geneid | 112752 |
---|---|
ensemblid | ENSG00000119650.13 |
hgncid | 29669 |
symbol | IFT43 |
name | intraflagellar transport 43 |
refseq_nuc | NM_001102564.3 |
refseq_prot | NP_001096034.1 |
ensembl_nuc | ENST00000314067.11 |
ensembl_prot | ENSP00000324177.6 |
mane_status | MANE Select |
chr | chr14 |
start | 75985763 |
end | 76083742 |
strand | + |
ver | v1.2 |
region | chr14:75985763-76083742 |
region5000 | chr14:75980763-76088742 |
regionname0 | IFT43_chr14_75985763_76083742 |
regionname5000 | IFT43_chr14_75980763_76088742 |
ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 208 | 392 | 92 | 76 | 168 | 12 | 42 | 132 | IFT43_chr14_75980763_76088742 | IFT43 | copy fasta | chr14 | 75980763 | 76088742 |
a0002 | 0/0 | 208 | 4 | 0 | 0 | 4 | 0 | 0 | 2 | IFT43_chr14_75980763_76088742 | IFT43 | copy fasta | chr14 | 75980763 | 76088742 |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 627 | 388 | 92 | 76 | 165 | 12 | 41 | IFT43_chr14_75980763_76088742 | IFT43 | copy fasta | chr14 | 75980763 | 76088742 |
c0002 | 0/0 | 627 | 4 | 0 | 0 | 4 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | copy fasta | chr14 | 75980763 | 76088742 |
c0003 | 0/0 | 627 | 3 | 0 | 0 | 3 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | copy fasta | chr14 | 75980763 | 76088742 |
c0004 | 0/0 | 627 | 1 | 0 | 0 | 0 | 0 | 1 | IFT43_chr14_75980763_76088742 | IFT43 | copy fasta | chr14 | 75980763 | 76088742 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 190 | 396 | 92 | 76 | 172 | 12 | 42 | IFT43_chr14_75980763_76088742 | IFT43 | copy fasta | chr14 | 75980763 | 76088742 |
ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 5 | 1 | 4 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0012 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0109 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0211 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0221 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0240 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0241 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0243 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0244 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0270 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0289 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0322 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0336 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0337 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0340 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0347 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0349 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0351 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0364 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0365 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0366 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0367 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0368 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0369 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0370 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0371 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0372 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0373 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0374 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0375 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0376 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0377 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0378 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0379 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
g0380 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 627 | 388 | 92 | 76 | 165 | 12 | 41 | IFT43_chr14_75980763_76088742 | IFT43 | copy fasta | chr14 | 75980763 | 76088742 |
a0001c0003 | 0/0 | 627 | 3 | 0 | 0 | 3 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | copy fasta | chr14 | 75980763 | 76088742 |
a0001c0004 | 0/0 | 627 | 1 | 0 | 0 | 0 | 0 | 1 | IFT43_chr14_75980763_76088742 | IFT43 | copy fasta | chr14 | 75980763 | 76088742 |
a0002c0002 | 0/0 | 627 | 4 | 0 | 0 | 4 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | copy fasta | chr14 | 75980763 | 76088742 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 816 | 388 | 92 | 76 | 165 | 12 | 41 | IFT43_chr14_75980763_76088742 | IFT43 | copy fasta | chr14 | 75980763 | 76088742 |
a0001c0003t0001 | 0/0 | 816 | 3 | 0 | 0 | 3 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | copy fasta | chr14 | 75980763 | 76088742 |
a0001c0004t0001 | 0/0 | 816 | 1 | 0 | 0 | 0 | 0 | 1 | IFT43_chr14_75980763_76088742 | IFT43 | copy fasta | chr14 | 75980763 | 76088742 |
a0002c0002t0001 | 0/0 | 816 | 4 | 0 | 0 | 4 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | copy fasta | chr14 | 75980763 | 76088742 |
actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 5 | 1 | 4 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0322 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0336 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0337 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0340 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0347 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0349 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0351 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0364 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0365 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0366 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0367 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0368 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0369 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0370 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0371 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0372 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0373 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0374 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0375 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0376 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0377 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0378 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0379 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0380 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0003t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0003t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0003t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0004t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0002c0002t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0002c0002t0001g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0002c0002t0001g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0002c0002t0001g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0071 | EUR | GBR | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0221 | EUR | GBR | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0179 | EUR | FIN | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0240 | EUR | FIN | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0342 | EAS | CHS | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0264 | EAS | CHS | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG00423 | hp1 | a0001 | c0003 | t0001 | g0008 | EAS | CHS | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | CHS | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | CHS | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0297 | EAS | CHS | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | CHS | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | CHS | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG00609 | hp1 | a0001 | c0003 | t0001 | g0200 | EAS | CHS | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | CHS | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0365 | AMR | PUR | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0285 | AMR | PUR | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0260 | EAS | CHS | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0343 | EAS | CHS | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0072 | AMR | PUR | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0242 | AMR | PUR | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0321 | AMR | PUR | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0174 | AMR | PUR | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0143 | AMR | PUR | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0085 | AMR | PUR | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0126 | AMR | PUR | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0237 | AMR | PUR | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0236 | AMR | PUR | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0054 | AMR | PUR | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0029 | AMR | PUR | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0138 | AMR | PUR | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0189 | AMR | PUR | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0089 | AMR | PUR | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0245 | AMR | PUR | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0167 | AMR | PUR | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0369 | AMR | PUR | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0227 | AMR | PUR | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0269 | AMR | PUR | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0222 | AMR | PUR | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0084 | AMR | PUR | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0046 | AMR | PUR | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0073 | AMR | PUR | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0171 | AMR | PUR | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0238 | AMR | PUR | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0059 | AMR | PUR | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0053 | AMR | PUR | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0366 | AMR | CLM | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0180 | AMR | CLM | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0229 | AMR | CLM | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0228 | AMR | CLM | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0070 | AMR | CLM | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0181 | AMR | CLM | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0271 | AMR | CLM | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0218 | AMR | CLM | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0210 | AMR | CLM | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0268 | AMR | CLM | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0107 | AMR | CLM | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0106 | AMR | CLM | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0182 | AMR | CLM | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0293 | AMR | CLM | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0175 | AMR | CLM | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0211 | EUR | IBS | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0109 | EUR | IBS | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0270 | EUR | IBS | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0289 | EUR | IBS | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0288 | AFR | ACB | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | ACB | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0265 | AFR | ACB | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0159 | AMR | PEL | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0044 | AMR | PEL | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0239 | AMR | PEL | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0045 | AMR | PEL | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0153 | AMR | PEL | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0294 | AMR | PEL | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0047 | AMR | PEL | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0364 | AMR | PEL | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0323 | AMR | PEL | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0151 | AMR | PEL | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0160 | AMR | PEL | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0049 | AMR | PEL | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0217 | AMR | PEL | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PEL | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | KHV | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | KHV | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | KHV | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0358 | EAS | KHV | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | KHV | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0375 | EAS | KHV | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0380 | AFR | ACB | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0235 | AFR | ACB | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | KHV | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG02056 | hp2 | a0002 | c0002 | t0001 | g0362 | EAS | KHV | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0295 | EAS | KHV | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | KHV | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | KHV | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0304 | EAS | KHV | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0317 | EAS | KHV | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | KHV | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0374 | EAS | KHV | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | KHV | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0161 | AMR | PEL | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0320 | AMR | PEL | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG02155 | hp1 | a0001 | c0003 | t0001 | g0183 | EAS | CDX | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG02155 | hp2 | a0002 | c0002 | t0001 | g0319 | EAS | CDX | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | CDX | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0330 | EAS | CDX | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0078 | AFR | ACB | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0344 | AFR | ACB | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0246 | AFR | ACB | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0284 | AFR | ACB | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0267 | AMR | PEL | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0152 | AMR | PEL | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0150 | AFR | ACB | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0114 | AFR | ACB | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0148 | AMR | PEL | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0048 | AMR | PEL | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0081 | AFR | ACB | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0116 | AFR | ACB | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | KHV | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0095 | AFR | GWD | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0077 | AFR | GWD | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0351 | SAS | PJL | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0104 | SAS | PJL | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0135 | AFR | GWD | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0255 | AFR | GWD | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0065 | AFR | GWD | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | GWD | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0082 | AFR | GWD | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0247 | AFR | GWD | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0133 | SAS | PJL | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0209 | SAS | PJL | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0177 | SAS | PJL | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0216 | SAS | PJL | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0079 | AFR | GWD | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0291 | AFR | GWD | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0118 | AFR | GWD | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0324 | SAS | PJL | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0286 | SAS | PJL | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0215 | SAS | PJL | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0113 | SAS | PJL | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | GWD | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0299 | AFR | GWD | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0080 | AFR | GWD | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0036 | AFR | GWD | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0115 | AFR | GWD | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | GWD | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0254 | AFR | GWD | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | GWD | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0253 | AFR | GWD | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0051 | AFR | GWD | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0087 | AFR | ESN | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0094 | AFR | ESN | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0058 | AFR | ESN | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | ESN | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0050 | AFR | ESN | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0074 | AFR | ESN | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0061 | AFR | ESN | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | ESN | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0315 | SAS | PJL | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0303 | SAS | PJL | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0075 | AFR | GWD | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | GWD | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0250 | AFR | MSL | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0057 | AFR | MSL | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0251 | AFR | ESN | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0099 | AFR | ESN | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0372 | AFR | ESN | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0248 | AFR | ESN | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0069 | AFR | ESN | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0062 | AFR | MSL | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0290 | AFR | MSL | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0108 | SAS | PJL | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0111 | SAS | PJL | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0083 | AFR | MSL | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | MSL | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0142 | SAS | PJL | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0012 | SAS | PJL | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0147 | SAS | PJL | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0012 | SAS | PJL | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0371 | AFR | ESN | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | ESN | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0298 | AFR | GWD | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0287 | AFR | GWD | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | MSL | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0105 | AFR | MSL | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0149 | SAS | PJL | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0232 | SAS | PJL | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0336 | SAS | PJL | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0234 | SAS | PJL | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0373 | SAS | STU | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0230 | SAS | STU | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0088 | SAS | PJL | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0144 | SAS | PJL | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0178 | SAS | PJL | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG03710 | hp2 | a0001 | c0004 | t0001 | g0231 | SAS | PJL | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0141 | SAS | BEB | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0347 | SAS | BEB | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0120 | SAS | BEB | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0306 | SAS | BEB | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0119 | SAS | BEB | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0056 | SAS | BEB | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0349 | SAS | BEB | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0165 | SAS | BEB | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0145 | SAS | STU | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0314 | SAS | STU | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0226 | SAS | BEB | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0326 | SAS | BEB | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0281 | AFR | YRI | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0283 | AFR | YRI | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0335 | EAS | CHB | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0301 | EAS | CHB | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | CHB | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0312 | EAS | CHB | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0100 | AFR | YRI | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0052 | AFR | YRI | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0361 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0355 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0338 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0331 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0377 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0353 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0346 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0378 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0316 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0313 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0309 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA18972 | hp1 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0327 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0352 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0354 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0318 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0308 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0350 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA18987 | hp1 | a0001 | c0001 | t0001 | g0305 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA18987 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0310 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA18995 | hp1 | a0002 | c0002 | t0001 | g0357 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA18997 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA18997 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0333 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0363 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0376 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0092 | AFR | LWK | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0060 | AFR | LWK | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0256 | AFR | LWK | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0066 | AFR | LWK | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0367 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA19055 | hp1 | a0001 | c0001 | t0001 | g0311 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA19055 | hp2 | a0001 | c0001 | t0001 | g0341 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0300 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0328 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0360 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0302 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0307 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0329 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA19075 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA19075 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0379 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0348 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0332 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0334 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0345 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA19090 | hp1 | a0002 | c0002 | t0001 | g0356 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0359 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0076 | AFR | YRI | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0132 | AFR | YRI | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0090 | AFR | ASW | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0176 | AFR | ASW | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0127 | EUR | TSI | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0244 | EUR | TSI | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0241 | EUR | TSI | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0243 | EUR | TSI | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0337 | SAS | GIH | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0043 | SAS | GIH | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0339 | AMR | CLM | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0325 | AMR | CLM | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0292 | AFR | ACB | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0093 | AFR | ACB | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0117 | AFR | ACB | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0368 | AFR | ACB | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | ACB | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0249 | AFR | ACB | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0370 | AFR | MSL | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0096 | AFR | MSL | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0252 | AFR | USA | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | USA | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | USA | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | USA | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | LWK | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0098 | AFR | LWK | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0322 | REF | REF | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0340 | REF | REF | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:76059332
|
G | A | 1 | a0002 | 4 | HG02056.hp2 HG02155.hp2 NA18995.hp1 others(1): Show |
missense_variant | MODERATE | c.254G>A | p.Arg85His | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/9 | 278/816 | 254/627 | 85/208 | chr14 | 76059332 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:76083250
|
C | T | 1 | a0001c0004 | 1 | HG03710.hp2 | synonymous_variant | LOW | c.468C>T | p.Leu156Leu | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 8/9 | 492/816 | 468/627 | 156/208 | chr14 | 76083250 | ||
chr14:76083268
|
G | A | 1 | a0001c0003 | 3 | HG00423.hp1 HG00609.hp1 HG02155.hp1 |
synonymous_variant | LOW | c.486G>A | p.Ala162Ala | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 8/9 | 510/816 | 486/627 | 162/208 | chr14 | 76083268 |
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 |
---|
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:75985968
|
A | G | 1 | a0001c0001t0001g0380 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.54+128A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 1/8 | chr14 | 75985968 | ||||||
chr14:75986137
|
C | T | 6 | a0001c0001t0001g0374a0001c0001t0001g0375a0001c0001t0001g0376others(3): Show | 6 | HG02040.hp2 HG02135.hp1 NA18950.hp1 others(3): Show |
intron_variant | MODIFIER | c.54+297C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 1/8 | chr14 | 75986137 | ||||||
chr14:75986166
|
G | A | 4 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(1): Show | 4 | HG02630.hp1 HG02723.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.54+326G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 1/8 | chr14 | 75986166 | ||||||
chr14:75986172
|
A | G | 6 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(3): Show | 7 | HG02630.hp1 HG02723.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.54+332A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 1/8 | chr14 | 75986172 | ||||||
chr14:75986184
|
G | A | 1 | a0001c0001t0001g0374 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.54+344G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 1/8 | chr14 | 75986184 | ||||||
chr14:75986269
|
T | A | 2 | a0001c0001t0001g0017a0001c0001t0001g0018 | 2 | HG00597.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.54+429T>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 1/8 | chr14 | 75986269 | ||||||
chr14:75986410
|
T | G | 1 | a0001c0001t0001g0019 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.54+570T>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 1/8 | chr14 | 75986410 | ||||||
chr14:75986446
|
C | CA | 214 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(211): Show | 219 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(216): Show |
intron_variant | MODIFIER | c.54+622dupA | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr14 | 75986446 | |||||
chr14:75986446
|
C | CAA | 42 | a0001c0001t0001g0003a0001c0001t0001g0020a0001c0001t0001g0021others(39): Show | 43 | HG01074.hp1 HG01081.hp1 HG01175.hp1 others(40): Show |
intron_variant | MODIFIER | c.54+621_54+622dupAA | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr14 | 75986446 | |||||
chr14:75986537
|
A | G | 8 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(5): Show | 8 | HG01109.hp2 HG02486.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.54+697A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 1/8 | chr14 | 75986537 | ||||||
chr14:75986540
|
C | G | 10 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0015others(7): Show | 11 | HG01109.hp2 HG02486.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.54+700C>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 1/8 | chr14 | 75986540 | ||||||
chr14:75986542
|
A | G | 1 | a0001c0001t0001g0265 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.54+702A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 1/8 | chr14 | 75986542 | ||||||
chr14:75986548
|
C | T | 8 | a0001c0001t0001g0257a0001c0001t0001g0258a0001c0001t0001g0259others(5): Show | 8 | HG00408.hp2 HG00673.hp1 NA18941.hp2 others(5): Show |
intron_variant | MODIFIER | c.54+708C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 1/8 | chr14 | 75986548 | ||||||
chr14:75986549
|
A | G | 1 | a0001c0001t0001g0016 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.54+709A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 1/8 | chr14 | 75986549 | ||||||
chr14:75986567
|
A | C | 1 | a0001c0001t0001g0367 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.54+727A>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 1/8 | chr14 | 75986567 | ||||||
chr14:75986629
|
C | T | 2 | a0001c0001t0001g0012a0001c0001t0001g0373 | 3 | HG03491.hp2 HG03492.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.54+789C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 1/8 | chr14 | 75986629 | ||||||
chr14:75986753
|
G | T | 2 | a0001c0001t0001g0012a0001c0001t0001g0373 | 3 | HG03491.hp2 HG03492.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.54+913G>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 1/8 | chr14 | 75986753 | ||||||
chr14:75986754
|
C | A | 2 | a0001c0001t0001g0012a0001c0001t0001g0373 | 3 | HG03491.hp2 HG03492.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.54+914C>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 1/8 | chr14 | 75986754 | ||||||
chr14:75986809
|
C | G | 1 | a0001c0001t0001g0256 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.54+969C>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 1/8 | chr14 | 75986809 | ||||||
chr14:75986841
|
T | TA | 8 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(5): Show | 8 | HG01109.hp2 HG02486.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.54+1002dupA | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr14 | 75986841 | |||||
chr14:75986844
|
G | A | 1 | a0001c0001t0001g0061 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.54+1004G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 1/8 | chr14 | 75986844 | ||||||
chr14:75986939
|
G | T | 6 | a0001c0001t0001g0009a0001c0001t0001g0251a0001c0001t0001g0252others(3): Show | 7 | HG01891.hp2 HG02615.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.54+1099G>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 1/8 | chr14 | 75986939 | ||||||
chr14:75987038
|
A | T | 2 | a0001c0001t0001g0249a0001c0001t0001g0250 | 2 | HG02559.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.54+1198A>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 1/8 | chr14 | 75987038 | ||||||
chr14:75987071
|
C | T | 1 | a0001c0001t0001g0256 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.54+1231C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 1/8 | chr14 | 75987071 | ||||||
chr14:75987110
|
C | G | 1 | a0001c0001t0001g0366 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.54+1270C>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 1/8 | chr14 | 75987110 | ||||||
chr14:75987252
|
A | G | 2 | a0001c0001t0001g0013a0001c0001t0001g0380 | 2 | HG02055.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.54+1412A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 1/8 | chr14 | 75987252 | ||||||
chr14:75987460
|
G | A | 1 | a0001c0001t0001g0062 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.55-1425G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 1/8 | chr14 | 75987460 | ||||||
chr14:75987555
|
A | G | 4 | a0001c0001t0001g0246a0001c0001t0001g0247a0001c0001t0001g0248others(1): Show | 4 | HG02258.hp1 HG02647.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.55-1330A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 1/8 | chr14 | 75987555 | ||||||
chr14:75987776
|
C | T | 119 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(116): Show | 122 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(119): Show |
intron_variant | MODIFIER | c.55-1109C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 1/8 | chr14 | 75987776 | ||||||
chr14:75987815
|
AATTTTGA others(3): Show |
A | 1 | a0001c0001t0001g0133 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.55-1069_55-1060del others(10): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 1/8 | chr14 | 75987815 | ||||||
chr14:75988085
|
C | A | 7 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0368others(4): Show | 7 | HG01109.hp2 HG02486.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.55-800C>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 1/8 | chr14 | 75988085 | ||||||
chr14:75988176
|
T | C | 1 | a0001c0001t0001g0020 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.55-709T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 1/8 | chr14 | 75988176 | ||||||
chr14:75988343
|
C | T | 42 | a0001c0001t0001g0003a0001c0001t0001g0020a0001c0001t0001g0023others(39): Show | 43 | HG01074.hp1 HG01081.hp1 HG01175.hp1 others(40): Show |
intron_variant | MODIFIER | c.55-542C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 1/8 | chr14 | 75988343 | ||||||
chr14:75988517
|
CT | C | 324 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(321): Show | 338 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(335): Show |
intron_variant | MODIFIER | c.55-359delT | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr14 | 75988517 | |||||
chr14:75988536
|
T | G | 1 | a0001c0001t0001g0023 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.55-349T>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 1/8 | chr14 | 75988536 | ||||||
chr14:75988868
|
T | C | 2 | a0001c0001t0001g0012a0001c0001t0001g0373 | 3 | HG03491.hp2 HG03492.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.55-17T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 1/8 | chr14 | 75988868 | ||||||
chr14:75989011
|
T | A | 1 | a0001c0001t0001g0317 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.147+34T>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75989011 | ||||||
chr14:75989024
|
T | G | 1 | a0001c0001t0001g0016 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.147+47T>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75989024 | ||||||
chr14:75989038
|
A | G | 1 | a0001c0001t0001g0245 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.147+61A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75989038 | ||||||
chr14:75989066
|
C | T | 6 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0121others(3): Show | 6 | HG00609.hp2 NA18964.hp1 NA18967.hp1 others(3): Show |
intron_variant | MODIFIER | c.147+89C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75989066 | ||||||
chr14:75989090
|
T | C | 2 | a0001c0001t0001g0063a0001c0001t0001g0064 | 2 | NA18953.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.147+113T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75989090 | ||||||
chr14:75989146
|
G | A | 2 | a0001c0001t0001g0012a0001c0001t0001g0373 | 3 | HG03491.hp2 HG03492.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.147+169G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75989146 | ||||||
chr14:75989385
|
A | C | 2 | a0001c0001t0001g0012a0001c0001t0001g0373 | 3 | HG03491.hp2 HG03492.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.147+408A>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75989385 | ||||||
chr14:75989586
|
C | G | 1 | a0001c0001t0001g0120 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.147+609C>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75989586 | ||||||
chr14:75989798
|
C | T | 4 | a0001c0001t0001g0116a0001c0001t0001g0117a0001c0001t0001g0118others(1): Show | 4 | HG02451.hp2 HG02486.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.147+821C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75989798 | ||||||
chr14:75990185
|
G | A | 2 | a0001c0001t0001g0012a0001c0001t0001g0373 | 3 | HG03491.hp2 HG03492.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.147+1208G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75990185 | ||||||
chr14:75990280
|
G | C | 2 | a0001c0001t0001g0012a0001c0001t0001g0373 | 3 | HG03491.hp2 HG03492.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.147+1303G>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75990280 | ||||||
chr14:75990411
|
A | G | 1 | a0001c0001t0001g0244 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.147+1434A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75990411 | ||||||
chr14:75990511
|
T | C | 1 | a0001c0001t0001g0257 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.147+1534T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75990511 | ||||||
chr14:75990625
|
G | A | 2 | a0001c0001t0001g0012a0001c0001t0001g0373 | 3 | HG03491.hp2 HG03492.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.147+1648G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75990625 | ||||||
chr14:75990642
|
C | T | 3 | a0001c0001t0001g0247a0001c0001t0001g0248a0001c0001t0001g0256 | 3 | HG02647.hp2 HG03139.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.147+1665C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75990642 | ||||||
chr14:75990678
|
G | A | 7 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0368others(4): Show | 7 | HG01109.hp2 HG02486.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.147+1701G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75990678 | ||||||
chr14:75990710
|
A | T | 5 | a0001c0001t0001g0020a0001c0001t0001g0023a0001c0001t0001g0058others(2): Show | 5 | HG01243.hp1 HG01884.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.147+1733A>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75990710 | ||||||
chr14:75991171
|
T | C | 1 | a0001c0001t0001g0318 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.147+2194T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75991171 | ||||||
chr14:75991262
|
C | T | 4 | a0001c0001t0001g0013a0001c0001t0001g0114a0001c0001t0001g0115others(1): Show | 4 | HG02055.hp1 HG02280.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.147+2285C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75991262 | ||||||
chr14:75991359
|
T | TTA | 3 | a0001c0001t0001g0246a0001c0001t0001g0247a0001c0001t0001g0248 | 3 | HG02258.hp1 HG02647.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.147+2397_147+2398d others(4): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 75991359 | |||||
chr14:75991359
|
T | TTATA | 7 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0368others(4): Show | 7 | HG01109.hp2 HG02486.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.147+2395_147+2398d others(6): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 75991359 | |||||
chr14:75991359
|
TTA | T | 3 | a0001c0001t0001g0012a0001c0001t0001g0373a0002c0002t0001g0319 | 4 | HG02155.hp2 HG03491.hp2 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.147+2397_147+2398d others(4): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 75991359 | |||||
chr14:75991388
|
A | AGT | 16 | a0001c0001t0001g0057a0001c0001t0001g0232a0001c0001t0001g0233others(13): Show | 16 | HG01070.hp1 HG01071.hp2 HG01192.hp2 others(13): Show |
intron_variant | MODIFIER | c.147+2448_147+2449d others(4): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 75991388 | |||||
chr14:75991388
|
A | AGTGT | 9 | a0001c0001t0001g0113a0001c0001t0001g0243a0001c0001t0001g0314others(6): Show | 9 | HG02027.hp2 HG02155.hp2 HG02738.hp2 others(6): Show |
intron_variant | MODIFIER | c.147+2446_147+2449d others(6): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 75991388 | |||||
chr14:75991388
|
A | AGTGTGT | 6 | a0001c0001t0001g0002a0001c0001t0001g0315a0001c0001t0001g0316others(3): Show | 8 | HG02056.hp2 HG03017.hp1 NA18940.hp1 others(5): Show |
intron_variant | MODIFIER | c.147+2444_147+2449d others(8): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 75991388 | |||||
chr14:75991388
|
A | AGTGTGTG others(19): Show |
1 | a0001c0001t0001g0256 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.147+2423_147+2424i others(28): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 75991388 | |||||
chr14:75991388
|
A | AGTGTGTG others(23): Show |
1 | a0001c0001t0001g0066 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.147+2423_147+2424i others(32): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 75991388 | |||||
chr14:75991388
|
AGT | A | 92 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0006others(89): Show | 99 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(96): Show |
intron_variant | MODIFIER | c.147+2448_147+2449d others(4): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 75991388 | |||||
