7 | a0001c0001t0001g0170a0001c0001t0001g0174a0001c0001t0001g0176others(4): Show | 7 | HG00735.hp2 HG01070.hp2 HG01109.hp2 others(4): Show |
intron_variant | MODIFIER | c.439+4449G>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 5/19 | chr3 | 160371363 | ||||||
chr3:160371633
|
G | T | 1 | a0002c0002t0002g0055 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.439+4179C>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 5/19 | chr3 | 160371633 | ||||||
chr3:160371660
|
C | A | 1 | a0002c0002t0002g0055 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.439+4152G>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 5/19 | chr3 | 160371660 | ||||||
chr3:160371944
|
T | C | 1 | a0001c0001t0001g0108 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.439+3868A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 5/19 | chr3 | 160371944 | ||||||
chr3:160372029
|
C | T | 1 | a0001c0001t0001g0161 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.439+3783G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 5/19 | chr3 | 160372029 | ||||||
chr3:160372108
|
G | A | 43 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(40): Show | 46 | HG00099.hp2 HG01069.hp2 HG01243.hp1 others(43): Show |
intron_variant | MODIFIER | c.439+3704C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 5/19 | chr3 | 160372108 | ||||||
chr3:160372206
|
C | T | 1 | a0001c0001t0001g0111 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.439+3606G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 5/19 | chr3 | 160372206 | ||||||
chr3:160372246
|
T | C | 19 | a0002c0002t0002g0004a0002c0002t0002g0021a0002c0002t0002g0022others(16): Show | 20 | HG01069.hp2 HG01255.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.439+3566A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 5/19 | chr3 | 160372246 | ||||||
chr3:160372290
|
G | C | 1 | a0001c0001t0006g0198 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.439+3522C>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 5/19 | chr3 | 160372290 | ||||||
chr3:160372702
|
T | C | 21 | a0002c0002t0002g0004a0002c0002t0002g0021a0002c0002t0002g0022others(18): Show | 22 | HG01069.hp2 HG01255.hp2 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.439+3110A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 5/19 | chr3 | 160372702 | ||||||
chr3:160373189
|
T | C | 7 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(4): Show | 7 | HG00099.hp2 HG02976.hp1 HG03834.hp1 others(4): Show |
intron_variant | MODIFIER | c.439+2623A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 5/19 | chr3 | 160373189 | ||||||
chr3:160373197
|
G | A | 15 | a0002c0002t0001g0033a0002c0002t0002g0003a0002c0002t0002g0032others(12): Show | 17 | HG01243.hp1 HG02451.hp2 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.439+2615C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 5/19 | chr3 | 160373197 | ||||||
chr3:160373578
|
A | G | 1 | a0001c0001t0001g0013 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.439+2234T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 5/19 | chr3 | 160373578 | ||||||
chr3:160373772
|
A | T | 1 | a0002c0002t0002g0037 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.439+2040T>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 5/19 | chr3 | 160373772 | ||||||
chr3:160373913
|
C | T | 15 | a0002c0002t0001g0033a0002c0002t0002g0003a0002c0002t0002g0032others(12): Show | 17 | HG01243.hp1 HG02451.hp2 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.439+1899G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 5/19 | chr3 | 160373913 | ||||||
chr3:160373920
|
C | G | 22 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(19): Show | 24 | HG00099.hp2 HG01243.hp1 HG02451.hp2 others(21): Show |
intron_variant | MODIFIER | c.439+1892G>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 5/19 | chr3 | 160373920 | ||||||
chr3:160374323
|
C | T | 1 | a0001c0001t0001g0007 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.439+1489G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 5/19 | chr3 | 160374323 | ||||||
chr3:160374366
|
G | A | 1 | a0001c0008t0001g0164 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.439+1446C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 5/19 | chr3 | 160374366 | ||||||
chr3:160374713
|
T | C | 5 | a0002c0003t0002g0050a0002c0003t0002g0051a0002c0003t0002g0052others(2): Show | 5 | HG01891.hp2 HG02630.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.439+1099A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 5/19 | chr3 | 160374713 | ||||||
chr3:160374781
|
C | T | 2 | a0003c0004t0002g0026a0003c0004t0002g0027 | 2 | HG01255.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.439+1031G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 5/19 | chr3 | 160374781 | ||||||
chr3:160374838
|
G | A | 1 | a0002c0006t0002g0014 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.439+974C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 5/19 | chr3 | 160374838 | ||||||
chr3:160375010
|
C | T | 39 | a0001c0001t0001g0006a0001c0001t0001g0168a0001c0001t0001g0169others(36): Show | 40 | HG00323.hp2 HG00423.hp1 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.439+802G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 5/19 | chr3 | 160375010 | ||||||
chr3:160375497
|
T | A | 15 | a0002c0002t0001g0033a0002c0002t0002g0003a0002c0002t0002g0032others(12): Show | 17 | HG01243.hp1 HG02451.hp2 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.439+315A>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 5/19 | chr3 | 160375497 | ||||||
chr3:160375647
|
A | G | 1 | a0001c0001t0001g0110 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.439+165T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 5/19 | chr3 | 160375647 | ||||||
chr3:160375726
|
G | A | 1 | a0002c0002t0001g0072 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.439+86C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 5/19 | chr3 | 160375726 | ||||||
chr3:160375890
|
G | T | 1 | a0001c0001t0001g0109 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.371-10C>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 4/19 | chr3 | 160375890 | ||||||
chr3:160375973
|
G | A | 1 | a0001c0001t0001g0094 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.371-93C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 4/19 | chr3 | 160375973 | ||||||
chr3:160376104
|
C | T | 8 | a0002c0002t0002g0021a0002c0002t0002g0022a0002c0002t0002g0023others(5): Show | 8 | HG01255.hp2 HG02055.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.371-224G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 4/19 | chr3 | 160376104 | ||||||
chr3:160376247
|
A | C | 1 | a0001c0001t0001g0106 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.371-367T>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 4/19 | chr3 | 160376247 | ||||||
chr3:160376356
|
AG | A | 7 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(4): Show | 7 | HG00099.hp2 HG02976.hp1 HG03834.hp1 others(4): Show |
intron_variant | MODIFIER | c.371-477delC | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 4/19 | chr3 | 160376356 | ||||||
chr3:160377199
|
G | A | 2 | a0001c0001t0001g0008a0001c0001t0001g0009 | 2 | HG00099.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.370+231C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 4/19 | chr3 | 160377199 | ||||||
chr3:160377232
|
G | T | 22 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(19): Show | 24 | HG00099.hp2 HG01243.hp1 HG02451.hp2 others(21): Show |
intron_variant | MODIFIER | c.370+198C>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 4/19 | chr3 | 160377232 | ||||||
chr3:160377351
|
C | T | 1 | a0001c0001t0001g0094 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.370+79G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 4/19 | chr3 | 160377351 | ||||||
chr3:160377356
|
T | C | 15 | a0002c0002t0001g0033a0002c0002t0002g0003a0002c0002t0002g0032others(12): Show | 17 | HG01243.hp1 HG02451.hp2 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.370+74A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 4/19 | chr3 | 160377356 | ||||||
chr3:160377658
|
C | T | 1 | a0002c0002t0002g0015 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.260-118G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 3/19 | chr3 | 160377658 | ||||||
chr3:160378240
|
T | TA | 11 | a0002c0002t0002g0037a0002c0002t0002g0055a0002c0002t0002g0202others(8): Show | 12 | HG02451.hp2 HG02486.hp2 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.260-701dupT | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 3/19 | chr3 | 160378240 | ||||||
chr3:160378567
|
A | C | 43 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(40): Show | 46 | HG00099.hp2 HG01069.hp2 HG01243.hp1 others(43): Show |
intron_variant | MODIFIER | c.260-1027T>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 3/19 | chr3 | 160378567 | ||||||
chr3:160378646
|
T | A | 7 | a0001c0001t0001g0144a0002c0002t0002g0021a0002c0002t0002g0022others(4): Show | 7 | HG02055.hp1 HG02280.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.260-1106A>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 3/19 | chr3 | 160378646 | ||||||
chr3:160378833
|
G | A | 1 | a0001c0001t0001g0145 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.260-1293C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 3/19 | chr3 | 160378833 | ||||||
chr3:160378847
|
A | T | 1 | a0001c0001t0001g0108 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.260-1307T>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 3/19 | chr3 | 160378847 | ||||||
chr3:160378854
|
A | G | 5 | a0002c0003t0002g0050a0002c0003t0002g0051a0002c0003t0002g0052others(2): Show | 5 | HG01891.hp2 HG02630.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.260-1314T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 3/19 | chr3 | 160378854 | ||||||
chr3:160379318
|
T | C | 1 | a0002c0002t0002g0173 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.260-1778A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 3/19 | chr3 | 160379318 | ||||||
chr3:160379560
|
G | A | 1 | a0002c0002t0002g0055 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.259+1943C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 3/19 | chr3 | 160379560 | ||||||
chr3:160379691
|
T | G | 1 | a0001c0001t0001g0188 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.259+1812A>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 3/19 | chr3 | 160379691 | ||||||
chr3:160380007
|
G | A | 21 | a0002c0002t0002g0004a0002c0002t0002g0021a0002c0002t0002g0022others(18): Show | 22 | HG01069.hp2 HG01255.hp2 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.259+1496C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 3/19 | chr3 | 160380007 | ||||||
chr3:160380036
|
CT | C | 125 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(122): Show | 129 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(126): Show |
intron_variant | MODIFIER | c.259+1466delA | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 3/19 | chr3 | 160380036 | ||||||
chr3:160380094
|
G | A | 1 | a0002c0006t0002g0014 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.259+1409C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 3/19 | chr3 | 160380094 | ||||||
chr3:160380125
|
C | G | 1 | a0001c0001t0001g0107 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.259+1378G>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 3/19 | chr3 | 160380125 | ||||||
chr3:160380128
|
G | A | 6 | a0002c0002t0001g0058a0002c0002t0001g0059a0002c0002t0001g0062others(3): Show | 6 | HG00423.hp2 HG00558.hp2 NA18942.hp1 others(3): Show |
intron_variant | MODIFIER | c.259+1375C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 3/19 | chr3 | 160380128 | ||||||
chr3:160380200
|
A | T | 1 | a0001c0001t0001g0106 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.259+1303T>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 3/19 | chr3 | 160380200 | ||||||
chr3:160380241
|
T | C | 1 | a0001c0001t0001g0166 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.259+1262A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 3/19 | chr3 | 160380241 | ||||||
chr3:160380537
|
C | T | 5 | a0002c0002t0004g0018a0002c0002t0004g0019a0002c0002t0004g0020others(2): Show | 5 | NA18960.hp1 NA18983.hp2 NA18990.hp1 others(2): Show |
intron_variant | MODIFIER | c.259+966G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 3/19 | chr3 | 160380537 | ||||||
chr3:160380549
|
G | A | 2 | a0002c0002t0002g0032a0002c0002t0002g0036 | 2 | HG03139.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.259+954C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 3/19 | chr3 | 160380549 | ||||||
chr3:160380705
|
GT | G | 3 | a0002c0002t0001g0076a0002c0002t0001g0077a0002c0002t0001g0078 | 3 | HG02622.hp1 HG02818.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.259+797delA | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 3/19 | chr3 | 160380705 | ||||||
chr3:160380707
|
G | GA | 28 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(25): Show | 29 | HG00099.hp2 HG01069.hp2 HG01255.hp2 others(26): Show |
intron_variant | MODIFIER | c.259+795dupT | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 3/19 | chr3 | 160380707 | ||||||
chr3:160380708
|
A | G | 3 | a0002c0002t0001g0076a0002c0002t0001g0077a0002c0002t0001g0078 | 3 | HG02622.hp1 HG02818.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.259+795T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 3/19 | chr3 | 160380708 | ||||||
chr3:160380749
|
C | T | 39 | a0001c0001t0001g0006a0001c0001t0001g0168a0001c0001t0001g0169others(36): Show | 40 | HG00323.hp2 HG00423.hp1 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.259+754G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 3/19 | chr3 | 160380749 | ||||||
chr3:160380902
|
A | C | 1 | a0002c0002t0002g0055 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.259+601T>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 3/19 | chr3 | 160380902 | ||||||
chr3:160380927
|
C | G | 1 | a0002c0003t0008g0045 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.259+576G>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 3/19 | chr3 | 160380927 | ||||||
chr3:160380975
|
C | T | 22 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(19): Show | 24 | HG00099.hp2 HG01243.hp1 HG02451.hp2 others(21): Show |
intron_variant | MODIFIER | c.259+528G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 3/19 | chr3 | 160380975 | ||||||