chr14:75991388
|
AGTGT | A | 30 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0012others(27): Show | 33 | HG00408.hp2 HG00597.hp1 HG00642.hp2 others(30): Show |
intron_variant | MODIFIER | c.147+2446_147+2449d others(6): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 75991388 | |||||
chr14:75991388
|
AGTGTGT | A | 107 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(104): Show | 110 | HG00609.hp2 HG00673.hp1 HG00741.hp1 others(107): Show |
intron_variant | MODIFIER | c.147+2444_147+2449d others(8): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 75991388 | |||||
chr14:75991388
|
AGTGTGTG others(1): Show |
A | 10 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0072others(7): Show | 10 | HG00099.hp1 HG00733.hp1 HG01081.hp2 others(7): Show |
intron_variant | MODIFIER | c.147+2442_147+2449d others(10): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 75991388 | |||||
chr14:75991388
|
AGTGTGTG others(3): Show |
A | 4 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0320others(1): Show | 4 | HG00735.hp1 HG02148.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.147+2440_147+2449d others(12): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 75991388 | |||||
chr14:75991388
|
AGTGTGTG others(5): Show |
A | 2 | a0001c0001t0001g0067a0001c0001t0001g0068 | 2 | NA18985.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.147+2438_147+2449d others(14): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 75991388 | |||||
chr14:75991390
|
T | TGTGTGTG others(15): Show |
8 | a0001c0001t0001g0013a0001c0001t0001g0015a0001c0001t0001g0020others(5): Show | 8 | HG01243.hp1 HG01884.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.147+2423_147+2424i others(24): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 75991390 | |||||
chr14:75991392
|
T | TGTGTGTG others(13): Show |
5 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0058others(2): Show | 5 | HG02258.hp1 HG02280.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.147+2423_147+2424i others(22): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 75991392 | |||||
chr14:75991394
|
T | A | 1 | a0001c0001t0001g0134 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.147+2417T>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75991394 | ||||||
chr14:75991394
|
T | TGTGTGTA others(11): Show |
4 | a0001c0001t0001g0065a0001c0001t0001g0247a0001c0001t0001g0248others(1): Show | 4 | HG02055.hp1 HG02622.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.147+2423_147+2424i others(20): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 75991394 | |||||
chr14:75991396
|
T | TGTGTATA others(9): Show |
5 | a0001c0001t0001g0368a0001c0001t0001g0369a0001c0001t0001g0370others(2): Show | 5 | HG01109.hp2 HG02486.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.147+2423_147+2424i others(18): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 75991396 | |||||
chr14:75991423
|
G | A | 2 | a0001c0001t0001g0069a0001c0001t0001g0171 | 2 | HG01192.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.147+2446G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75991423 | ||||||
chr14:75991423
|
G | GTGTGTGT others(1): Show |
3 | a0001c0001t0001g0240a0001c0001t0001g0241a0001c0001t0001g0242 | 3 | HG00280.hp2 HG00733.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.147+2449_147+2450i others(10): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 75991423 | |||||
chr14:75991427
|
A | G | 5 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0370others(2): Show | 5 | HG02723.hp2 HG03139.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.147+2450A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75991427 | ||||||
chr14:75991433
|
G | A | 3 | a0001c0001t0001g0240a0001c0001t0001g0241a0001c0001t0001g0242 | 3 | HG00280.hp2 HG00733.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.147+2456G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75991433 | ||||||
chr14:75991516
|
C | G | 2 | a0001c0001t0001g0012a0001c0001t0001g0373 | 3 | HG03491.hp2 HG03492.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.147+2539C>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75991516 | ||||||
chr14:75991738
|
A | G | 7 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0368others(4): Show | 7 | HG01109.hp2 HG02486.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.147+2761A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75991738 | ||||||
chr14:75991883
|
C | T | 23 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0112others(20): Show | 29 | HG01256.hp2 HG01943.hp2 HG01952.hp1 others(26): Show |
intron_variant | MODIFIER | c.147+2906C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75991883 | ||||||
chr14:75992008
|
C | T | 1 | a0001c0001t0001g0015 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.147+3031C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75992008 | ||||||
chr14:75992049
|
C | T | 1 | a0001c0004t0001g0231 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.147+3072C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75992049 | ||||||
chr14:75992050
|
G | A | 1 | a0001c0001t0001g0018 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.147+3073G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75992050 | ||||||
chr14:75992123
|
A | G | 1 | a0001c0001t0001g0284 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.147+3146A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75992123 | ||||||
chr14:75992242
|
A | G | 1 | a0001c0001t0001g0288 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.147+3265A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75992242 | ||||||
chr14:75992304
|
T | C | 2 | a0001c0001t0001g0012a0001c0001t0001g0373 | 3 | HG03491.hp2 HG03492.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.147+3327T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75992304 | ||||||
chr14:75992307
|
G | C | 2 | a0001c0001t0001g0114a0001c0001t0001g0115 | 2 | HG02280.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.147+3330G>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75992307 | ||||||
chr14:75992321
|
C | T | 2 | a0001c0001t0001g0239a0001c0004t0001g0231 | 2 | HG01934.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.147+3344C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75992321 | ||||||
chr14:75992497
|
ACTC | A | 57 | a0001c0001t0001g0004a0001c0001t0001g0021a0001c0001t0001g0022others(54): Show | 58 | HG00099.hp1 HG00408.hp2 HG00609.hp2 others(55): Show |
intron_variant | MODIFIER | c.147+3521_147+3523d others(5): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75992497 | ||||||
chr14:75992525
|
G | T | 11 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0015others(8): Show | 12 | HG01109.hp2 HG02486.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.147+3548G>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75992525 | ||||||
chr14:75992589
|
A | C | 1 | a0001c0001t0001g0055 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.147+3612A>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75992589 | ||||||
chr14:75992593
|
T | C | 1 | a0001c0001t0001g0066 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.147+3616T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75992593 | ||||||
chr14:75992649
|
G | A | 1 | a0001c0001t0001g0172 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.147+3672G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75992649 | ||||||
chr14:75992878
|
G | C | 1 | a0001c0001t0001g0294 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.147+3901G>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75992878 | ||||||
chr14:75993027
|
A | G | 36 | a0001c0001t0001g0003a0001c0001t0001g0025a0001c0001t0001g0026others(33): Show | 37 | HG01074.hp1 HG01081.hp1 HG01175.hp1 others(34): Show |
intron_variant | MODIFIER | c.147+4050A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75993027 | ||||||
chr14:75993085
|
T | C | 10 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0015others(7): Show | 11 | HG01109.hp2 HG02486.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.147+4108T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75993085 | ||||||
chr14:75993146
|
A | G | 1 | a0001c0001t0001g0165 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.147+4169A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75993146 | ||||||
chr14:75993199
|
G | A | 1 | a0001c0001t0001g0266 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.147+4222G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75993199 | ||||||
chr14:75993229
|
G | T | 10 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0015others(7): Show | 11 | HG01109.hp2 HG02486.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.147+4252G>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75993229 | ||||||
chr14:75993387
|
T | A | 10 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0015others(7): Show | 11 | HG01109.hp2 HG02486.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.147+4410T>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75993387 | ||||||
chr14:75993530
|
A | G | 8 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(5): Show | 8 | HG01109.hp2 HG02486.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.147+4553A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75993530 | ||||||
chr14:75993535
|
A | G | 10 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0015others(7): Show | 11 | HG01109.hp2 HG02486.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.147+4558A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75993535 | ||||||
chr14:75993680
|
C | T | 1 | a0001c0001t0001g0013 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.147+4703C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75993680 | ||||||
chr14:75993817
|
G | A | 8 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(5): Show | 8 | HG01109.hp2 HG02486.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.147+4840G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75993817 | ||||||
chr14:75993997
|
C | G | 1 | a0001c0001t0001g0380 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.147+5020C>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75993997 | ||||||
chr14:75994032
|
T | G | 10 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0015others(7): Show | 11 | HG01109.hp2 HG02486.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.147+5055T>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75994032 | ||||||
chr14:75994103
|
C | CT | 12 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0016others(9): Show | 14 | HG00597.hp1 HG01074.hp1 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.147+5138dupT | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 75994103 | |||||
chr14:75994103
|
C | CTT | 7 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0368others(4): Show | 7 | HG01109.hp2 HG02486.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.147+5137_147+5138d others(4): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 75994103 | |||||
chr14:75994161
|
G | T | 10 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0015others(7): Show | 11 | HG01109.hp2 HG02486.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.147+5184G>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75994161 | ||||||
chr14:75994182
|
G | A | 303 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(300): Show | 311 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(308): Show |
intron_variant | MODIFIER | c.147+5205G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75994182 | ||||||
chr14:75994185
|
T | G | 2 | a0001c0001t0001g0012a0001c0001t0001g0373 | 3 | HG03491.hp2 HG03492.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.147+5208T>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75994185 | ||||||
chr14:75994279
|
C | A | 10 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0015others(7): Show | 11 | HG01109.hp2 HG02486.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.147+5302C>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75994279 | ||||||
chr14:75994291
|
G | A | 1 | a0001c0001t0001g0285 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.147+5314G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75994291 | ||||||
chr14:75994403
|
C | T | 1 | a0001c0001t0001g0230 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.147+5426C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75994403 | ||||||
chr14:75994454
|
A | G | 1 | a0001c0001t0001g0164 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.147+5477A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75994454 | ||||||
chr14:75994546
|
C | T | 1 | a0001c0001t0001g0065 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.147+5569C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75994546 | ||||||
chr14:75994625
|
G | C | 7 | a0001c0001t0001g0074a0001c0001t0001g0092a0001c0001t0001g0093others(4): Show | 7 | HG02109.hp2 HG02572.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.147+5648G>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75994625 | ||||||
chr14:75994638
|
C | G | 1 | a0001c0001t0001g0066 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.147+5661C>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75994638 | ||||||
chr14:75994779
|
G | A | 2 | a0001c0001t0001g0013a0001c0001t0001g0380 | 2 | HG02055.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.147+5802G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75994779 | ||||||
chr14:75995087
|
A | G | 1 | a0001c0001t0001g0242 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.147+6110A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75995087 | ||||||
chr14:75995107
|
T | C | 11 | a0001c0001t0001g0013a0001c0001t0001g0023a0001c0001t0001g0065others(8): Show | 11 | HG01123.hp2 HG01361.hp1 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.147+6130T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75995107 | ||||||
chr14:75995154
|
G | C | 3 | a0001c0001t0001g0246a0001c0001t0001g0247a0001c0001t0001g0248 | 3 | HG02258.hp1 HG02647.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.147+6177G>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75995154 | ||||||
chr14:75995189
|
A | G | 3 | a0001c0001t0001g0013a0001c0001t0001g0256a0001c0001t0001g0380 | 3 | HG02055.hp1 HG02965.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.147+6212A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75995189 | ||||||
chr14:75995433
|
C | G | 2 | a0001c0001t0001g0012a0001c0001t0001g0373 | 3 | HG03491.hp2 HG03492.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.147+6456C>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75995433 | ||||||
chr14:75995491
|
C | T | 47 | a0001c0001t0001g0004a0001c0001t0001g0021a0001c0001t0001g0022others(44): Show | 48 | HG00099.hp1 HG00408.hp2 HG00597.hp2 others(45): Show |
intron_variant | MODIFIER | c.147+6514C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75995491 | ||||||
chr14:75995619
|
C | T | 3 | a0001c0001t0001g0206a0001c0001t0001g0207a0001c0001t0001g0208 | 3 | HG02027.hp1 NA18972.hp2 NA18987.hp2 |
intron_variant | MODIFIER | c.147+6642C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75995619 | ||||||
chr14:75995683
|
T | G | 2 | a0001c0001t0001g0375a0001c0001t0001g0376 | 2 | HG02040.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.147+6706T>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75995683 | ||||||
chr14:75995759
|
C | A | 8 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(5): Show | 8 | HG01109.hp2 HG02486.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.147+6782C>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75995759 | ||||||
chr14:75995904
|
C | G | 1 | a0001c0001t0001g0250 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.147+6927C>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75995904 | ||||||
chr14:75995926
|
C | T | 1 | a0001c0001t0001g0364 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.147+6949C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75995926 | ||||||
chr14:75995954
|
G | C | 1 | a0001c0001t0001g0250 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.147+6977G>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75995954 | ||||||
chr14:75996046
|
T | C | 1 | a0001c0001t0001g0135 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.147+7069T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75996046 | ||||||
chr14:75996142
|
C | T | 1 | a0001c0001t0001g0351 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.147+7165C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75996142 | ||||||
chr14:75996174
|
T | C | 1 | a0001c0001t0001g0256 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.147+7197T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75996174 | ||||||
chr14:75996253
|
C | T | 1 | a0001c0001t0001g0163 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.147+7276C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75996253 | ||||||
chr14:75996392
|
A | G | 2 | a0001c0001t0001g0228a0001c0001t0001g0229 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.147+7415A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75996392 | ||||||
chr14:75996451
|
T | C | 1 | a0001c0001t0001g0257 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.147+7474T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75996451 | ||||||
chr14:75996524
|
T | C | 99 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(96): Show | 102 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.147+7547T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75996524 | ||||||
chr14:75996758
|
T | C | 3 | a0001c0001t0001g0246a0001c0001t0001g0247a0001c0001t0001g0248 | 3 | HG02258.hp1 HG02647.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.147+7781T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75996758 | ||||||
chr14:75996991
|
G | A | 117 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0010others(114): Show | 120 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(117): Show |
intron_variant | MODIFIER | c.147+8014G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75996991 | ||||||
chr14:75997152
|
A | T | 1 | a0001c0001t0001g0135 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.147+8175A>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75997152 | ||||||
chr14:75997175
|
GAC | G | 7 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0368others(4): Show | 7 | HG01109.hp2 HG02486.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.147+8200_147+8201d others(4): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 75997175 | |||||
chr14:75997179
|
A | T | 7 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0368others(4): Show | 7 | HG01109.hp2 HG02486.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.147+8202A>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75997179 | ||||||
chr14:75997211
|
T | C | 2 | a0001c0001t0001g0012a0001c0001t0001g0373 | 3 | HG03491.hp2 HG03492.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.147+8234T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75997211 | ||||||
chr14:75997334
|
C | A | 2 | a0001c0001t0001g0012a0001c0001t0001g0373 | 3 | HG03491.hp2 HG03492.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.147+8357C>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75997334 | ||||||
chr14:75997357
|
A | G | 17 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0091others(14): Show | 17 | HG00597.hp2 HG00609.hp2 HG00735.hp1 others(14): Show |
intron_variant | MODIFIER | c.147+8380A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75997357 | ||||||
chr14:75997851
|
T | G | 1 | a0001c0001t0001g0016 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.147+8874T>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75997851 | ||||||
chr14:75997884
|
T | TTGTAAAA others(3): Show |
2 | a0001c0001t0001g0114a0001c0001t0001g0115 | 2 | HG02280.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.147+8912_147+8921d others(12): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 75997884 | |||||
chr14:75997943
|
T | G | 2 | a0001c0001t0001g0013a0001c0001t0001g0380 | 2 | HG02055.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.147+8966T>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75997943 | ||||||
chr14:75997972
|
C | A | 2 | a0001c0001t0001g0012a0001c0001t0001g0373 | 3 | HG03491.hp2 HG03492.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.147+8995C>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75997972 | ||||||
chr14:75998135
|
G | C | 1 | a0001c0001t0001g0126 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.147+9158G>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75998135 | ||||||
chr14:75998211
|
C | G | 1 | a0001c0001t0001g0162 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.147+9234C>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75998211 | ||||||
chr14:75998220
|
T | G | 99 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(96): Show | 102 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.147+9243T>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75998220 | ||||||
chr14:75998299
|
G | T | 2 | a0001c0001t0001g0012a0001c0001t0001g0373 | 3 | HG03491.hp2 HG03492.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.147+9322G>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75998299 | ||||||
chr14:75998488
|
T | C | 165 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(162): Show | 169 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(166): Show |
intron_variant | MODIFIER | c.147+9511T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75998488 | ||||||
chr14:75998489
|
G | A | 1 | a0001c0001t0001g0256 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.147+9512G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75998489 | ||||||
chr14:75998522
|
G | A | 15 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0015others(12): Show | 16 | HG01109.hp2 HG02258.hp1 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.147+9545G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75998522 | ||||||
chr14:75998648
|
A | G | 1 | a0001c0001t0001g0049 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.147+9671A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75998648 | ||||||
chr14:75998702
|
G | A | 1 | a0001c0001t0001g0173 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.147+9725G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75998702 | ||||||
chr14:75998827
|
G | A | 2 | a0001c0001t0001g0113a0001c0001t0001g0269 | 2 | HG01167.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.147+9850G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75998827 | ||||||
chr14:75998944
|
G | A | 2 | a0001c0001t0001g0012a0001c0001t0001g0373 | 3 | HG03491.hp2 HG03492.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.147+9967G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75998944 | ||||||
chr14:75998988
|
G | T | 5 | a0001c0001t0001g0295a0001c0001t0001g0296a0001c0001t0001g0297others(2): Show | 5 | HG00438.hp2 HG02071.hp1 NA18940.hp1 others(2): Show |
intron_variant | MODIFIER | c.147+10011G>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75998988 | ||||||
chr14:75999037
|
G | A | 46 | a0001c0001t0001g0004a0001c0001t0001g0021a0001c0001t0001g0022others(43): Show | 47 | HG00099.hp1 HG00408.hp2 HG00597.hp2 others(44): Show |
intron_variant | MODIFIER | c.147+10060G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75999037 | ||||||
chr14:75999089
|
T | C | 4 | a0001c0001t0001g0009a0001c0001t0001g0105a0001c0001t0001g0251others(1): Show | 5 | HG01891.hp2 HG02976.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.147+10112T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75999089 | ||||||
chr14:75999120
|
G | A | 2 | a0001c0001t0001g0012a0001c0001t0001g0373 | 3 | HG03491.hp2 HG03492.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.147+10143G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75999120 | ||||||
chr14:75999186
|
C | T | 2 | a0001c0001t0001g0012a0001c0001t0001g0373 | 3 | HG03491.hp2 HG03492.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.147+10209C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75999186 | ||||||
chr14:75999225
|
TTTTATAT others(3): Show |
T | 1 | a0001c0001t0001g0101 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.147+10250_147+1025 others(14): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 75999225 | |||||
chr14:75999226
|
T | A | 1 | a0001c0001t0001g0116 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.147+10249T>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75999226 | ||||||
chr14:75999226
|
T | TTATATAT others(30): Show |
1 | a0001c0001t0001g0026 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.147+10250_147+1025 others(41): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 75999226 | |||||
chr14:75999227
|
T | TATATATA others(36): Show |
1 | a0001c0001t0001g0025 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.147+10250_147+1025 others(47): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75999227 | ||||||
chr14:75999227
|
TTA | T | 12 | a0001c0001t0001g0305a0001c0001t0001g0306a0001c0001t0001g0341others(9): Show | 12 | HG00408.hp1 HG00673.hp2 HG01255.hp1 others(9): Show |
intron_variant | MODIFIER | c.147+10294_147+1029 others(6): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 75999227 | |||||
chr14:75999227
|
TTATA | T | 7 | a0001c0001t0001g0018a0001c0001t0001g0066a0001c0001t0001g0292others(4): Show | 7 | HG00597.hp1 HG02109.hp1 HG02165.hp2 others(4): Show |
intron_variant | MODIFIER | c.147+10292_147+1029 others(8): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 75999227 | |||||
chr14:75999227
|
TTATATA | T | 3 | a0001c0001t0001g0308a0001c0001t0001g0350a0001c0001t0001g0363 | 3 | NA18986.hp1 NA18986.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.147+10290_147+1029 others(10): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 75999227 | |||||
chr14:75999227
|
TTATATAT others(13): Show |
T | 1 | a0001c0001t0001g0015 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.147+10276_147+1029 others(24): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 75999227 | |||||
chr14:75999229
|
A | ATATATAT others(31): Show |
1 | a0001c0001t0001g0028 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.147+10264_147+1026 others(42): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 75999229 | |||||
chr14:75999229
|
A | T | 1 | a0001c0001t0001g0026 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.147+10252A>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75999229 | ||||||
chr14:75999230
|
T | C | 1 | a0001c0001t0001g0374 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.147+10253T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75999230 | ||||||
chr14:75999231
|
A | ATATATAT others(27): Show |
1 | a0001c0001t0001g0027 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.147+10262_147+1026 others(38): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 75999231 | |||||
chr14:75999231
|
A | ATATATAT others(29): Show |
1 | a0001c0001t0001g0057 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.147+10264_147+1026 others(40): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 75999231 | |||||
chr14:75999233
|
A | ATATATAT others(27): Show |
4 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0031others(1): Show | 4 | HG01081.hp1 HG02630.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.147+10264_147+1026 others(38): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 75999233 | |||||
chr14:75999235
|
A | ATATATAA others(25): Show |
2 | a0001c0001t0001g0032a0001c0001t0001g0050 | 2 | HG02970.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.147+10264_147+1026 others(36): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 75999235 | |||||
chr14:75999235
|
A | ATATATAT others(27): Show |
1 | a0001c0001t0001g0108 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.147+10266_147+1026 others(38): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 75999235 | |||||
chr14:75999237
|
A | ATATAATA others(6): Show |
1 | a0001c0001t0001g0215 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.147+10264_147+1026 others(17): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 75999237 | |||||
chr14:75999237
|
A | ATATAATA others(23): Show |
6 | a0001c0001t0001g0003a0001c0001t0001g0051a0001c0001t0001g0052others(3): Show | 7 | HG01074.hp1 HG01243.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.147+10264_147+1026 others(34): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 75999237 | |||||
chr14:75999237
|
A | ATATATAA others(25): Show |
3 | a0001c0001t0001g0109a0001c0001t0001g0218a0001c0001t0001g0289 | 3 | HG01358.hp1 HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.147+10266_147+1026 others(36): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 75999237 | |||||
chr14:75999239
|
A | ATAATATT others(4): Show |
2 | a0001c0001t0001g0042a0001c0001t0001g0055 | 2 | HG02015.hp1 NA18952.hp2 |
intron_variant | MODIFIER | c.147+10264_147+1026 others(15): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 75999239 | |||||
chr14:75999239
|
A | ATAATATT others(21): Show |
1 | a0001c0001t0001g0034 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.147+10264_147+1026 others(32): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 75999239 | |||||
chr14:75999239
|
A | ATATAATA others(6): Show |
1 | a0001c0001t0001g0220 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.147+10266_147+1026 others(17): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 75999239 | |||||
chr14:75999239
|
A | ATATAATA others(23): Show |
2 | a0001c0001t0001g0216a0001c0001t0001g0217 | 2 | HG02004.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.147+10266_147+1026 others(34): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 75999239 | |||||
chr14:75999241
|
A | AATATTCA others(2): Show |
6 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0045others(3): Show | 6 | HG01175.hp1 HG01928.hp2 HG01943.hp1 others(3): Show |
intron_variant | MODIFIER | c.147+10264_147+1026 others(13): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75999241 | ||||||
chr14:75999241
|
A | AATATTCA others(17): Show |
6 | a0001c0001t0001g0035a0001c0001t0001g0037a0001c0001t0001g0038others(3): Show | 6 | NA18960.hp1 NA18963.hp1 NA18991.hp2 others(3): Show |
intron_variant | MODIFIER | c.147+10264_147+1026 others(28): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75999241 | ||||||
chr14:75999241
|
A | AATATTCA others(19): Show |
2 | a0001c0001t0001g0036a0001c0001t0001g0056 | 2 | HG02818.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.147+10264_147+1026 others(30): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75999241 | ||||||
chr14:75999241
|
A | ATAATATT others(4): Show |
12 | a0001c0001t0001g0017a0001c0001t0001g0204a0001c0001t0001g0226others(9): Show | 12 | HG01517.hp1 HG02055.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.147+10266_147+1026 others(15): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 75999241 | |||||
chr14:75999241
|
A | ATAATATT others(21): Show |
3 | a0001c0001t0001g0228a0001c0001t0001g0229a0001c0001t0001g0240 | 3 | HG00280.hp2 HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.147+10266_147+1026 others(32): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 75999241 | |||||
chr14:75999243
|
A | AATATTCA others(2): Show |
36 | a0001c0001t0001g0010a0001c0001t0001g0063a0001c0001t0001g0064others(33): Show | 37 | HG00438.hp2 HG00642.hp2 HG01070.hp1 others(34): Show |
intron_variant | MODIFIER | c.147+10266_147+1026 others(13): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75999243 | ||||||
chr14:75999243
|
A | AATATTCA others(17): Show |
11 | a0001c0001t0001g0201a0001c0001t0001g0202a0001c0001t0001g0203others(8): Show | 11 | HG00099.hp2 HG01934.hp2 HG02735.hp2 others(8): Show |
intron_variant | MODIFIER | c.147+10266_147+1026 others(28): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75999243 | ||||||
chr14:75999243
|
A | AATATTCA others(19): Show |
8 | a0001c0001t0001g0135a0001c0001t0001g0219a0001c0001t0001g0222others(5): Show | 8 | HG00423.hp2 HG00733.hp2 HG01168.hp1 others(5): Show |
intron_variant | MODIFIER | c.147+10266_147+1026 others(30): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75999243 | ||||||
chr14:75999243
|
A | T | 6 | a0001c0001t0001g0035a0001c0001t0001g0037a0001c0001t0001g0038others(3): Show | 6 | NA18960.hp1 NA18963.hp1 NA18991.hp2 others(3): Show |
intron_variant | MODIFIER | c.147+10266A>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75999243 | ||||||
chr14:75999243
|
ATATATAT others(32): Show |
A | 1 | a0001c0001t0001g0140 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.147+10268_147+1030 others(43): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 75999243 | |||||
chr14:75999245
|
A | T | 12 | a0001c0001t0001g0048a0001c0001t0001g0201a0001c0001t0001g0202others(9): Show | 12 | HG00099.hp2 HG01934.hp2 HG02300.hp2 others(9): Show |
intron_variant | MODIFIER | c.147+10268A>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75999245 | ||||||
chr14:75999245
|
ATATATAT others(32): Show |
A | 31 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0117others(28): Show | 32 | HG00423.hp1 HG00438.hp1 HG00609.hp1 others(29): Show |
intron_variant | MODIFIER | c.147+10270_147+1030 others(43): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 75999245 | |||||
chr14:75999245
|
ATATATAT others(33): Show |
A | 2 | a0001c0001t0001g0184a0001c0001t0001g0185 | 2 | NA19056.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.147+10270_147+1030 others(44): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 75999245 | |||||
chr14:75999246
|
T | C | 1 | a0001c0001t0001g0048 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.147+10269T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75999246 | ||||||
chr14:75999247
|
A | AAATTCAT others(2): Show |
3 | a0001c0001t0001g0042a0001c0001t0001g0055a0001c0001t0001g0220 | 3 | HG02015.hp1 HG02165.hp1 NA18952.hp2 |
intron_variant | MODIFIER | c.147+10270_147+1027 others(13): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75999247 | ||||||
chr14:75999247
|
A | T | 1 | a0001c0001t0001g0047 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.147+10270A>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75999247 | ||||||
chr14:75999247
|
ATATATAT others(19): Show |
A | 1 | a0001c0001t0001g0287 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.147+10280_147+1030 others(30): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 75999247 | |||||
chr14:75999247
|
ATATATAT others(31): Show |
A | 1 | a0001c0001t0001g0130 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.147+10272_147+1030 others(42): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 75999247 | |||||
chr14:75999247
|
ATATATAT others(32): Show |
A | 49 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0019others(46): Show | 51 | HG00280.hp1 HG00741.hp1 HG01070.hp2 others(48): Show |
intron_variant | MODIFIER | c.147+10272_147+1031 others(43): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 75999247 | |||||
chr14:75999247
|
ATATATAT others(33): Show |
A | 2 | a0001c0001t0001g0134a0001c0001t0001g0175 | 2 | HG01496.hp2 HG02015.hp2 |
intron_variant | MODIFIER | c.147+10272_147+1031 others(44): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 75999247 | |||||
chr14:75999248
|
TATATATA others(16): Show |
T | 4 | a0001c0001t0001g0368a0001c0001t0001g0369a0001c0001t0001g0371others(1): Show | 4 | HG01109.hp2 HG02486.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.147+10272_147+1029 others(27): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75999248 | ||||||
chr14:75999249
|
A | AAATTCAT others(2): Show |
17 | a0001c0001t0001g0017a0001c0001t0001g0043a0001c0001t0001g0044others(14): Show | 17 | HG01175.hp1 HG01517.hp1 HG01928.hp2 others(14): Show |
intron_variant | MODIFIER | c.147+10272_147+1027 others(13): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75999249 | ||||||
chr14:75999249
|
A | AAATTCAT others(4): Show |
1 | a0001c0001t0001g0281 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.147+10272_147+1027 others(15): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75999249 | ||||||
chr14:75999249
|
A | G | 6 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0294others(3): Show | 12 | HG01256.hp2 HG01943.hp2 HG01952.hp1 others(9): Show |
intron_variant | MODIFIER | c.147+10272A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75999249 | ||||||
chr14:75999249
|
A | T | 1 | a0001c0001t0001g0048 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.147+10272A>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75999249 | ||||||
chr14:75999249
|
ATATATAT others(17): Show |
A | 1 | a0001c0001t0001g0065 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.147+10282_147+1030 others(28): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 75999249 | |||||
chr14:75999249
|
ATATATAT others(31): Show |
A | 3 | a0001c0001t0001g0125a0001c0001t0001g0129a0001c0001t0001g0206 | 3 | HG02027.hp1 NA18967.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.147+10274_147+1031 others(42): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 75999249 | |||||
chr14:75999249
|
ATATATAT others(32): Show |
A | 6 | a0001c0001t0001g0126a0001c0001t0001g0128a0001c0001t0001g0141others(3): Show | 6 | HG00642.hp1 HG00735.hp2 HG01069.hp2 others(3): Show |
intron_variant | MODIFIER | c.147+10274_147+1031 others(43): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 75999249 | |||||
chr14:75999250
|
TATATATA others(14): Show |
T | 1 | a0001c0001t0001g0014 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.147+10274_147+1029 others(25): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75999250 | ||||||
chr14:75999251
|
A | AAATTCAT others(2): Show |
34 | a0001c0001t0001g0010a0001c0001t0001g0063a0001c0001t0001g0064others(31): Show | 35 | HG00642.hp2 HG01070.hp1 HG01071.hp2 others(32): Show |
intron_variant | MODIFIER | c.147+10274_147+1027 others(13): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75999251 | ||||||
chr14:75999251
|
ATATATAT others(15): Show |
A | 1 | a0001c0001t0001g0370 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.147+10284_147+1030 others(26): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 75999251 | |||||
chr14:75999251
|
ATATATAT others(32): Show |
A | 1 | a0001c0001t0001g0209 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.147+10276_147+1031 others(43): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 75999251 | |||||
chr14:75999252
|
TATATATA others(16): Show |
T | 1 | a0001c0001t0001g0256 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.147+10276_147+1029 others(27): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75999252 | ||||||
chr14:75999253
|
A | T | 2 | a0001c0001t0001g0282a0001c0001t0001g0297 | 2 | HG00438.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.147+10276A>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75999253 | ||||||
chr14:75999253
|
ATATATAT others(13): Show |
A | 5 | a0001c0001t0001g0009a0001c0001t0001g0105a0001c0001t0001g0253others(2): Show | 6 | HG01891.hp2 HG02615.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.147+10286_147+1030 others(24): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 75999253 | |||||
chr14:75999253
|
ATATATAT others(24): Show |
A | 2 | a0001c0001t0001g0012a0001c0001t0001g0373 | 3 | HG03491.hp2 HG03492.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.147+10278_147+1030 others(35): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 75999253 | |||||
chr14:75999255
|
ATATATAT others(11): Show |
A | 6 | a0001c0001t0001g0074a0001c0001t0001g0094a0001c0001t0001g0095others(3): Show | 6 | HG02572.hp1 HG02922.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.147+10288_147+1030 others(22): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 75999255 | |||||
chr14:75999256
|
TATATATA others(14): Show |
T | 2 | a0001c0001t0001g0251a0001c0001t0001g0252 | 2 | HG03130.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.147+10280_147+1030 others(25): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75999256 | ||||||
chr14:75999257
|
A | G | 1 | a0001c0001t0001g0106 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.147+10280A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75999257 | ||||||
chr14:75999257
|
ATATATAT others(18): Show |
A | 5 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0294others(2): Show | 11 | HG01256.hp2 HG01943.hp2 HG01952.hp1 others(8): Show |
intron_variant | MODIFIER | c.147+10282_147+1030 others(29): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 75999257 | |||||
chr14:75999257
|
ATATATAT others(19): Show |
A | 1 | a0001c0001t0001g0316 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.147+10282_147+1030 others(30): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 75999257 | |||||
chr14:75999259
|
ATATATAT others(7): Show |
A | 2 | a0001c0001t0001g0060a0001c0001t0001g0082 | 2 | HG02647.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.147+10292_147+1030 others(18): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 75999259 | |||||
chr14:75999259
|
ATATATAT others(18): Show |
A | 1 | a0001c0001t0001g0380 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.147+10284_147+1030 others(29): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 75999259 | |||||
chr14:75999259
|
ATATATAT others(23): Show |
A | 1 | a0001c0001t0001g0023 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.147+10284_147+1031 others(34): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 75999259 | |||||
chr14:75999260
|
TATATATA others(14): Show |
T | 1 | a0001c0001t0001g0114 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.147+10284_147+1030 others(25): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75999260 | ||||||
chr14:75999261
|
ATATATAT others(5): Show |
A | 6 | a0001c0001t0001g0016a0001c0001t0001g0061a0001c0001t0001g0083others(3): Show | 6 | HG01361.hp2 HG02559.hp2 HG02602.hp2 others(3): Show |
intron_variant | MODIFIER | c.147+10294_147+1030 others(16): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 75999261 | |||||
chr14:75999262
|
TATATATA others(12): Show |
T | 1 | a0001c0001t0001g0098 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.147+10286_147+1030 others(23): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75999262 | ||||||
chr14:75999263
|
A | G | 1 | a0001c0001t0001g0293 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.147+10286A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75999263 | ||||||
chr14:75999263
|
ATATATAT others(3): Show |
A | 3 | a0001c0001t0001g0079a0001c0001t0001g0250a0001c0001t0001g0324 | 3 | HG02717.hp1 HG02735.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.147+10296_147+1030 others(14): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 75999263 | |||||
chr14:75999263
|
ATATATAT others(12): Show |
A | 1 | a0001c0001t0001g0093 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.147+10288_147+1030 others(23): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 75999263 | |||||
chr14:75999264
|
TATATATA others(8): Show |
T | 2 | a0001c0001t0001g0024a0001c0001t0001g0081 | 2 | HG02451.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.147+10288_147+1030 others(19): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75999264 | ||||||