chr3:160381010
|
A | G | 1 | a0002c0002t0002g0015 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.259+493T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 3/19 | chr3 | 160381010 | ||||||
chr3:160381071
|
C | CA | 6 | a0002c0002t0004g0018a0002c0002t0004g0019a0002c0002t0004g0020others(3): Show | 6 | HG02976.hp2 NA18960.hp1 NA18983.hp2 others(3): Show |
intron_variant | MODIFIER | c.259+431dupT | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 3/19 | chr3 | 160381071 | ||||||
chr3:160381080
|
T | G | 6 | a0002c0002t0004g0018a0002c0002t0004g0019a0002c0002t0004g0020others(3): Show | 6 | HG02976.hp2 NA18960.hp1 NA18983.hp2 others(3): Show |
intron_variant | MODIFIER | c.259+423A>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 3/19 | chr3 | 160381080 | ||||||
chr3:160381227
|
A | G | 1 | a0001c0001t0001g0105 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.259+276T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 3/19 | chr3 | 160381227 | ||||||
chr3:160381231
|
C | A | 1 | a0001c0001t0001g0174 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.259+272G>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 3/19 | chr3 | 160381231 | ||||||
chr3:160381239
|
A | AAT | 21 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0001g0100others(18): Show | 23 | HG01106.hp1 HG01168.hp2 HG01243.hp1 others(20): Show |
intron_variant | MODIFIER | c.259+262_259+263dup others(2): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 3/19 | chr3 | 160381239 | ||||||
chr3:160381239
|
A | AATAT | 17 | a0002c0002t0002g0004a0002c0002t0002g0021a0002c0002t0002g0022others(14): Show | 18 | HG01069.hp2 HG01255.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.259+260_259+263dup others(4): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 3/19 | chr3 | 160381239 | ||||||
chr3:160381239
|
A | AATATATA others(1): Show |
9 | a0002c0002t0002g0048a0002c0002t0004g0018a0002c0002t0004g0019others(6): Show | 9 | HG00738.hp2 HG01167.hp1 HG01261.hp1 others(6): Show |
intron_variant | MODIFIER | c.259+256_259+263dup others(8): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 3/19 | chr3 | 160381239 | ||||||
chr3:160381239
|
A | AATATATA others(3): Show |
4 | a0002c0002t0001g0063a0002c0002t0001g0064a0002c0002t0001g0065others(1): Show | 4 | HG02257.hp1 HG03579.hp1 NA18942.hp1 others(1): Show |
intron_variant | MODIFIER | c.259+254_259+263dup others(10): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 3/19 | chr3 | 160381239 | ||||||
chr3:160381239
|
A | AATATATA others(5): Show |
12 | a0001c0001t0001g0170a0001c0001t0001g0174a0001c0001t0001g0176others(9): Show | 12 | HG00735.hp2 HG01109.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.259+252_259+263dup others(12): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 3/19 | chr3 | 160381239 | ||||||
chr3:160381239
|
A | AATATATA others(7): Show |
6 | a0001c0001t0001g0181a0001c0001t0001g0199a0002c0002t0001g0062others(3): Show | 6 | HG00423.hp2 HG01070.hp2 HG02074.hp1 others(3): Show |
intron_variant | MODIFIER | c.259+250_259+263dup others(14): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 3/19 | chr3 | 160381239 | ||||||
chr3:160381239
|
A | AATATATA others(9): Show |
8 | a0001c0001t0001g0180a0001c0001t0001g0195a0001c0001t0001g0196others(5): Show | 8 | HG00323.hp2 HG00423.hp1 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.259+248_259+263dup others(16): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 3/19 | chr3 | 160381239 | ||||||
chr3:160381239
|
A | AATATATA others(11): Show |
6 | a0001c0001t0001g0171a0001c0001t0001g0193a0001c0001t0001g0194others(3): Show | 6 | HG01433.hp2 HG01891.hp2 HG01981.hp1 others(3): Show |
intron_variant | MODIFIER | c.259+246_259+263dup others(18): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 3/19 | chr3 | 160381239 | ||||||
chr3:160381239
|
A | AATATATA others(13): Show |
7 | a0001c0001t0001g0006a0001c0001t0001g0168a0001c0001t0001g0175others(4): Show | 8 | HG00642.hp2 HG01891.hp1 HG01952.hp1 others(5): Show |
intron_variant | MODIFIER | c.259+244_259+263dup others(20): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 3/19 | chr3 | 160381239 | ||||||
chr3:160381239
|
A | AATATATA others(15): Show |
6 | a0001c0001t0001g0169a0001c0001t0001g0191a0002c0002t0002g0204others(3): Show | 6 | HG00738.hp1 HG02258.hp2 HG02523.hp2 others(3): Show |
intron_variant | MODIFIER | c.259+242_259+263dup others(22): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 3/19 | chr3 | 160381239 | ||||||
chr3:160381239
|
A | AATATATA others(17): Show |
4 | a0001c0001t0001g0178a0001c0001t0001g0190a0002c0002t0001g0061others(1): Show | 4 | HG01361.hp2 HG02293.hp1 HG03239.hp1 others(1): Show |
intron_variant | MODIFIER | c.259+240_259+263dup others(24): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 3/19 | chr3 | 160381239 | ||||||
chr3:160381239
|
A | AATATATA others(19): Show |
6 | a0001c0001t0001g0011a0002c0002t0001g0076a0002c0002t0002g0157others(3): Show | 6 | HG01167.hp2 HG01169.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.259+238_259+263dup others(26): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 3/19 | chr3 | 160381239 | ||||||
chr3:160381239
|
A | AATATATA others(21): Show |
5 | a0001c0001t0001g0009a0002c0002t0001g0060a0002c0002t0001g0070others(2): Show | 5 | HG00099.hp2 HG00735.hp1 HG00741.hp2 others(2): Show |
intron_variant | MODIFIER | c.259+263_259+264ins others(28): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 3/19 | chr3 | 160381239 | ||||||
chr3:160381239
|
A | AATATATA others(23): Show |
5 | a0001c0001t0001g0013a0001c0001t0001g0177a0002c0002t0001g0056others(2): Show | 5 | HG00280.hp1 HG01358.hp1 HG04115.hp2 others(2): Show |
intron_variant | MODIFIER | c.259+263_259+264ins others(30): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 3/19 | chr3 | 160381239 | ||||||
chr3:160381239
|
A | AATATATA others(25): Show |
3 | a0001c0001t0001g0008a0002c0002t0001g0084a0002c0002t0001g0085 | 3 | HG02602.hp1 HG03490.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.259+263_259+264ins others(32): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 3/19 | chr3 | 160381239 | ||||||
chr3:160381239
|
A | AATATATA others(27): Show |
4 | a0001c0001t0001g0010a0001c0001t0001g0012a0002c0002t0001g0057others(1): Show | 4 | HG00099.hp1 HG00558.hp2 NA18944.hp2 others(1): Show |
intron_variant | MODIFIER | c.259+263_259+264ins others(34): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 3/19 | chr3 | 160381239 | ||||||
chr3:160381239
|
A | AATATATA others(31): Show |
3 | a0002c0002t0001g0068a0002c0002t0001g0069a0002c0002t0001g0075 | 3 | HG00140.hp1 HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.259+263_259+264ins others(38): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 3/19 | chr3 | 160381239 | ||||||
chr3:160381239
|
A | AATATATA others(33): Show |
2 | a0001c0001t0001g0007a0002c0002t0001g0074 | 2 | HG01516.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.259+263_259+264ins others(40): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 3/19 | chr3 | 160381239 | ||||||
chr3:160381239
|
A | AATATATA others(35): Show |