chr14:75999265
|
A | G | 1 | a0001c0001t0001g0299 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.147+10288A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75999265 | ||||||
chr14:75999265
|
ATATATAT others(1): Show |
A | 9 | a0001c0001t0001g0022a0001c0001t0001g0073a0001c0001t0001g0077others(6): Show | 9 | HG01175.hp2 HG01981.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.147+10296_147+1030 others(12): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 75999265 | |||||
chr14:75999265
|
ATATATAT others(10): Show |
A | 1 | a0001c0001t0001g0106 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.147+10290_147+1030 others(21): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 75999265 | |||||
chr14:75999265
|
ATATATAT others(11): Show |
A | 1 | a0001c0001t0001g0092 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.147+10290_147+1030 others(22): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 75999265 | |||||
chr14:75999266
|
TATATATG others(8): Show |
T | 1 | a0001c0001t0001g0080 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.147+10290_147+1030 others(19): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75999266 | ||||||
chr14:75999267
|
ATATATG | A | 6 | a0001c0001t0001g0072a0001c0001t0001g0088a0001c0001t0001g0089others(3): Show | 6 | HG00597.hp2 HG00733.hp1 HG01106.hp1 others(3): Show |
intron_variant | MODIFIER | c.147+10296_147+1030 others(10): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 75999267 | |||||
chr14:75999267
|
ATATATGT others(8): Show |
A | 1 | a0001c0001t0001g0115 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.147+10292_147+1030 others(19): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 75999267 | |||||
chr14:75999267
|
ATATATGT others(11): Show |
A | 1 | a0001c0001t0001g0020 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.147+10292_147+1030 others(22): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 75999267 | |||||
chr14:75999268
|
TATATGTA others(4): Show |
T | 1 | a0001c0001t0001g0090 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.147+10292_147+1030 others(15): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75999268 | ||||||
chr14:75999269
|
A | G | 3 | a0001c0001t0001g0283a0001c0001t0001g0347a0001c0001t0001g0348 | 3 | HG03831.hp2 NA18522.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.147+10292A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75999269 | ||||||
chr14:75999269
|
ATATG | A | 6 | a0001c0001t0001g0004a0001c0001t0001g0058a0001c0001t0001g0062others(3): Show | 7 | HG01069.hp1 HG01071.hp1 HG01891.hp1 others(4): Show |
intron_variant | MODIFIER | c.147+10296_147+1029 others(8): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 75999269 | |||||
chr14:75999270
|
TATGTATA others(4): Show |
T | 1 | a0001c0001t0001g0013 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.147+10294_147+1030 others(15): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75999270 | ||||||
chr14:75999271
|
A | G | 1 | a0001c0001t0001g0355 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.147+10294A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75999271 | ||||||
chr14:75999271
|
A | T | 1 | a0001c0001t0001g0015 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.147+10294A>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75999271 | ||||||
chr14:75999271
|
ATG | A | 5 | a0001c0001t0001g0021a0001c0001t0001g0120a0001c0001t0001g0121others(2): Show | 5 | HG00609.hp2 HG03834.hp1 NA18983.hp2 others(2): Show |
intron_variant | MODIFIER | c.147+10296_147+1029 others(6): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 75999271 | |||||
chr14:75999271
|
ATGTATAT others(4): Show |
A | 1 | a0001c0001t0001g0293 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.147+10296_147+1030 others(15): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 75999271 | |||||
chr14:75999273
|
G | A | 147 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0017others(144): Show | 149 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(146): Show |
intron_variant | MODIFIER | c.147+10296G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75999273 | ||||||
chr14:75999273
|
G | T | 8 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0086others(5): Show | 8 | HG01109.hp2 HG02135.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.147+10296G>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75999273 | ||||||
chr14:75999274
|
TATATATA | T | 3 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0085 | 3 | HG00099.hp1 HG00741.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.147+10298_147+1030 others(11): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75999274 | ||||||
chr14:75999275
|
A | G | 5 | a0001c0001t0001g0302a0001c0001t0001g0352a0001c0001t0001g0377others(2): Show | 5 | NA18950.hp1 NA18978.hp1 NA18995.hp1 others(2): Show |
intron_variant | MODIFIER | c.147+10298A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75999275 | ||||||
chr14:75999275
|
A | T | 11 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0068others(8): Show | 11 | HG01109.hp2 HG02135.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.147+10298A>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75999275 | ||||||
chr14:75999275
|
ATATATAT others(4): Show |
A | 1 | a0001c0001t0001g0263 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.147+10300_147+1031 others(15): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 75999275 | |||||
chr14:75999275
|
ATATATAT others(5): Show |
A | 1 | a0001c0001t0001g0059 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.147+10300_147+1031 others(16): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 75999275 | |||||
chr14:75999277
|
A | ATTT | 3 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0001g0049 | 3 | HG01175.hp1 HG01943.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.147+10301_147+1030 others(7): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 75999277 | |||||
chr14:75999277
|
A | G | 4 | a0001c0001t0001g0328a0001c0001t0001g0332a0001c0001t0001g0333others(1): Show | 4 | NA18998.hp1 NA19057.hp1 NA19084.hp1 others(1): Show |
intron_variant | MODIFIER | c.147+10300A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75999277 | ||||||
chr14:75999277
|
A | T | 26 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0015others(23): Show | 27 | HG01106.hp1 HG01109.hp2 HG01361.hp2 others(24): Show |
intron_variant | MODIFIER | c.147+10300A>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75999277 | ||||||
chr14:75999278
|
TA | T | 3 | a0001c0001t0001g0056a0001c0001t0001g0280a0001c0001t0001g0288 | 3 | HG01884.hp1 HG03927.hp2 NA18947.hp1 |
intron_variant | MODIFIER | c.147+10302delA | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75999278 | ||||||
chr14:75999279
|
A | G | 3 | a0001c0001t0001g0300a0001c0001t0001g0301a0002c0002t0001g0362 | 3 | HG02056.hp2 NA18612.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.147+10302A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75999279 | ||||||
chr14:75999279
|
A | T | 47 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0015others(44): Show | 48 | HG00597.hp2 HG01106.hp1 HG01109.hp2 others(45): Show |
intron_variant | MODIFIER | c.147+10302A>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75999279 | ||||||
chr14:75999280
|
TA | T | 8 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041others(5): Show | 8 | HG01934.hp2 HG03139.hp2 HG03710.hp2 others(5): Show |
intron_variant | MODIFIER | c.147+10304delA | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75999280 | ||||||
chr14:75999281
|
A | ATTTTTTT others(3): Show |
2 | a0001c0001t0001g0108a0001c0001t0001g0289 | 2 | HG01517.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.147+10314_147+1032 others(14): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 75999281 | |||||
chr14:75999281
|
A | G | 1 | a0001c0001t0001g0331 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.147+10304A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75999281 | ||||||
chr14:75999281
|
A | T | 77 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0014others(74): Show | 79 | HG00408.hp2 HG00597.hp2 HG00609.hp2 others(76): Show |
intron_variant | MODIFIER | c.147+10304A>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75999281 | ||||||
chr14:75999281
|
AT | A | 46 | a0001c0001t0001g0011a0001c0001t0001g0018a0001c0001t0001g0037others(43): Show | 47 | HG00408.hp1 HG00597.hp1 HG00673.hp2 others(44): Show |
intron_variant | MODIFIER | c.147+10323delT | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 75999281 | |||||
chr14:75999282
|
T | TA | 9 | a0001c0001t0001g0028a0001c0001t0001g0113a0001c0001t0001g0216others(6): Show | 9 | HG00280.hp2 HG02698.hp2 HG02738.hp2 others(6): Show |
intron_variant | MODIFIER | c.147+10305_147+1030 others(5): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75999282 | ||||||
chr14:75999282
|
T | TATA | 4 | a0001c0001t0001g0328a0001c0001t0001g0332a0001c0001t0001g0333others(1): Show | 4 | NA18998.hp1 NA19057.hp1 NA19084.hp1 others(1): Show |
intron_variant | MODIFIER | c.147+10305_147+1030 others(7): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75999282 | ||||||
chr14:75999282
|
T | TATATA | 3 | a0001c0001t0001g0300a0001c0001t0001g0301a0002c0002t0001g0362 | 3 | HG02056.hp2 NA18612.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.147+10305_147+1030 others(9): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75999282 | ||||||
chr14:75999283
|
T | A | 38 | a0001c0001t0001g0025a0001c0001t0001g0029a0001c0001t0001g0030others(35): Show | 38 | HG00099.hp2 HG00642.hp2 HG01070.hp1 others(35): Show |
intron_variant | MODIFIER | c.147+10306T>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75999283 | ||||||
chr14:75999284
|
T | A | 3 | a0001c0001t0001g0335a0001c0001t0001g0361a0002c0002t0001g0356 | 3 | NA18612.hp1 NA18940.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.147+10307T>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75999284 | ||||||
chr14:75999285
|
T | A | 9 | a0001c0001t0001g0025a0001c0001t0001g0029a0001c0001t0001g0220others(6): Show | 9 | HG00642.hp2 HG01081.hp1 HG01261.hp2 others(6): Show |
intron_variant | MODIFIER | c.147+10308T>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75999285 | ||||||
chr14:75999300
|
T | A | 1 | a0001c0001t0001g0016 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.147+10323T>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75999300 | ||||||
chr14:75999342
|
G | A | 3 | a0001c0001t0001g0108a0001c0001t0001g0109a0001c0001t0001g0289 | 3 | HG01516.hp2 HG01517.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.147+10365G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75999342 | ||||||
chr14:75999354
|
C | G | 2 | a0001c0001t0001g0013a0001c0001t0001g0380 | 2 | HG02055.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.147+10377C>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75999354 | ||||||
chr14:75999427
|
A | G | 1 | a0001c0001t0001g0376 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.147+10450A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75999427 | ||||||
chr14:75999697
|
A | C | 1 | a0001c0001t0001g0036 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.147+10720A>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75999697 | ||||||
chr14:75999802
|
G | T | 92 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(89): Show | 95 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.147+10825G>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75999802 | ||||||
chr14:75999995
|
G | T | 2 | a0001c0001t0001g0012a0001c0001t0001g0373 | 3 | HG03491.hp2 HG03492.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.147+11018G>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75999995 | ||||||
chr14:76000044
|
C | T | 1 | a0001c0001t0001g0221 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.147+11067C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76000044 | ||||||
chr14:76000168
|
T | C | 1 | a0001c0001t0001g0042 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.147+11191T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76000168 | ||||||
chr14:76000239
|
T | C | 2 | a0001c0001t0001g0251a0001c0001t0001g0252 | 2 | HG03130.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.147+11262T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76000239 | ||||||
chr14:76000262
|
C | CT | 8 | a0001c0001t0001g0041a0001c0001t0001g0078a0001c0001t0001g0290others(5): Show | 8 | HG00735.hp1 HG01981.hp1 HG02148.hp2 others(5): Show |
intron_variant | MODIFIER | c.147+11305dupT | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 76000262 | |||||
chr14:76000262
|
CT | C | 112 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(109): Show | 116 | HG00280.hp1 HG00438.hp1 HG00642.hp1 others(113): Show |
intron_variant | MODIFIER | c.147+11305delT | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 76000262 | |||||
chr14:76000262
|
CTTTT | C | 17 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(14): Show | 17 | HG01109.hp2 HG02055.hp1 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.147+11302_147+1130 others(8): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 76000262 | |||||
chr14:76000369
|
A | C | 2 | a0001c0001t0001g0013a0001c0001t0001g0380 | 2 | HG02055.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.147+11392A>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76000369 | ||||||
chr14:76000392
|
G | A | 3 | a0001c0001t0001g0215a0001c0001t0001g0228a0001c0001t0001g0229 | 3 | HG01256.hp1 HG01258.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.147+11415G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76000392 | ||||||
chr14:76000402
|
C | A | 7 | a0001c0001t0001g0009a0001c0001t0001g0105a0001c0001t0001g0251others(4): Show | 8 | HG01891.hp2 HG02615.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.147+11425C>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76000402 | ||||||
chr14:76000410
|
G | A | 380 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(377): Show | 395 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(392): Show |
intron_variant | MODIFIER | c.147+11433G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76000410 | ||||||
chr14:76000421
|
C | T | 4 | a0001c0001t0001g0065a0001c0001t0001g0246a0001c0001t0001g0247others(1): Show | 4 | HG02258.hp1 HG02622.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.147+11444C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76000421 | ||||||
chr14:76000431
|
A | AT | 25 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0021others(22): Show | 27 | HG01074.hp1 HG01081.hp1 HG01243.hp2 others(24): Show |
intron_variant | MODIFIER | c.147+11468dupT | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 76000431 | |||||
chr14:76000431
|
AT | A | 17 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(14): Show | 17 | HG01109.hp2 HG02055.hp1 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.147+11468delT | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 76000431 | |||||
chr14:76000474
|
G | A | 8 | a0001c0001t0001g0012a0001c0001t0001g0020a0001c0001t0001g0023others(5): Show | 9 | HG01243.hp1 HG01884.hp2 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.147+11497G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76000474 | ||||||
chr14:76000563
|
C | T | 1 | a0001c0001t0001g0311 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.147+11586C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76000563 | ||||||
chr14:76000680
|
G | T | 1 | a0001c0001t0001g0066 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.147+11703G>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76000680 | ||||||
chr14:76000856
|
C | G | 1 | a0001c0001t0001g0282 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.147+11879C>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76000856 | ||||||
chr14:76001013
|
C | T | 8 | a0001c0001t0001g0012a0001c0001t0001g0020a0001c0001t0001g0023others(5): Show | 9 | HG01243.hp1 HG01884.hp2 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.147+12036C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76001013 | ||||||
chr14:76001147
|
G | C | 5 | a0001c0001t0001g0013a0001c0001t0001g0066a0001c0001t0001g0114others(2): Show | 5 | HG02055.hp1 HG02280.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.147+12170G>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76001147 | ||||||
chr14:76001420
|
G | A | 8 | a0001c0001t0001g0012a0001c0001t0001g0020a0001c0001t0001g0023others(5): Show | 9 | HG01243.hp1 HG01884.hp2 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.147+12443G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76001420 | ||||||
chr14:76001559
|
C | T | 3 | a0001c0001t0001g0108a0001c0001t0001g0109a0001c0001t0001g0289 | 3 | HG01516.hp2 HG01517.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.147+12582C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76001559 | ||||||
chr14:76001634
|
G | A | 92 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(89): Show | 95 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.147+12657G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76001634 | ||||||
chr14:76001892
|
T | G | 5 | a0001c0001t0001g0013a0001c0001t0001g0066a0001c0001t0001g0114others(2): Show | 5 | HG02055.hp1 HG02280.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.147+12915T>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76001892 | ||||||
chr14:76001985
|
T | C | 8 | a0001c0001t0001g0012a0001c0001t0001g0020a0001c0001t0001g0023others(5): Show | 9 | HG01243.hp1 HG01884.hp2 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.147+13008T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76001985 | ||||||
chr14:76002222
|
G | C | 1 | a0001c0001t0001g0102 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.147+13245G>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76002222 | ||||||
chr14:76002299
|
T | C | 92 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(89): Show | 95 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.147+13322T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76002299 | ||||||
chr14:76002336
|
C | T | 42 | a0001c0001t0001g0010a0001c0001t0001g0017a0001c0001t0001g0063others(39): Show | 43 | HG00438.hp2 HG00642.hp2 HG01070.hp1 others(40): Show |
intron_variant | MODIFIER | c.147+13359C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76002336 | ||||||
chr14:76002363
|
G | A | 8 | a0001c0001t0001g0012a0001c0001t0001g0020a0001c0001t0001g0023others(5): Show | 9 | HG01243.hp1 HG01884.hp2 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.147+13386G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76002363 | ||||||
chr14:76002366
|
AG | A | 297 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(294): Show | 304 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(301): Show |
intron_variant | MODIFIER | c.147+13398delG | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 76002366 | |||||
chr14:76002378
|
G | A | 6 | a0001c0001t0001g0020a0001c0001t0001g0023a0001c0001t0001g0024others(3): Show | 6 | HG01243.hp1 HG01884.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.147+13401G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76002378 | ||||||
chr14:76002453
|
G | A | 8 | a0001c0001t0001g0012a0001c0001t0001g0020a0001c0001t0001g0023others(5): Show | 9 | HG01243.hp1 HG01884.hp2 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.147+13476G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76002453 | ||||||
chr14:76002497
|
C | T | 40 | a0001c0001t0001g0003a0001c0001t0001g0025a0001c0001t0001g0026others(37): Show | 41 | HG01074.hp1 HG01081.hp1 HG01175.hp1 others(38): Show |
intron_variant | MODIFIER | c.147+13520C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76002497 | ||||||
chr14:76002535
|
C | T | 1 | a0001c0001t0001g0028 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.147+13558C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76002535 | ||||||
chr14:76002750
|
A | C | 8 | a0001c0001t0001g0012a0001c0001t0001g0020a0001c0001t0001g0023others(5): Show | 9 | HG01243.hp1 HG01884.hp2 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.147+13773A>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76002750 | ||||||
chr14:76002751
|
T | A | 8 | a0001c0001t0001g0012a0001c0001t0001g0020a0001c0001t0001g0023others(5): Show | 9 | HG01243.hp1 HG01884.hp2 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.147+13774T>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76002751 | ||||||
chr14:76002888
|
G | A | 6 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0114others(3): Show | 7 | HG02055.hp1 HG02280.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.147+13911G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76002888 | ||||||
chr14:76002964
|
C | T | 90 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(87): Show | 93 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(90): Show |
intron_variant | MODIFIER | c.147+13987C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76002964 | ||||||
chr14:76003019
|
C | T | 184 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(181): Show | 189 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(186): Show |
intron_variant | MODIFIER | c.147+14042C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76003019 | ||||||
chr14:76003121
|
G | A | 1 | a0001c0001t0001g0016 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.147+14144G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76003121 | ||||||
chr14:76003438
|
C | T | 6 | a0001c0001t0001g0020a0001c0001t0001g0023a0001c0001t0001g0024others(3): Show | 6 | HG01243.hp1 HG01884.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.147+14461C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76003438 | ||||||