1 | a0002c0002t0001g0073 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.259+263_259+264ins others(42): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 3/19 | chr3 | 160381239 | ||||||
chr3:160381239
|
A | AATATATA others(39): Show |
1 | a0002c0002t0002g0156 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.259+263_259+264ins others(46): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 3/19 | chr3 | 160381239 | ||||||
chr3:160381239
|
A | ATATATAT others(10): Show |
1 | a0002c0003t0002g0053 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.259+263_259+264ins others(17): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 3/19 | chr3 | 160381239 | ||||||
chr3:160381239
|
A | ATATATAT others(24): Show |
1 | a0002c0002t0002g0202 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.259+263_259+264ins others(31): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 3/19 | chr3 | 160381239 | ||||||
chr3:160381252
|
A | T | 3 | a0002c0002t0001g0047a0002c0002t0001g0066a0002c0002t0001g0067 | 3 | HG03710.hp1 HG04184.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.259+251T>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 3/19 | chr3 | 160381252 | ||||||
chr3:160381253
|
T | TA | 3 | a0002c0002t0001g0047a0002c0002t0001g0066a0002c0002t0001g0067 | 3 | HG03710.hp1 HG04184.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.259+249dupT | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 3/19 | chr3 | 160381253 | ||||||
chr3:160381266
|
T | A | 6 | a0002c0002t0001g0056a0002c0002t0001g0068a0002c0002t0001g0069others(3): Show | 6 | HG00735.hp1 HG00741.hp2 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.259+237A>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 3/19 | chr3 | 160381266 | ||||||
chr3:160381364
|
T | C | 1 | a0002c0002t0002g0055 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.259+139A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 3/19 | chr3 | 160381364 | ||||||
chr3:160381388
|
G | T | 1 | a0001c0001t0005g0093 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.259+115C>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 3/19 | chr3 | 160381388 | ||||||
chr3:160381398
|
T | C | 1 | a0002c0002t0002g0015 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.259+105A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 3/19 | chr3 | 160381398 | ||||||
chr3:160381402
|
G | A | 1 | a0001c0008t0001g0164 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.259+101C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 3/19 | chr3 | 160381402 | ||||||
chr3:160381773
|
A | G | 1 | a0002c0002t0002g0172 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.38-49T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 2/19 | chr3 | 160381773 | ||||||
chr3:160381867
|
A | AT | 43 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(40): Show | 46 | HG00099.hp2 HG01069.hp2 HG01243.hp1 others(43): Show |
intron_variant | MODIFIER | c.38-144dupA | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 2/19 | chr3 | 160381867 | ||||||
chr3:160381967
|
C | T | 1 | a0001c0001t0001g0189 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.38-243G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 2/19 | chr3 | 160381967 | ||||||
chr3:160381973
|
A | T | 6 | a0002c0002t0004g0018a0002c0002t0004g0019a0002c0002t0004g0020others(3): Show | 6 | HG02976.hp2 NA18960.hp1 NA18983.hp2 others(3): Show |
intron_variant | MODIFIER | c.38-249T>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 2/19 | chr3 | 160381973 | ||||||
chr3:160382899
|
C | A | 1 | a0002c0002t0003g0041 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.38-1175G>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 2/19 | chr3 | 160382899 | ||||||
chr3:160383161
|
A | G | 7 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(4): Show | 7 | HG00099.hp2 HG02976.hp1 HG03834.hp1 others(4): Show |
intron_variant | MODIFIER | c.37+1403T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 2/19 | chr3 | 160383161 | ||||||
chr3:160383538
|
G | A | 2 | a0001c0001t0001g0165a0001c0001t0001g0166 | 2 | HG03471.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.37+1026C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 2/19 | chr3 | 160383538 | ||||||
chr3:160383601
|
A | C | 7 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(4): Show | 7 | HG00099.hp2 HG02976.hp1 HG03834.hp1 others(4): Show |
intron_variant | MODIFIER | c.37+963T>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 2/19 | chr3 | 160383601 | ||||||
chr3:160383857
|
T | G | 2 | a0001c0001t0001g0148a0001c0001t0001g0149 | 2 | HG01106.hp1 HG01168.hp2 |
intron_variant | MODIFIER | c.37+707A>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 2/19 | chr3 | 160383857 | ||||||
chr3:160384018
|
G | C | 1 | a0002c0002t0002g0037 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.37+546C>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 2/19 | chr3 | 160384018 | ||||||
chr3:160384218
|
C | G | 15 | a0002c0002t0001g0033a0002c0002t0002g0003a0002c0002t0002g0032others(12): Show | 17 | HG01243.hp1 HG02451.hp2 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.37+346G>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 2/19 | chr3 | 160384218 | ||||||
chr3:160384245
|
C | CA | 88 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(85): Show | 89 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(86): Show |
intron_variant | MODIFIER | c.37+318dupT | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 2/19 | chr3 | 160384245 | ||||||
chr3:160384245
|
CA | C | 9 | a0002c0002t0002g0021a0002c0002t0002g0022a0002c0002t0002g0023others(6): Show | 9 | HG01255.hp2 HG02055.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.37+318delT | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 2/19 | chr3 | 160384245 | ||||||
chr3:160384346
|
G | A | 5 | a0002c0002t0002g0156a0002c0002t0002g0157a0002c0002t0002g0158others(2): Show | 5 | HG01167.hp2 HG01169.hp1 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.37+218C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 2/19 | chr3 | 160384346 | ||||||
chr3:160384373
|
A | G | 1 | a0002c0002t0007g0088 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.37+191T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 2/19 | chr3 | 160384373 | ||||||
chr3:160384381
|
C | T | 6 | a0002c0003t0002g0050a0002c0003t0002g0051a0002c0003t0002g0052others(3): Show | 6 | HG01891.hp2 HG02630.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.37+183G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 2/19 | chr3 | 160384381 | ||||||
chr3:160384699
|
C | T | 1 | a0001c0001t0001g0153 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-46-53G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160384699 | ||||||
chr3:160384703
|
T | C | 5 | a0002c0002t0002g0004a0002c0002t0002g0028a0002c0002t0002g0048others(2): Show | 6 | HG01069.hp2 HG02717.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.-46-57A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160384703 | ||||||
chr3:160384859
|
A | T | 8 | a0001c0001t0001g0017a0001c0001t0001g0094a0001c0001t0001g0095others(5): Show | 8 | HG02109.hp2 HG02258.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.-46-213T>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160384859 | ||||||
chr3:160385012
|
C | A | 13 | a0001c0001t0001g0006a0001c0001t0001g0171a0001c0001t0001g0189others(10): Show | 14 | HG00423.hp1 HG01433.hp2 HG01952.hp1 others(11): Show |
intron_variant | MODIFIER | c.-46-366G>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160385012 | ||||||
chr3:160385023
|
T | C | 1 | a0002c0002t0004g0020 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.-46-377A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160385023 | ||||||
chr3:160385138
|
C | T | 2 | a0001c0001t0001g0092a0001c0001t0001g0151 | 2 | HG01109.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.-46-492G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160385138 | ||||||
chr3:160385149
|
G | A | 2 | a0002c0002t0002g0004a0002c0002t0002g0028 | 3 | HG02886.hp2 HG03225.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-46-503C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160385149 | ||||||
chr3:160385187
|
G | A | 1 | a0002c0002t0001g0072 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-46-541C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160385187 | ||||||
chr3:160385282
|
A | G | 8 | a0001c0001t0001g0005a0001c0001t0001g0161a0001c0001t0001g0162others(5): Show | 9 | HG01433.hp1 HG02257.hp2 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.-46-636T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160385282 | ||||||
chr3:160385335
|
G | C | 28 | a0002c0002t0001g0046a0002c0002t0001g0047a0002c0002t0001g0056others(25): Show | 28 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(25): Show |
intron_variant | MODIFIER | c.-46-689C>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160385335 | ||||||
chr3:160385376
|
A | G | 1 | a0002c0006t0002g0014 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-46-730T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160385376 | ||||||
chr3:160385431
|
G | C | 5 | a0002c0002t0002g0156a0002c0002t0002g0157a0002c0002t0002g0158others(2): Show | 5 | HG01167.hp2 HG01169.hp1 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.-46-785C>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160385431 | ||||||
chr3:160385831
|
T | C | 1 | a0002c0002t0002g0015 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-46-1185A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160385831 | ||||||
chr3:160386236
|
T | C | 7 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(4): Show | 7 | HG00099.hp2 HG02976.hp1 HG03834.hp1 others(4): Show |
intron_variant | MODIFIER | c.-46-1590A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160386236 | ||||||
chr3:160386569
|
T | C | 1 | a0001c0001t0001g0090 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-46-1923A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160386569 | ||||||
chr3:160386583
|
G | T | 1 | a0002c0002t0002g0055 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-46-1937C>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160386583 | ||||||
chr3:160386711
|
C | T | 2 | a0001c0001t0001g0010a0001c0001t0001g0011 | 2 | NA18944.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.-46-2065G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160386711 | ||||||
chr3:160386975
|
T | C | 1 | a0002c0002t0002g0055 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-46-2329A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160386975 | ||||||
chr3:160387281
|
G | T | 1 | a0002c0002t0002g0055 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-46-2635C>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160387281 | ||||||
chr3:160387453
|
G | C | 28 | a0002c0002t0001g0046a0002c0002t0001g0047a0002c0002t0001g0056others(25): Show | 28 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(25): Show |
intron_variant | MODIFIER | c.-46-2807C>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160387453 | ||||||
chr3:160387461
|
G | A | 2 | a0003c0004t0002g0026a0003c0004t0002g0027 | 2 | HG01255.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.-46-2815C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160387461 | ||||||
chr3:160387970
|
T | C | 15 | a0002c0002t0001g0033a0002c0002t0002g0003a0002c0002t0002g0032others(12): Show | 17 | HG01243.hp1 HG02451.hp2 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.-46-3324A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160387970 | ||||||
chr3:160388021
|
G | T | 1 | a0002c0002t0002g0015 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-46-3375C>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160388021 | ||||||
chr3:160388036
|
AG | A | 7 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(4): Show | 7 | HG00099.hp2 HG02976.hp1 HG03834.hp1 others(4): Show |
intron_variant | MODIFIER | c.-46-3391delC | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160388036 | ||||||
chr3:160388216
|
CT | C | 8 | a0001c0001t0001g0147a0002c0002t0002g0004a0002c0002t0002g0028others(5): Show | 9 | HG00323.hp1 HG01891.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.-46-3571delA | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160388216 | ||||||
chr3:160388342
|
C | T | 39 | a0001c0001t0001g0006a0001c0001t0001g0168a0001c0001t0001g0169others(36): Show | 40 | HG00323.hp2 HG00423.hp1 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.-46-3696G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160388342 | ||||||
chr3:160388493
|
C | T | 5 | a0002c0002t0002g0156a0002c0002t0002g0157a0002c0002t0002g0158others(2): Show | 5 | HG01167.hp2 HG01169.hp1 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.-46-3847G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160388493 | ||||||
chr3:160388541
|
C | T | 1 | a0001c0001t0001g0017 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-46-3895G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160388541 | ||||||
chr3:160388551
|
T | C | 1 | a0002c0002t0002g0015 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-46-3905A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160388551 | ||||||
chr3:160388565
|
A | T | 5 | a0002c0002t0002g0004a0002c0002t0002g0028a0002c0002t0002g0048others(2): Show | 6 | HG01069.hp2 HG02717.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.-46-3919T>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160388565 | ||||||
chr3:160388654
|
T | G | 5 | a0002c0002t0002g0201a0002c0002t0002g0202a0002c0002t0002g0203others(2): Show | 5 | HG02258.hp2 HG02965.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.-46-4008A>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160388654 | ||||||
chr3:160388764
|
C | T | 1 | a0002c0002t0003g0002 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-46-4118G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160388764 | ||||||
chr3:160388903
|
G | A | 5 | a0002c0002t0002g0156a0002c0002t0002g0157a0002c0002t0002g0158others(2): Show | 5 | HG01167.hp2 HG01169.hp1 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.-46-4257C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160388903 | ||||||
chr3:160388993
|
C | T | 127 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(124): Show | 131 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(128): Show |
intron_variant | MODIFIER | c.-46-4347G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160388993 | ||||||
chr3:160389042