chr14:76003647
|
G | A | 8 | a0001c0001t0001g0012a0001c0001t0001g0020a0001c0001t0001g0023others(5): Show | 9 | HG01243.hp1 HG01884.hp2 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.147+14670G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76003647 | ||||||
chr14:76003696
|
C | T | 1 | a0001c0001t0001g0096 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.147+14719C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76003696 | ||||||
chr14:76003772
|
G | A | 6 | a0001c0001t0001g0020a0001c0001t0001g0023a0001c0001t0001g0024others(3): Show | 6 | HG01243.hp1 HG01884.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.147+14795G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76003772 | ||||||
chr14:76004014
|
G | T | 3 | a0001c0001t0001g0157a0001c0001t0001g0158a0001c0001t0001g0164 | 3 | NA18946.hp2 NA18964.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.147+15037G>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76004014 | ||||||
chr14:76004020
|
C | T | 1 | a0001c0001t0001g0071 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.147+15043C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76004020 | ||||||
chr14:76004037
|
A | G | 4 | a0001c0001t0001g0049a0001c0001t0001g0062a0001c0001t0001g0087others(1): Show | 4 | HG01993.hp2 HG02922.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.147+15060A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76004037 | ||||||
chr14:76004066
|
A | G | 2 | a0001c0001t0001g0012a0001c0001t0001g0373 | 3 | HG03491.hp2 HG03492.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.147+15089A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76004066 | ||||||
chr14:76004234
|
A | G | 2 | a0001c0001t0001g0012a0001c0001t0001g0373 | 3 | HG03491.hp2 HG03492.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.147+15257A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76004234 | ||||||
chr14:76004312
|
T | C | 28 | a0001c0001t0001g0135a0001c0001t0001g0201a0001c0001t0001g0202others(25): Show | 28 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(25): Show |
intron_variant | MODIFIER | c.147+15335T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76004312 | ||||||
chr14:76004336
|
G | GT | 7 | a0001c0001t0001g0013a0001c0001t0001g0066a0001c0001t0001g0114others(4): Show | 7 | HG02055.hp1 HG02280.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.147+15369dupT | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 76004336 | |||||
chr14:76004418
|
G | A | 3 | a0001c0001t0001g0116a0001c0001t0001g0117a0001c0001t0001g0118 | 3 | HG02451.hp2 HG02486.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.147+15441G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76004418 | ||||||
chr14:76004485
|
A | G | 1 | a0001c0001t0001g0244 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.147+15508A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76004485 | ||||||
chr14:76004580
|
A | G | 8 | a0001c0001t0001g0012a0001c0001t0001g0020a0001c0001t0001g0023others(5): Show | 9 | HG01243.hp1 HG01884.hp2 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.147+15603A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76004580 | ||||||
chr14:76004589
|
T | C | 1 | a0001c0001t0001g0290 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.147+15612T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76004589 | ||||||
chr14:76005088
|
T | C | 8 | a0001c0001t0001g0012a0001c0001t0001g0020a0001c0001t0001g0023others(5): Show | 9 | HG01243.hp1 HG01884.hp2 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.147+16111T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76005088 | ||||||
chr14:76005128
|
A | G | 3 | a0001c0001t0001g0062a0001c0001t0001g0087a0001c0001t0001g0090 | 3 | HG02922.hp1 HG03209.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.147+16151A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76005128 | ||||||
chr14:76005296
|
G | A | 2 | a0001c0001t0001g0114a0001c0001t0001g0115 | 2 | HG02280.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.147+16319G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76005296 | ||||||
chr14:76005325
|
G | C | 57 | a0001c0001t0001g0004a0001c0001t0001g0021a0001c0001t0001g0022others(54): Show | 58 | HG00099.hp1 HG00408.hp2 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.147+16348G>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76005325 | ||||||
chr14:76005377
|
G | A | 1 | a0001c0001t0001g0066 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.147+16400G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76005377 | ||||||
chr14:76005477
|
A | G | 6 | a0001c0001t0001g0020a0001c0001t0001g0023a0001c0001t0001g0024others(3): Show | 6 | HG01243.hp1 HG01884.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.147+16500A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76005477 | ||||||
chr14:76005497
|
T | C | 1 | a0001c0001t0001g0363 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.147+16520T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76005497 | ||||||
chr14:76005649
|
T | C | 8 | a0001c0001t0001g0012a0001c0001t0001g0020a0001c0001t0001g0023others(5): Show | 9 | HG01243.hp1 HG01884.hp2 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.147+16672T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76005649 | ||||||
chr14:76005742
|
T | G | 8 | a0001c0001t0001g0012a0001c0001t0001g0020a0001c0001t0001g0023others(5): Show | 9 | HG01243.hp1 HG01884.hp2 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.148-16585T>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76005742 | ||||||
chr14:76005931
|
C | A | 1 | a0001c0001t0001g0143 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.148-16396C>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76005931 | ||||||
chr14:76006061
|
G | A | 1 | a0001c0001t0001g0223 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.148-16266G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76006061 | ||||||
chr14:76006216
|
C | T | 7 | a0001c0001t0001g0009a0001c0001t0001g0105a0001c0001t0001g0251others(4): Show | 8 | HG01891.hp2 HG02615.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.148-16111C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76006216 | ||||||
chr14:76006225
|
G | A | 1 | a0001c0001t0001g0016 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.148-16102G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76006225 | ||||||
chr14:76006423
|
T | C | 8 | a0001c0001t0001g0012a0001c0001t0001g0020a0001c0001t0001g0023others(5): Show | 9 | HG01243.hp1 HG01884.hp2 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.148-15904T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76006423 | ||||||
chr14:76006615
|
C | T | 6 | a0001c0001t0001g0020a0001c0001t0001g0023a0001c0001t0001g0024others(3): Show | 6 | HG01243.hp1 HG01884.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.148-15712C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76006615 | ||||||
chr14:76006782
|
C | T | 6 | a0001c0001t0001g0020a0001c0001t0001g0023a0001c0001t0001g0024others(3): Show | 6 | HG01243.hp1 HG01884.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.148-15545C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76006782 | ||||||
chr14:76006838
|
T | G | 1 | a0001c0001t0001g0326 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.148-15489T>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76006838 | ||||||
chr14:76006855
|
A | AT | 87 | a0001c0001t0001g0010a0001c0001t0001g0017a0001c0001t0001g0063others(84): Show | 88 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(85): Show |
intron_variant | MODIFIER | c.148-15452dupT | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 76006855 | |||||
chr14:76006855
|
AT | A | 11 | a0001c0001t0001g0012a0001c0001t0001g0020a0001c0001t0001g0023others(8): Show | 12 | HG01243.hp1 HG01884.hp2 HG02895.hp2 others(9): Show |
intron_variant | MODIFIER | c.148-15452delT | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 76006855 | |||||
chr14:76006861
|
T | G | 8 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(5): Show | 8 | HG01109.hp2 HG02486.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.148-15466T>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76006861 | ||||||
chr14:76006930
|
C | T | 8 | a0001c0001t0001g0012a0001c0001t0001g0020a0001c0001t0001g0023others(5): Show | 9 | HG01243.hp1 HG01884.hp2 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.148-15397C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76006930 | ||||||
chr14:76007034
|
T | C | 3 | a0001c0001t0001g0295a0001c0001t0001g0296a0001c0001t0001g0361 | 3 | HG02071.hp1 NA18940.hp1 NA18946.hp1 |
intron_variant | MODIFIER | c.148-15293T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76007034 | ||||||
chr14:76007048
|
G | A | 6 | a0001c0001t0001g0020a0001c0001t0001g0023a0001c0001t0001g0024others(3): Show | 6 | HG01243.hp1 HG01884.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.148-15279G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76007048 | ||||||
chr14:76007098
|
A | G | 1 | a0001c0001t0001g0225 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.148-15229A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76007098 | ||||||
chr14:76007115
|
T | C | 1 | a0001c0001t0001g0068 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.148-15212T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76007115 | ||||||
chr14:76007164
|
C | A | 4 | a0001c0001t0001g0013a0001c0001t0001g0114a0001c0001t0001g0115others(1): Show | 4 | HG02055.hp1 HG02280.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.148-15163C>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76007164 | ||||||
chr14:76007339
|
G | A | 1 | a0001c0001t0001g0011 | 2 | HG01074.hp2 HG01099.hp2 |
intron_variant | MODIFIER | c.148-14988G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76007339 | ||||||
chr14:76007547
|
G | T | 303 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(300): Show | 311 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(308): Show |
intron_variant | MODIFIER | c.148-14780G>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76007547 | ||||||
chr14:76007606
|
G | A | 8 | a0001c0001t0001g0012a0001c0001t0001g0020a0001c0001t0001g0023others(5): Show | 9 | HG01243.hp1 HG01884.hp2 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.148-14721G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76007606 | ||||||
chr14:76007677
|
C | T | 3 | a0001c0001t0001g0159a0001c0001t0001g0160a0001c0001t0001g0161 | 3 | HG01928.hp1 HG01993.hp1 HG02148.hp1 |
intron_variant | MODIFIER | c.148-14650C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76007677 | ||||||
chr14:76007846
|
G | T | 8 | a0001c0001t0001g0012a0001c0001t0001g0020a0001c0001t0001g0023others(5): Show | 9 | HG01243.hp1 HG01884.hp2 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.148-14481G>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76007846 | ||||||
chr14:76007872
|
G | A | 8 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(5): Show | 8 | HG01109.hp2 HG02486.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.148-14455G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76007872 | ||||||
chr14:76007932
|
C | G | 1 | a0001c0001t0001g0162 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.148-14395C>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76007932 | ||||||
chr14:76008077
|
A | G | 2 | a0001c0001t0001g0012a0001c0001t0001g0373 | 3 | HG03491.hp2 HG03492.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.148-14250A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76008077 | ||||||
chr14:76008149
|
T | C | 5 | a0001c0001t0001g0065a0001c0001t0001g0246a0001c0001t0001g0247others(2): Show | 5 | HG02258.hp1 HG02622.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.148-14178T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76008149 | ||||||
chr14:76008425
|
T | G | 8 | a0001c0001t0001g0009a0001c0001t0001g0105a0001c0001t0001g0251others(5): Show | 9 | HG01891.hp2 HG02615.hp2 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.148-13902T>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76008425 | ||||||
chr14:76008740
|
T | C | 1 | a0001c0001t0001g0066 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.148-13587T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76008740 | ||||||
chr14:76009143
|
A | G | 60 | a0001c0001t0001g0004a0001c0001t0001g0021a0001c0001t0001g0022others(57): Show | 61 | HG00099.hp1 HG00408.hp2 HG00597.hp2 others(58): Show |
intron_variant | MODIFIER | c.148-13184A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76009143 | ||||||
chr14:76009169
|
C | T | 3 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0230 | 3 | HG01358.hp2 HG01516.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.148-13158C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76009169 | ||||||
chr14:76009345
|
G | C | 8 | a0001c0001t0001g0074a0001c0001t0001g0092a0001c0001t0001g0093others(5): Show | 8 | HG02109.hp2 HG02572.hp1 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.148-12982G>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76009345 | ||||||
chr14:76009391
|
A | G | 1 | a0001c0001t0001g0065 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.148-12936A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76009391 | ||||||
chr14:76009441
|
CT | C | 6 | a0001c0001t0001g0020a0001c0001t0001g0023a0001c0001t0001g0024others(3): Show | 6 | HG01243.hp1 HG01884.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.148-12885delT | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76009441 | ||||||
chr14:76009485
|
G | A | 1 | a0001c0001t0001g0342 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.148-12842G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76009485 | ||||||
chr14:76009606
|
A | G | 4 | a0001c0001t0001g0065a0001c0001t0001g0246a0001c0001t0001g0247others(1): Show | 4 | HG02258.hp1 HG02622.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.148-12721A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76009606 | ||||||
chr14:76009683
|
G | T | 8 | a0001c0001t0001g0012a0001c0001t0001g0020a0001c0001t0001g0023others(5): Show | 9 | HG01243.hp1 HG01884.hp2 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.148-12644G>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76009683 | ||||||
chr14:76009768
|
C | G | 8 | a0001c0001t0001g0012a0001c0001t0001g0020a0001c0001t0001g0023others(5): Show | 9 | HG01243.hp1 HG01884.hp2 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.148-12559C>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76009768 | ||||||
chr14:76009801
|
G | GTTTTTTT others(3): Show |
8 | a0001c0001t0001g0012a0001c0001t0001g0020a0001c0001t0001g0023others(5): Show | 9 | HG01243.hp1 HG01884.hp2 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.148-12524_148-1251 others(14): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 76009801 | |||||
chr14:76009801
|
GT | G | 7 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0368others(4): Show | 7 | HG01109.hp2 HG02486.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.148-12515delT | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 76009801 | |||||
chr14:76009866
|
C | T | 2 | a0001c0001t0001g0012a0001c0001t0001g0373 | 3 | HG03491.hp2 HG03492.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.148-12461C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76009866 | ||||||
chr14:76009904
|
C | T | 1 | a0001c0001t0001g0280 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.148-12423C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76009904 | ||||||
chr14:76009953
|
C | A | 1 | a0001c0001t0001g0182 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.148-12374C>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76009953 | ||||||
chr14:76009978
|
A | G | 8 | a0001c0001t0001g0009a0001c0001t0001g0105a0001c0001t0001g0251others(5): Show | 9 | HG01891.hp2 HG02615.hp2 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.148-12349A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76009978 | ||||||
chr14:76009991
|
C | T | 165 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(162): Show | 169 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(166): Show |
intron_variant | MODIFIER | c.148-12336C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76009991 | ||||||
chr14:76010114
|
T | C | 1 | a0001c0001t0001g0012 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.148-12213T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76010114 | ||||||
chr14:76010340
|
A | G | 55 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0015others(52): Show | 56 | HG01074.hp1 HG01081.hp1 HG01109.hp2 others(53): Show |
intron_variant | MODIFIER | c.148-11987A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76010340 | ||||||
chr14:76010387
|
C | G | 152 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(149): Show | 162 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(159): Show |
intron_variant | MODIFIER | c.148-11940C>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76010387 | ||||||
chr14:76010468
|
A | G | 3 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0380 | 3 | HG02055.hp1 HG02280.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.148-11859A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76010468 | ||||||
chr14:76010498
|
G | A | 33 | a0001c0001t0001g0013a0001c0001t0001g0016a0001c0001t0001g0023others(30): Show | 33 | HG01167.hp1 HG01243.hp1 HG01433.hp1 others(30): Show |
intron_variant | MODIFIER | c.148-11829G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76010498 | ||||||
chr14:76010524
|
A | G | 1 | a0001c0001t0001g0016 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.148-11803A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76010524 | ||||||
chr14:76010643
|
G | A | 3 | a0001c0001t0001g0013a0001c0001t0001g0227a0001c0001t0001g0256 | 3 | HG01167.hp1 HG02965.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.148-11684G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76010643 | ||||||
chr14:76010679
|
T | G | 2 | a0001c0001t0001g0034a0001c0001t0001g0132 | 2 | NA19240.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.148-11648T>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76010679 | ||||||
chr14:76010803
|
G | T | 11 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0023others(8): Show | 11 | HG01167.hp1 HG01243.hp1 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.148-11524G>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76010803 | ||||||
chr14:76010902
|
T | TA | 20 | a0001c0001t0001g0009a0001c0001t0001g0061a0001c0001t0001g0087others(17): Show | 21 | HG01891.hp2 HG01934.hp2 HG02027.hp1 others(18): Show |
intron_variant | MODIFIER | c.148-11425_148-1142 others(5): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76010902 | ||||||
chr14:76010903
|
C | A | 276 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(273): Show | 282 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(279): Show |
intron_variant | MODIFIER | c.148-11424C>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76010903 | ||||||
chr14:76010904
|
C | T | 20 | a0001c0001t0001g0009a0001c0001t0001g0061a0001c0001t0001g0087others(17): Show | 21 | HG01891.hp2 HG01934.hp2 HG02027.hp1 others(18): Show |
intron_variant | MODIFIER | c.148-11423C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76010904 | ||||||
chr14:76010904
|
CT | C | 10 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0128others(7): Show | 10 | HG02055.hp1 HG02280.hp2 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.148-11408delT | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 76010904 | |||||
chr14:76010953
|
A | T | 1 | a0001c0001t0001g0135 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.148-11374A>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76010953 | ||||||
chr14:76010995
|
T | C | 1 | a0001c0001t0001g0342 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.148-11332T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76010995 | ||||||
chr14:76011068
|
AATTATT | A | 3 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0119 | 3 | HG02486.hp1 HG02723.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.148-11243_148-1123 others(10): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 76011068 | |||||
chr14:76011102
|
G | T | 7 | a0001c0001t0001g0020a0001c0001t0001g0023a0001c0001t0001g0024others(4): Show | 7 | HG01243.hp1 HG01884.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.148-11225G>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76011102 | ||||||
chr14:76011183
|
T | C | 56 | a0001c0001t0001g0004a0001c0001t0001g0021a0001c0001t0001g0022others(53): Show | 57 | HG00099.hp1 HG00408.hp2 HG00597.hp2 others(54): Show |
intron_variant | MODIFIER | c.148-11144T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76011183 | ||||||
chr14:76011360
|
A | G | 7 | a0001c0001t0001g0020a0001c0001t0001g0023a0001c0001t0001g0024others(4): Show | 7 | HG01243.hp1 HG01884.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.148-10967A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76011360 | ||||||
chr14:76011425
|
T | A | 1 | a0001c0001t0001g0016 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.148-10902T>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76011425 | ||||||
chr14:76011442
|
C | A | 7 | a0001c0001t0001g0020a0001c0001t0001g0023a0001c0001t0001g0024others(4): Show | 7 | HG01243.hp1 HG01884.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.148-10885C>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76011442 | ||||||
chr14:76011769
|