|
A | C | 1 | a0002c0002t0002g0083 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-46-4396T>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160389042 | ||||||
chr3:160389312
|
C | T | 28 | a0002c0002t0001g0046a0002c0002t0001g0047a0002c0002t0001g0056others(25): Show | 28 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(25): Show |
intron_variant | MODIFIER | c.-46-4666G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160389312 | ||||||
chr3:160389424
|
C | T | 8 | a0001c0001t0001g0005a0001c0001t0001g0161a0001c0001t0001g0162others(5): Show | 9 | HG01433.hp1 HG02257.hp2 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.-46-4778G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160389424 | ||||||
chr3:160389502
|
C | A | 7 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(4): Show | 7 | HG00099.hp2 HG02976.hp1 HG03834.hp1 others(4): Show |
intron_variant | MODIFIER | c.-46-4856G>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160389502 | ||||||
chr3:160389665
|
A | G | 1 | a0001c0001t0001g0091 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.-46-5019T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160389665 | ||||||
chr3:160389691
|
C | T | 7 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(4): Show | 7 | HG00099.hp2 HG02976.hp1 HG03834.hp1 others(4): Show |
intron_variant | MODIFIER | c.-46-5045G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160389691 | ||||||
chr3:160389704
|
C | T | 1 | a0001c0001t0001g0154 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-46-5058G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160389704 | ||||||
chr3:160390020
|
G | A | 1 | a0002c0006t0002g0014 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-46-5374C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160390020 | ||||||
chr3:160390050
|
T | C | 1 | a0002c0002t0002g0083 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-46-5404A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160390050 | ||||||
chr3:160390193
|
G | A | 1 | a0002c0002t0002g0083 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-46-5547C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160390193 | ||||||
chr3:160390272
|
C | T | 5 | a0002c0002t0002g0004a0002c0002t0002g0028a0002c0002t0002g0048others(2): Show | 6 | HG01069.hp2 HG02717.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.-46-5626G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160390272 | ||||||
chr3:160390372
|
G | A | 1 | a0004c0005t0009g0087 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-46-5726C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160390372 | ||||||
chr3:160390417
|
C | CAAAAAA | 15 | a0002c0002t0001g0033a0002c0002t0002g0003a0002c0002t0002g0032others(12): Show | 17 | HG01243.hp1 HG02451.hp2 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.-46-5777_-46-5772d others(8): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160390417 | ||||||
chr3:160390536
|
T | C | 1 | a0002c0006t0002g0014 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-46-5890A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160390536 | ||||||
chr3:160390591
|
T | C | 3 | a0002c0002t0001g0076a0002c0002t0001g0077a0002c0002t0001g0078 | 3 | HG02622.hp1 HG02818.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-46-5945A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160390591 | ||||||
chr3:160390798
|
T | C | 5 | a0002c0002t0002g0004a0002c0002t0002g0028a0002c0002t0002g0048others(2): Show | 6 | HG01069.hp2 HG02717.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.-46-6152A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160390798 | ||||||
chr3:160391055
|
G | A | 1 | a0002c0002t0002g0083 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-46-6409C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160391055 | ||||||
chr3:160391252
|
C | T | 1 | a0001c0001t0001g0090 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-46-6606G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160391252 | ||||||
chr3:160391300
|
A | G | 2 | a0002c0002t0003g0030a0002c0002t0003g0031 | 2 | HG02451.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.-46-6654T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160391300 | ||||||
chr3:160391561
|
C | T | 5 | a0002c0002t0002g0156a0002c0002t0002g0157a0002c0002t0002g0158others(2): Show | 5 | HG01167.hp2 HG01169.hp1 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.-46-6915G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160391561 | ||||||
chr3:160391600
|
G | A | 1 | a0001c0001t0006g0198 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.-46-6954C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160391600 | ||||||
chr3:160391688
|
A | G | 1 | a0001c0001t0001g0089 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-46-7042T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160391688 | ||||||
chr3:160391809
|
T | A | 1 | a0002c0002t0002g0015 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-46-7163A>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160391809 | ||||||
chr3:160391860
|
C | T | 43 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(40): Show | 46 | HG00099.hp2 HG01069.hp2 HG01243.hp1 others(43): Show |
intron_variant | MODIFIER | c.-46-7214G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160391860 | ||||||
chr3:160391869
|
A | G | 126 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(123): Show | 130 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(127): Show |
intron_variant | MODIFIER | c.-46-7223T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160391869 | ||||||
chr3:160391944
|
C | T | 1 | a0002c0002t0007g0088 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-47+7202G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160391944 | ||||||
chr3:160391969
|
G | T | 1 | a0001c0001t0001g0175 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-47+7177C>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160391969 | ||||||
chr3:160392424
|
G | A | 9 | a0002c0003t0002g0050a0002c0003t0002g0051a0002c0003t0002g0052others(6): Show | 9 | HG00738.hp2 HG01167.hp1 HG01261.hp1 others(6): Show |
intron_variant | MODIFIER | c.-47+6722C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160392424 | ||||||
chr3:160392467
|
G | A | 34 | a0001c0001t0001g0006a0001c0001t0001g0168a0001c0001t0001g0169others(31): Show | 35 | HG00323.hp2 HG00423.hp1 HG00642.hp2 others(32): Show |
intron_variant | MODIFIER | c.-47+6679C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160392467 | ||||||
chr3:160392745
|
T | C | 2 | a0001c0001t0001g0148a0001c0001t0001g0149 | 2 | HG01106.hp1 HG01168.hp2 |
intron_variant | MODIFIER | c.-47+6401A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160392745 | ||||||
chr3:160392894
|
A | AC | 19 | a0002c0002t0002g0004a0002c0002t0002g0021a0002c0002t0002g0022others(16): Show | 20 | HG01069.hp2 HG02055.hp1 HG02280.hp2 others(17): Show |
intron_variant | MODIFIER | c.-47+6251dupG | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160392894 | ||||||
chr3:160393133
|
C | A | 5 | a0002c0002t0002g0156a0002c0002t0002g0157a0002c0002t0002g0158others(2): Show | 5 | HG01167.hp2 HG01169.hp1 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.-47+6013G>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160393133 | ||||||