T | C | 3 | a0001c0001t0001g0024a0001c0001t0001g0058a0001c0001t0001g0060 | 3 | HG02895.hp2 HG02965.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.148-10558T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76011769 | ||||||
chr14:76011770
|
A | G | 1 | a0001c0001t0001g0373 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.148-10557A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76011770 | ||||||
chr14:76011786
|
G | T | 5 | a0001c0001t0001g0320a0001c0001t0001g0321a0001c0001t0001g0322others(2): Show | 5 | HG00735.hp1 HG01981.hp1 HG02148.hp2 others(2): Show |
intron_variant | MODIFIER | c.148-10541G>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76011786 | ||||||
chr14:76011890
|
C | T | 7 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0368others(4): Show | 7 | HG01109.hp2 HG02486.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.148-10437C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76011890 | ||||||
chr14:76011921
|
C | A | 1 | a0001c0001t0001g0199 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.148-10406C>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76011921 | ||||||
chr14:76012018
|
G | C | 7 | a0001c0001t0001g0020a0001c0001t0001g0023a0001c0001t0001g0024others(4): Show | 7 | HG01243.hp1 HG01884.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.148-10309G>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76012018 | ||||||
chr14:76012024
|
T | C | 1 | a0001c0001t0001g0134 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.148-10303T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76012024 | ||||||
chr14:76012071
|
T | G | 1 | a0001c0001t0001g0066 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.148-10256T>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76012071 | ||||||
chr14:76012148
|
G | T | 1 | a0001c0001t0001g0118 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.148-10179G>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76012148 | ||||||
chr14:76012319
|
CCATATAA others(10): Show |
C | 1 | a0001c0001t0001g0022 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.148-10005_148-9989 others(20): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 76012319 | |||||
chr14:76012382
|
T | C | 3 | a0001c0001t0001g0108a0001c0001t0001g0109a0001c0001t0001g0289 | 3 | HG01516.hp2 HG01517.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.148-9945T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76012382 | ||||||
chr14:76012497
|
G | A | 7 | a0001c0001t0001g0020a0001c0001t0001g0023a0001c0001t0001g0024others(4): Show | 7 | HG01243.hp1 HG01884.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.148-9830G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76012497 | ||||||
chr14:76012586
|
G | A | 1 | a0001c0001t0001g0309 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.148-9741G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76012586 | ||||||
chr14:76012671
|
A | G | 1 | a0001c0001t0001g0054 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.148-9656A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76012671 | ||||||
chr14:76012713
|
A | G | 1 | a0001c0001t0001g0066 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.148-9614A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76012713 | ||||||
chr14:76012763
|
CTCTT | C | 6 | a0001c0001t0001g0020a0001c0001t0001g0023a0001c0001t0001g0024others(3): Show | 6 | HG01243.hp1 HG01884.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.148-9558_148-9555d others(6): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 76012763 | |||||
chr14:76013018
|
G | A | 7 | a0001c0001t0001g0020a0001c0001t0001g0023a0001c0001t0001g0024others(4): Show | 7 | HG01243.hp1 HG01884.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.148-9309G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76013018 | ||||||
chr14:76013237
|
A | C | 55 | a0001c0001t0001g0004a0001c0001t0001g0021a0001c0001t0001g0022others(52): Show | 56 | HG00099.hp1 HG00408.hp2 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.148-9090A>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76013237 | ||||||
chr14:76013398
|
A | C | 7 | a0001c0001t0001g0020a0001c0001t0001g0023a0001c0001t0001g0024others(4): Show | 7 | HG01243.hp1 HG01884.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.148-8929A>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76013398 | ||||||
chr14:76013410
|
G | A | 1 | a0001c0001t0001g0368 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.148-8917G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76013410 | ||||||
chr14:76013415
|
C | T | 3 | a0001c0001t0001g0013a0001c0001t0001g0066a0001c0001t0001g0256 | 3 | HG02965.hp2 NA19043.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.148-8912C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76013415 | ||||||
chr14:76013418
|
C | T | 7 | a0001c0001t0001g0020a0001c0001t0001g0023a0001c0001t0001g0024others(4): Show | 7 | HG01243.hp1 HG01884.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.148-8909C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76013418 | ||||||
chr14:76013419
|
G | A | 1 | a0001c0001t0001g0069 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.148-8908G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76013419 | ||||||
chr14:76013435
|
C | T | 5 | a0001c0001t0001g0061a0001c0001t0001g0080a0001c0001t0001g0081others(2): Show | 5 | HG02451.hp1 HG02647.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.148-8892C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76013435 | ||||||
chr14:76013518
|
A | G | 1 | a0001c0001t0001g0304 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.148-8809A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76013518 | ||||||
chr14:76013537
|
C | T | 8 | a0001c0001t0001g0009a0001c0001t0001g0105a0001c0001t0001g0251others(5): Show | 9 | HG01891.hp2 HG02615.hp2 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.148-8790C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76013537 | ||||||
chr14:76013583
|
G | A | 6 | a0001c0001t0001g0020a0001c0001t0001g0023a0001c0001t0001g0024others(3): Show | 6 | HG01243.hp1 HG01884.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.148-8744G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76013583 | ||||||
chr14:76013885
|
TAAAACAA others(3): Show |
T | 6 | a0001c0001t0001g0020a0001c0001t0001g0023a0001c0001t0001g0024others(3): Show | 6 | HG01243.hp1 HG01884.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.148-8438_148-8429d others(12): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 76013885 | |||||
chr14:76014045
|
G | A | 1 | a0001c0001t0001g0134 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.148-8282G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76014045 | ||||||
chr14:76014102
|
A | G | 1 | a0001c0001t0001g0066 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.148-8225A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76014102 | ||||||
chr14:76014232
|
A | G | 1 | a0001c0001t0001g0281 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.148-8095A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76014232 | ||||||
chr14:76014341
|
C | G | 9 | a0001c0001t0001g0074a0001c0001t0001g0092a0001c0001t0001g0093others(6): Show | 9 | HG02109.hp2 HG02572.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.148-7986C>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76014341 | ||||||
chr14:76014651
|
A | AG | 7 | a0001c0001t0001g0020a0001c0001t0001g0023a0001c0001t0001g0024others(4): Show | 7 | HG01243.hp1 HG01884.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.148-7676_148-7675i others(3): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76014651 | ||||||
chr14:76014720
|
T | C | 26 | a0001c0001t0001g0201a0001c0001t0001g0202a0001c0001t0001g0203others(23): Show | 26 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(23): Show |
intron_variant | MODIFIER | c.148-7607T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76014720 | ||||||
chr14:76014728
|
G | A | 2 | a0001c0001t0001g0273a0001c0001t0001g0274 | 2 | NA18980.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.148-7599G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76014728 | ||||||
chr14:76014814
|
G | C | 290 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(287): Show | 297 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(294): Show |
intron_variant | MODIFIER | c.148-7513G>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76014814 | ||||||
chr14:76014840
|
G | C | 1 | a0001c0001t0001g0013 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.148-7487G>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76014840 | ||||||
chr14:76014880
|
A | G | 1 | a0001c0001t0001g0090 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.148-7447A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76014880 | ||||||
chr14:76014941
|
G | T | 1 | a0001c0001t0001g0115 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.148-7386G>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76014941 | ||||||
chr14:76015014
|
A | G | 1 | a0001c0001t0001g0284 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.148-7313A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76015014 | ||||||
chr14:76015042
|
T | A | 1 | a0001c0001t0001g0227 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.148-7285T>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76015042 | ||||||
chr14:76015062
|
C | G | 9 | a0001c0001t0001g0074a0001c0001t0001g0092a0001c0001t0001g0093others(6): Show | 9 | HG02109.hp2 HG02572.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.148-7265C>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76015062 | ||||||
chr14:76015146
|
TATTA | T | 8 | a0001c0001t0001g0009a0001c0001t0001g0105a0001c0001t0001g0251others(5): Show | 9 | HG01891.hp2 HG02615.hp2 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.148-7175_148-7172d others(6): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 76015146 | |||||
chr14:76015299
|
C | G | 3 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0380 | 3 | HG02055.hp1 HG02280.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.148-7028C>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76015299 | ||||||
chr14:76015361
|
C | T | 8 | a0001c0001t0001g0074a0001c0001t0001g0092a0001c0001t0001g0093others(5): Show | 8 | HG02109.hp2 HG02572.hp1 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.148-6966C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76015361 | ||||||
chr14:76015599
|
A | T | 39 | a0001c0001t0001g0003a0001c0001t0001g0025a0001c0001t0001g0026others(36): Show | 40 | HG01074.hp1 HG01081.hp1 HG01175.hp1 others(37): Show |
intron_variant | MODIFIER | c.148-6728A>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76015599 | ||||||
chr14:76015804
|
T | C | 7 | a0001c0001t0001g0020a0001c0001t0001g0023a0001c0001t0001g0024others(4): Show | 7 | HG01243.hp1 HG01884.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.148-6523T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76015804 | ||||||
chr14:76015825
|
C | T | 55 | a0001c0001t0001g0004a0001c0001t0001g0021a0001c0001t0001g0022others(52): Show | 56 | HG00099.hp1 HG00408.hp2 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.148-6502C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76015825 | ||||||
chr14:76015826
|
G | A | 6 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0121others(3): Show | 6 | HG00609.hp2 NA18964.hp1 NA18967.hp1 others(3): Show |
intron_variant | MODIFIER | c.148-6501G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76015826 | ||||||
chr14:76015845
|
A | G | 1 | a0001c0001t0001g0016 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.148-6482A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76015845 | ||||||
chr14:76015963
|
G | A | 1 | a0001c0001t0001g0324 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.148-6364G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76015963 | ||||||
chr14:76016035
|
A | G | 26 | a0001c0001t0001g0201a0001c0001t0001g0202a0001c0001t0001g0203others(23): Show | 26 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(23): Show |
intron_variant | MODIFIER | c.148-6292A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76016035 | ||||||
chr14:76016102
|
A | G | 1 | a0001c0001t0001g0256 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.148-6225A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76016102 | ||||||
chr14:76016256
|
G | T | 1 | a0001c0001t0001g0373 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.148-6071G>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76016256 | ||||||
chr14:76016269
|
G | T | 3 | a0001c0001t0001g0295a0001c0001t0001g0296a0001c0001t0001g0361 | 3 | HG02071.hp1 NA18940.hp1 NA18946.hp1 |
intron_variant | MODIFIER | c.148-6058G>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76016269 | ||||||
chr14:76016273
|
A | G | 55 | a0001c0001t0001g0004a0001c0001t0001g0021a0001c0001t0001g0022others(52): Show | 56 | HG00099.hp1 HG00408.hp2 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.148-6054A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76016273 | ||||||
chr14:76016277
|
A | G | 6 | a0001c0001t0001g0065a0001c0001t0001g0066a0001c0001t0001g0246others(3): Show | 6 | HG02258.hp1 HG02622.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.148-6050A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76016277 | ||||||
chr14:76016341
|
T | G | 1 | a0001c0001t0001g0285 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.148-5986T>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76016341 | ||||||
chr14:76016347
|
C | A | 3 | a0001c0001t0001g0246a0001c0001t0001g0247a0001c0001t0001g0248 | 3 | HG02258.hp1 HG02647.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.148-5980C>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76016347 | ||||||
chr14:76016385
|
T | C | 1 | a0001c0001t0001g0042 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.148-5942T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76016385 | ||||||
chr14:76016519
|
A | G | 8 | a0001c0001t0001g0009a0001c0001t0001g0105a0001c0001t0001g0251others(5): Show | 9 | HG01891.hp2 HG02615.hp2 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.148-5808A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76016519 | ||||||
chr14:76016599
|
G | A | 1 | a0001c0001t0001g0373 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.148-5728G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76016599 | ||||||
chr14:76016694
|
A | T | 1 | a0001c0001t0001g0135 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.148-5633A>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76016694 | ||||||
chr14:76017094
|
G | T | 1 | a0001c0001t0001g0257 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.148-5233G>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76017094 | ||||||
chr14:76017100
|
G | C | 1 | a0001c0001t0001g0257 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.148-5227G>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76017100 | ||||||
chr14:76017163
|
C | T | 1 | a0001c0001t0001g0013 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.148-5164C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76017163 | ||||||
chr14:76017240
|
T | C | 1 | a0001c0001t0001g0094 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.148-5087T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76017240 | ||||||
chr14:76017299
|
A | G | 7 | a0001c0001t0001g0020a0001c0001t0001g0023a0001c0001t0001g0024others(4): Show | 7 | HG01243.hp1 HG01884.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.148-5028A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76017299 | ||||||
chr14:76017460
|
G | C | 9 | a0001c0001t0001g0074a0001c0001t0001g0092a0001c0001t0001g0093others(6): Show | 9 | HG02109.hp2 HG02572.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.148-4867G>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76017460 | ||||||
chr14:76017693
|
G | T | 7 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0368others(4): Show | 7 | HG01109.hp2 HG02486.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.148-4634G>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76017693 | ||||||
chr14:76017746
|
C | G | 55 | a0001c0001t0001g0004a0001c0001t0001g0021a0001c0001t0001g0022others(52): Show | 56 | HG00099.hp1 HG00408.hp2 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.148-4581C>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76017746 | ||||||
chr14:76017756
|
A | G | 1 | a0001c0001t0001g0110 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.148-4571A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76017756 | ||||||
chr14:76017772
|
A | G | 6 | a0001c0001t0001g0035a0001c0001t0001g0037a0001c0001t0001g0038others(3): Show | 6 | NA18960.hp1 NA18963.hp1 NA18991.hp2 others(3): Show |
intron_variant | MODIFIER | c.148-4555A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76017772 | ||||||
chr14:76017837
|
T | C | 4 | a0001c0001t0001g0125a0001c0001t0001g0128a0001c0001t0001g0129others(1): Show | 4 | NA18967.hp2 NA18982.hp2 NA18997.hp2 others(1): Show |
intron_variant | MODIFIER | c.148-4490T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76017837 | ||||||
chr14:76018001
|
C | T | 7 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0046others(4): Show | 7 | HG01175.hp1 HG01928.hp2 HG01943.hp1 others(4): Show |
intron_variant | MODIFIER | c.148-4326C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76018001 | ||||||
chr14:76018090
|
T | G | 1 | a0001c0001t0001g0022 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.148-4237T>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76018090 | ||||||
chr14:76018161
|
C | T | 1 | a0001c0001t0001g0022 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.148-4166C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76018161 | ||||||
chr14:76018163
|
T | C | 1 | a0001c0001t0001g0022 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.148-4164T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76018163 | ||||||
chr14:76018242
|
T | C | 1 | a0001c0001t0001g0227 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.148-4085T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76018242 | ||||||
chr14:76018374
|
T | C | 1 | a0001c0001t0001g0022 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.148-3953T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76018374 | ||||||
chr14:76018378
|
G | A | 1 | a0001c0001t0001g0022 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.148-3949G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76018378 | ||||||
chr14:76018379
|
A | T | 1 | a0001c0001t0001g0022 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.148-3948A>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76018379 | ||||||
chr14:76018381
|
T | G | 3 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0380 | 3 | HG02055.hp1 HG02280.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.148-3946T>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76018381 | ||||||
chr14:76018578
|
G | A | 3 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0230 | 3 | HG01358.hp2 HG01516.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.148-3749G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76018578 | ||||||
chr14:76018849
|
C | G | 94 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(91): Show | 97 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(94): Show |
intron_variant | MODIFIER | c.148-3478C>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76018849 | ||||||
chr14:76018859
|
T | G | 1 | a0001c0001t0001g0363 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.148-3468T>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76018859 | ||||||
chr14:76018952
|
C | A | 9 | a0001c0001t0001g0074a0001c0001t0001g0092a0001c0001t0001g0093others(6): Show | 9 | HG02109.hp2 HG02572.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.148-3375C>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76018952 | ||||||
chr14:76018962
|
T | C | 7 | a0001c0001t0001g0020a0001c0001t0001g0023a0001c0001t0001g0024others(4): Show | 7 | HG01243.hp1 HG01884.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.148-3365T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76018962 | ||||||
chr14:76018968
|
G | A | 7 | a0001c0001t0001g0317a0001c0001t0001g0328a0001c0001t0001g0331others(4): Show | 7 | HG00673.hp2 HG02132.hp1 NA18949.hp2 others(4): Show |
intron_variant | MODIFIER | c.148-3359G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76018968 | ||||||
chr14:76019085
|
A | C | 3 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0380 | 3 | HG02055.hp1 HG02280.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.148-3242A>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76019085 | ||||||
chr14:76019122
|
TTTTCTGA others(4): Show |
T | 1 | a0001c0001t0001g0143 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.148-3204_148-3194d others(13): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76019122 | ||||||
chr14:76019153
|
T | C | 1 | a0001c0001t0001g0073 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.148-3174T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76019153 | ||||||
chr14:76019191
|
A | T | 1 | a0001c0001t0001g0373 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.148-3136A>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76019191 | ||||||
chr14:76019269
|
A | G | 7 | a0001c0001t0001g0020a0001c0001t0001g0023a0001c0001t0001g0024others(4): Show | 7 | HG01243.hp1 HG01884.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.148-3058A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76019269 | ||||||
chr14:76019378
|
C | CT | 15 | a0001c0001t0001g0075a0001c0001t0001g0076a0001c0001t0001g0077others(12): Show | 15 | HG01106.hp1 HG01433.hp1 HG01496.hp1 others(12): Show |