chr3:160393348
|
G | A | 1 | a0002c0006t0002g0014 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-47+5798C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160393348 | ||||||
chr3:160393623
|
G | A | 3 | a0002c0002t0001g0073a0002c0002t0001g0074a0002c0002t0001g0075 | 3 | HG00140.hp1 HG01106.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.-47+5523C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160393623 | ||||||
chr3:160393656
|
T | C | 8 | a0002c0002t0002g0021a0002c0002t0002g0022a0002c0002t0002g0023others(5): Show | 8 | HG01255.hp2 HG02055.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.-47+5490A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160393656 | ||||||
chr3:160393671
|
T | C | 1 | a0001c0001t0001g0150 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.-47+5475A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160393671 | ||||||
chr3:160394069
|
T | G | 5 | a0002c0003t0002g0050a0002c0003t0002g0051a0002c0003t0002g0052others(2): Show | 5 | HG01891.hp2 HG02630.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-47+5077A>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160394069 | ||||||
chr3:160394101
|
C | T | 21 | a0002c0002t0002g0004a0002c0002t0002g0021a0002c0002t0002g0022others(18): Show | 22 | HG01069.hp2 HG01255.hp2 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.-47+5045G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160394101 | ||||||
chr3:160394104
|
T | C | 2 | a0002c0002t0002g0004a0002c0002t0002g0028 | 3 | HG02886.hp2 HG03225.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-47+5042A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160394104 | ||||||
chr3:160394172
|
A | T | 25 | a0002c0002t0001g0046a0002c0002t0001g0047a0002c0002t0001g0056others(22): Show | 25 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(22): Show |
intron_variant | MODIFIER | c.-47+4974T>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160394172 | ||||||
chr3:160394278
|
T | A | 3 | a0002c0002t0002g0048a0002c0002t0002g0049a0002c0002t0002g0082 | 3 | HG01069.hp2 HG02717.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.-47+4868A>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160394278 | ||||||
chr3:160394546
|
T | A | 5 | a0002c0003t0002g0050a0002c0003t0002g0051a0002c0003t0002g0052others(2): Show | 5 | HG01891.hp2 HG02630.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-47+4600A>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160394546 | ||||||
chr3:160394642
|
G | A | 1 | a0001c0001t0001g0151 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-47+4504C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160394642 | ||||||
chr3:160394756
|
GA | G | 26 | a0002c0002t0001g0046a0002c0002t0001g0047a0002c0002t0001g0056others(23): Show | 26 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(23): Show |
intron_variant | MODIFIER | c.-47+4389delT | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160394756 | ||||||
chr3:160395036
|
T | C | 1 | a0002c0002t0002g0015 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-47+4110A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160395036 | ||||||
chr3:160395329
|
T | C | 1 | a0002c0002t0002g0015 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-47+3817A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160395329 | ||||||
chr3:160395429
|
T | C | 15 | a0002c0002t0001g0033a0002c0002t0002g0003a0002c0002t0002g0032others(12): Show | 17 | HG01243.hp1 HG02451.hp2 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.-47+3717A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160395429 | ||||||
chr3:160395672
|
G | T | 1 | a0001c0001t0001g0174 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-47+3474C>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160395672 | ||||||
chr3:160395681
|
A | T | 126 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(123): Show | 130 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(127): Show |
intron_variant | MODIFIER | c.-47+3465T>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160395681 | ||||||
chr3:160395966
|
G | A | 1 | a0001c0001t0001g0152 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.-47+3180C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160395966 | ||||||
chr3:160396032
|
G | A | 1 | a0002c0002t0002g0015 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-47+3114C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160396032 | ||||||
chr3:160396056
|
T | C | 1 | a0002c0002t0002g0055 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-47+3090A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160396056 | ||||||
chr3:160396223
|
T | G | 1 | a0001c0001t0001g0167 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-47+2923A>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160396223 | ||||||
chr3:160396345
|
T | A | 1 | a0002c0002t0003g0029 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-47+2801A>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160396345 | ||||||
chr3:160396346
|
C | A | 1 | a0002c0002t0003g0029 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-47+2800G>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160396346 | ||||||
chr3:160396346
|
CAT | C | 32 | a0001c0001t0001g0006a0001c0001t0001g0168a0001c0001t0001g0169others(29): Show | 33 | HG00323.hp2 HG00423.hp1 HG00642.hp2 others(30): Show |
intron_variant | MODIFIER | c.-47+2798_-47+2799d others(4): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160396346 | ||||||
chr3:160396347
|
A | G | 1 | a0002c0002t0003g0029 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-47+2799T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160396347 | ||||||
chr3:160396360
|
T | A | 1 | a0002c0002t0003g0029 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-47+2786A>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160396360 | ||||||
chr3:160396369
|
T | G | 1 | a0002c0002t0003g0029 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-47+2777A>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160396369 | ||||||
chr3:160396384
|
T | G | 1 | a0002c0002t0003g0029 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-47+2762A>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160396384 | ||||||
chr3:160396398
|
T | A | 1 | a0002c0002t0003g0029 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-47+2748A>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160396398 | ||||||
chr3:160396399
|
T | A | 1 | a0002c0002t0003g0029 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-47+2747A>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160396399 | ||||||
chr3:160396404
|
A | G | 1 | a0002c0002t0003g0029 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-47+2742T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160396404 | ||||||
chr3:160396409
|
T | A | 1 | a0002c0002t0003g0029 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-47+2737A>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160396409 | ||||||
chr3:160396410
|
T | G | 1 | a0002c0002t0003g0029 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-47+2736A>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160396410 | ||||||
chr3:160396413
|
T | A | 1 | a0002c0002t0003g0029 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-47+2733A>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160396413 | ||||||
chr3:160396419
|
A | G | 1 | a0002c0002t0003g0029 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-47+2727T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160396419 | ||||||
chr3:160396422
|
T | G | 1 | a0002c0002t0003g0029 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-47+2724A>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160396422 | ||||||
chr3:160396430
|
G | T | 1 | a0002c0002t0003g0029 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-47+2716C>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160396430 | ||||||
chr3:160396435
|
T | C | 1 | a0002c0002t0003g0029 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-47+2711A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160396435 | ||||||
chr3:160396436
|
C | T | 1 | a0002c0002t0003g0029 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-47+2710G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160396436 | ||||||
chr3:160396458
|
G | T | 1 | a0002c0002t0003g0029 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-47+2688C>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160396458 | ||||||
chr3:160396461
|
A | T | 1 | a0002c0002t0003g0029 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-47+2685T>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160396461 | ||||||
chr3:160396481
|
A | T | 1 | a0002c0002t0003g0029 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-47+2665T>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160396481 | ||||||
chr3:160396547
|
C | T | 1 | a0002c0002t0002g0015 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-47+2599G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160396547 | ||||||
chr3:160396775
|
T | C | 1 | a0002c0002t0002g0083 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-47+2371A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160396775 | ||||||
chr3:160397035
|
T | C | 7 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(4): Show | 7 | HG00099.hp2 HG02976.hp1 HG03834.hp1 others(4): Show |
intron_variant | MODIFIER | c.-47+2111A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160397035 | ||||||
chr3:160397177
|
CCA | C | 22 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(19): Show | 24 | HG00099.hp2 HG01243.hp1 HG02451.hp2 others(21): Show |
intron_variant | MODIFIER | c.-47+1967_-47+1968d others(4): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160397177 | ||||||
chr3:160397216
|
C | T | 126 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(123): Show | 130 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(127): Show |
intron_variant | MODIFIER | c.-47+1930G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160397216 | ||||||
chr3:160397586
|
T | C | 2 | a0002c0002t0001g0084a0002c0002t0001g0085 | 2 | HG02602.hp1 HG03490.hp2 |
intron_variant | MODIFIER | c.-47+1560A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160397586 | ||||||
chr3:160397716
|
C | CT | 59 | a0001c0001t0001g0006a0001c0001t0001g0174a0001c0001t0001g0175others(56): Show | 60 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(57): Show |
intron_variant | MODIFIER | c.-47+1429dupA | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160397716 | ||||||
chr3:160397716
|
C | CTT | 18 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(15): Show | 18 | HG00642.hp2 HG00738.hp1 HG01109.hp2 others(15): Show |
intron_variant | MODIFIER | c.-47+1428_-47+1429d others(4): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160397716 | ||||||
chr3:160397716
|
C | CTTT | 23 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(20): Show | 26 | HG00099.hp2 HG01243.hp1 HG02451.hp2 others(23): Show |
intron_variant | MODIFIER | c.-47+1427_-47+1429d others(5): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160397716 | ||||||
chr3:160397716
|
C | CTTTT | 11 | a0002c0002t0002g0021a0002c0002t0002g0022a0002c0002t0002g0023others(8): Show | 11 | HG01255.hp2 HG02055.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.-47+1426_-47+1429d others(6): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160397716 | ||||||
chr3:160397716
|
CTTTTT | C | 5 | a0002c0002t0002g0201a0002c0002t0002g0202a0002c0002t0002g0203others(2): Show | 5 | HG02258.hp2 HG02965.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.-47+1425_-47+1429d others(7): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160397716 | ||||||
chr3:160397724
|
T | C | 1 | a0001c0001t0001g0153 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-47+1422A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160397724 | ||||||
chr3:160397744
|
G | T | 5 | a0002c0002t0002g0156a0002c0002t0002g0157a0002c0002t0002g0158others(2): Show | 5 | HG01167.hp2 HG01169.hp1 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.-47+1402C>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160397744 | ||||||
chr3:160397821
|
A | C | 1 | a0001c0001t0001g0017 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-47+1325T>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160397821 | ||||||
chr3:160397980
|
C | T | 203 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(200): Show | 210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.-47+1166G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160397980 | ||||||
chr3:160398046
|
T | C | 9 | a0002c0002t0002g0156a0002c0002t0002g0157a0002c0002t0002g0158others(6): Show | 9 | HG01167.hp2 HG01169.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.-47+1100A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160398046 | ||||||
chr3:160398194
|
A | G | 1 | a0001c0001t0001g0016 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.-47+952T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160398194 | ||||||
chr3:160398381
|
C | A | 1 | a0002c0002t0002g0015 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-47+765G>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160398381 | ||||||
chr3:160398386
|
T | C | 8 | a0001c0001t0001g0005a0001c0001t0001g0161a0001c0001t0001g0162others(5): Show | 9 | HG01433.hp1 HG02257.hp2 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.-47+760A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160398386 | ||||||
chr3:160398414
|
G | T | 1 | a0002c0002t0002g0015 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-47+732C>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160398414 | ||||||
chr3:160398587
|
C | T | 1 | a0002c0006t0002g0014 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-47+559G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160398587 | ||||||
chr3:160398964
|
C | T | 7 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(4): Show | 7 | HG00099.hp2 HG02976.hp1 HG03834.hp1 others(4): Show |
intron_variant | MODIFIER | c.-47+182G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160398964 | ||||||
chr3:160399019
|
T | G | 39 | a0001c0001t0001g0006a0001c0001t0001g0168a0001c0001t0001g0169others(36): Show | 40 | HG00323.hp2 HG00423.hp1 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.-47+127A>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160399019 |