intron_variant | MODIFIER | c.148-2938dupT | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 76019378 | |||||
chr14:76019390
|
C | T | 7 | a0001c0001t0001g0020a0001c0001t0001g0023a0001c0001t0001g0024others(4): Show | 7 | HG01243.hp1 HG01884.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.148-2937C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76019390 | ||||||
chr14:76019533
|
T | C | 1 | a0001c0001t0001g0279 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.148-2794T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76019533 | ||||||
chr14:76019838
|
T | C | 12 | a0001c0001t0001g0003a0001c0001t0001g0028a0001c0001t0001g0029others(9): Show | 13 | HG01074.hp1 HG01081.hp1 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.148-2489T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76019838 | ||||||
chr14:76019887
|
T | G | 1 | a0001c0001t0001g0020 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.148-2440T>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76019887 | ||||||
chr14:76019944
|
A | G | 1 | a0001c0001t0001g0297 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.148-2383A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76019944 | ||||||
chr14:76020002
|
A | C | 1 | a0001c0001t0001g0013 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.148-2325A>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76020002 | ||||||
chr14:76020132
|
G | A | 1 | a0001c0001t0001g0210 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.148-2195G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76020132 | ||||||
chr14:76020155
|
A | G | 1 | a0001c0001t0001g0078 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.148-2172A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76020155 | ||||||
chr14:76020200
|
C | G | 1 | a0001c0001t0001g0020 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.148-2127C>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76020200 | ||||||
chr14:76020364
|
G | T | 7 | a0001c0001t0001g0020a0001c0001t0001g0023a0001c0001t0001g0024others(4): Show | 7 | HG01243.hp1 HG01884.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.148-1963G>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76020364 | ||||||
chr14:76020386
|
C | T | 1 | a0001c0001t0001g0102 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.148-1941C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76020386 | ||||||
chr14:76020397
|
T | C | 8 | a0001c0001t0001g0013a0001c0001t0001g0065a0001c0001t0001g0066others(5): Show | 8 | HG01167.hp1 HG02258.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.148-1930T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76020397 | ||||||
chr14:76020455
|
A | G | 1 | a0001c0001t0001g0066 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.148-1872A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76020455 | ||||||
chr14:76020514
|
A | G | 3 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0380 | 3 | HG02055.hp1 HG02280.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.148-1813A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76020514 | ||||||
chr14:76020543
|
T | C | 39 | a0001c0001t0001g0003a0001c0001t0001g0025a0001c0001t0001g0026others(36): Show | 40 | HG01074.hp1 HG01081.hp1 HG01175.hp1 others(37): Show |
intron_variant | MODIFIER | c.148-1784T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76020543 | ||||||
chr14:76020683
|
G | T | 1 | a0001c0001t0001g0284 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.148-1644G>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76020683 | ||||||
chr14:76020687
|
G | C | 1 | a0001c0001t0001g0227 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.148-1640G>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76020687 | ||||||
chr14:76020863
|
C | T | 7 | a0001c0001t0001g0013a0001c0001t0001g0065a0001c0001t0001g0066others(4): Show | 7 | HG02258.hp1 HG02622.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.148-1464C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76020863 | ||||||
chr14:76020864
|
G | A | 5 | a0001c0001t0001g0368a0001c0001t0001g0369a0001c0001t0001g0370others(2): Show | 5 | HG01109.hp2 HG02486.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.148-1463G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76020864 | ||||||
chr14:76021011
|
C | T | 7 | a0001c0001t0001g0020a0001c0001t0001g0023a0001c0001t0001g0024others(4): Show | 7 | HG01243.hp1 HG01884.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.148-1316C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76021011 | ||||||
chr14:76021141
|
G | A | 1 | a0001c0001t0001g0304 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.148-1186G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76021141 | ||||||
chr14:76021203
|
G | C | 1 | a0001c0001t0001g0257 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.148-1124G>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76021203 | ||||||
chr14:76021309
|
A | G | 1 | a0001c0001t0001g0227 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.148-1018A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76021309 | ||||||
chr14:76021348
|
A | G | 55 | a0001c0001t0001g0004a0001c0001t0001g0021a0001c0001t0001g0022others(52): Show | 56 | HG00099.hp1 HG00408.hp2 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.148-979A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76021348 | ||||||
chr14:76021442
|
A | G | 1 | a0001c0001t0001g0227 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.148-885A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76021442 | ||||||
chr14:76021451
|
A | T | 1 | a0001c0001t0001g0373 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.148-876A>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76021451 | ||||||
chr14:76021478
|
A | G | 8 | a0001c0001t0001g0013a0001c0001t0001g0065a0001c0001t0001g0066others(5): Show | 8 | HG01167.hp1 HG02258.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.148-849A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76021478 | ||||||
chr14:76021571
|
T | C | 1 | a0001c0001t0001g0373 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.148-756T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76021571 | ||||||
chr14:76021923
|
T | G | 7 | a0001c0001t0001g0020a0001c0001t0001g0023a0001c0001t0001g0024others(4): Show | 7 | HG01243.hp1 HG01884.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.148-404T>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76021923 | ||||||
chr14:76022207
|
C | T | 8 | a0001c0001t0001g0074a0001c0001t0001g0092a0001c0001t0001g0093others(5): Show | 8 | HG02109.hp2 HG02572.hp1 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.148-120C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76022207 | ||||||
chr14:76022208
|
A | G | 380 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(377): Show | 395 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(392): Show |
intron_variant | MODIFIER | c.148-119A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76022208 | ||||||
chr14:76022250
|
C | CA | 7 | a0001c0001t0001g0020a0001c0001t0001g0023a0001c0001t0001g0024others(4): Show | 7 | HG01243.hp1 HG01884.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.148-71dupA | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 76022250 | |||||
chr14:76022262
|
A | T | 7 | a0001c0001t0001g0020a0001c0001t0001g0023a0001c0001t0001g0024others(4): Show | 7 | HG01243.hp1 HG01884.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.148-65A>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76022262 | ||||||
chr14:76022507
|
C | A | 1 | a0001c0001t0001g0373 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.215+113C>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76022507 | ||||||
chr14:76022528
|
A | G | 7 | a0001c0001t0001g0020a0001c0001t0001g0023a0001c0001t0001g0024others(4): Show | 7 | HG01243.hp1 HG01884.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.215+134A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76022528 | ||||||
chr14:76022609
|
C | T | 39 | a0001c0001t0001g0003a0001c0001t0001g0025a0001c0001t0001g0026others(36): Show | 40 | HG01074.hp1 HG01081.hp1 HG01175.hp1 others(37): Show |
intron_variant | MODIFIER | c.215+215C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76022609 | ||||||
chr14:76022732
|
A | G | 5 | a0001c0001t0001g0334a0001c0001t0001g0338a0001c0001t0001g0345others(2): Show | 5 | NA18940.hp2 NA18941.hp1 NA18957.hp2 others(2): Show |
intron_variant | MODIFIER | c.215+338A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76022732 | ||||||
chr14:76022741
|
C | G | 377 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(374): Show | 392 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(389): Show |
intron_variant | MODIFIER | c.215+347C>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76022741 | ||||||
chr14:76022790
|
A | G | 1 | a0001c0001t0001g0110 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.215+396A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76022790 | ||||||
chr14:76022929
|
G | A | 1 | a0001c0001t0001g0256 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.215+535G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76022929 | ||||||
chr14:76023006
|
C | G | 2 | a0001c0001t0001g0100a0001c0001t0001g0265 | 2 | HG01891.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.215+612C>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76023006 | ||||||
chr14:76023108
|
T | G | 297 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(294): Show | 304 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(301): Show |
intron_variant | MODIFIER | c.215+714T>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76023108 | ||||||
chr14:76023144
|
T | C | 1 | a0001c0001t0001g0069 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.215+750T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76023144 | ||||||
chr14:76023171
|
A | G | 7 | a0001c0001t0001g0020a0001c0001t0001g0023a0001c0001t0001g0024others(4): Show | 7 | HG01243.hp1 HG01884.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.215+777A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76023171 | ||||||
chr14:76023254
|
A | T | 1 | a0001c0001t0001g0016 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.215+860A>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76023254 | ||||||
chr14:76023534
|
G | T | 1 | a0001c0001t0001g0066 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.215+1140G>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76023534 | ||||||
chr14:76023557
|
T | C | 7 | a0001c0001t0001g0020a0001c0001t0001g0023a0001c0001t0001g0024others(4): Show | 7 | HG01243.hp1 HG01884.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.215+1163T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76023557 | ||||||
chr14:76023735
|
A | C | 5 | a0001c0001t0001g0106a0001c0001t0001g0291a0001c0001t0001g0292others(2): Show | 5 | HG01433.hp1 HG01496.hp1 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.215+1341A>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76023735 | ||||||
chr14:76023735
|
A | G | 1 | a0001c0001t0001g0196 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.215+1341A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76023735 | ||||||
chr14:76023875
|
G | A | 1 | a0001c0001t0001g0227 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.215+1481G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76023875 | ||||||
chr14:76024034
|
C | T | 1 | a0001c0001t0001g0069 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.215+1640C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76024034 | ||||||
chr14:76024192
|
T | C | 295 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(292): Show | 302 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(299): Show |
intron_variant | MODIFIER | c.215+1798T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76024192 | ||||||
chr14:76024393
|
A | G | 7 | a0001c0001t0001g0020a0001c0001t0001g0023a0001c0001t0001g0024others(4): Show | 7 | HG01243.hp1 HG01884.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.215+1999A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76024393 | ||||||
chr14:76024395
|
C | T | 1 | a0001c0001t0001g0232 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.215+2001C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76024395 | ||||||
chr14:76024432
|
A | T | 60 | a0001c0001t0001g0004a0001c0001t0001g0021a0001c0001t0001g0022others(57): Show | 61 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(58): Show |
intron_variant | MODIFIER | c.215+2038A>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76024432 | ||||||
chr14:76024469
|
G | A | 106 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0017others(103): Show | 108 | HG00280.hp2 HG00423.hp2 HG00438.hp2 others(105): Show |
intron_variant | MODIFIER | c.215+2075G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76024469 | ||||||
chr14:76024696
|
G | A | 3 | a0001c0001t0001g0177a0001c0001t0001g0178a0001c0001t0001g0179 | 3 | HG00280.hp1 HG02698.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.215+2302G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76024696 | ||||||
chr14:76024869
|
A | G | 1 | a0001c0001t0001g0295 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.215+2475A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76024869 | ||||||
chr14:76024885
|
T | G | 1 | a0001c0001t0001g0373 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.215+2491T>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76024885 | ||||||
chr14:76025084
|
TA | T | 7 | a0001c0001t0001g0020a0001c0001t0001g0023a0001c0001t0001g0024others(4): Show | 7 | HG01243.hp1 HG01884.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.215+2698delA | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr14 | 76025084 | |||||
chr14:76025091
|
A | T | 3 | a0001c0001t0001g0077a0001c0001t0001g0174a0001c0001t0001g0365 | 3 | HG00642.hp1 HG00735.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.215+2697A>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76025091 | ||||||
chr14:76025108
|
G | T | 3 | a0001c0001t0001g0028a0001c0001t0001g0033a0001c0001t0001g0054 | 3 | HG01074.hp1 HG02886.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.215+2714G>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76025108 | ||||||
chr14:76025224
|
T | A | 7 | a0001c0001t0001g0013a0001c0001t0001g0065a0001c0001t0001g0066others(4): Show | 7 | HG02258.hp1 HG02622.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.215+2830T>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76025224 | ||||||
chr14:76025256
|
A | T | 1 | a0001c0001t0001g0040 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.215+2862A>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76025256 | ||||||
chr14:76025458
|
T | C | 37 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0020others(34): Show | 43 | HG01243.hp1 HG01256.hp2 HG01433.hp1 others(40): Show |
intron_variant | MODIFIER | c.215+3064T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76025458 | ||||||
chr14:76025582
|
C | T | 1 | a0001c0001t0001g0343 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.215+3188C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76025582 | ||||||
chr14:76025611
|
A | G | 111 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0017others(108): Show | 113 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(110): Show |
intron_variant | MODIFIER | c.215+3217A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76025611 | ||||||
chr14:76025849
|
G | A | 1 | a0001c0001t0001g0177 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.215+3455G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76025849 | ||||||
chr14:76025890
|
C | T | 1 | a0001c0001t0001g0206 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.215+3496C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76025890 | ||||||
chr14:76025908
|
G | A | 165 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(162): Show | 170 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(167): Show |
intron_variant | MODIFIER | c.215+3514G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76025908 | ||||||
chr14:76025924
|
G | A | 3 | a0001c0001t0001g0246a0001c0001t0001g0247a0001c0001t0001g0248 | 3 | HG02258.hp1 HG02647.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.215+3530G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76025924 | ||||||
chr14:76025977
|
C | A | 2 | a0001c0001t0001g0066a0001c0001t0001g0256 | 2 | NA19043.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.215+3583C>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76025977 | ||||||
chr14:76026083
|
G | T | 1 | a0001c0001t0001g0373 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.215+3689G>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76026083 | ||||||
chr14:76026123
|
G | A | 1 | a0001c0001t0001g0282 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.215+3729G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76026123 | ||||||
chr14:76026164
|
A | G | 1 | a0001c0001t0001g0373 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.215+3770A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76026164 | ||||||
chr14:76026221
|
A | G | 1 | a0001c0001t0001g0331 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.215+3827A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76026221 | ||||||
chr14:76026276
|
C | T | 7 | a0001c0001t0001g0020a0001c0001t0001g0023a0001c0001t0001g0024others(4): Show | 7 | HG01243.hp1 HG01884.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.215+3882C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76026276 | ||||||
chr14:76026349
|
G | A | 1 | a0001c0001t0001g0294 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.215+3955G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76026349 | ||||||
chr14:76026372
|
G | A | 7 | a0001c0001t0001g0020a0001c0001t0001g0023a0001c0001t0001g0024others(4): Show | 7 | HG01243.hp1 HG01884.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.215+3978G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76026372 | ||||||
chr14:76026552
|
C | CA | 123 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0013others(120): Show | 125 | HG00280.hp2 HG00423.hp2 HG00438.hp2 others(122): Show |
intron_variant | MODIFIER | c.215+4177dupA | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr14 | 76026552 | |||||
chr14:76026552
|
CA | C | 7 | a0001c0001t0001g0009a0001c0001t0001g0105a0001c0001t0001g0251others(4): Show | 8 | HG01891.hp2 HG02615.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.215+4177delA | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr14 | 76026552 | |||||
chr14:76026685
|
A | G | 1 | a0001c0001t0001g0016 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.215+4291A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76026685 | ||||||
chr14:76026876
|
A | G | 1 | a0001c0001t0001g0135 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.215+4482A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76026876 | ||||||
chr14:76026900
|
C | CA | 6 | a0001c0001t0001g0020a0001c0001t0001g0023a0001c0001t0001g0024others(3): Show | 6 | HG01243.hp1 HG01884.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.215+4514dupA | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr14 | 76026900 | |||||
chr14:76027142
|
A | G | 2 | a0001c0001t0001g0013a0001c0001t0001g0114 | 2 | HG02280.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.215+4748A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76027142 | ||||||
chr14:76027252
|
A | G | 9 | a0001c0001t0001g0074a0001c0001t0001g0092a0001c0001t0001g0093others(6): Show | 9 | HG02109.hp2 HG02572.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.215+4858A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76027252 | ||||||
chr14:76027336
|
C | T | 1 | a0001c0001t0001g0227 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.215+4942C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76027336 | ||||||
chr14:76027340
|
A | C | 127 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(124): Show | 130 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(127): Show |
intron_variant | MODIFIER | c.215+4946A>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76027340 | ||||||
chr14:76027348
|
A | T | 2 | a0001c0001t0001g0126a0001c0001t0001g0256 | 2 | HG01069.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.215+4954A>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76027348 | ||||||
chr14:76027349
|
C | CACTT | 292 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(289): Show | 299 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(296): Show |
intron_variant | MODIFIER | c.215+4955_215+4956i others(6): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76027349 | ||||||
chr14:76027349
|
C | T | 2 | a0001c0001t0001g0126a0001c0001t0001g0256 | 2 | HG01069.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.215+4955C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76027349 | ||||||
chr14:76027365
|
A | G | 118 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0010others(115): Show | 121 | HG00280.hp2 HG00423.hp2 HG00438.hp2 others(118): Show |
intron_variant | MODIFIER | c.215+4971A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76027365 | ||||||
chr14:76027378
|
G | A | 1 | a0001c0001t0001g0221 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.215+4984G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76027378 | ||||||
chr14:76027408
|
T | C | 1 | a0001c0001t0001g0036 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.215+5014T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76027408 | ||||||
chr14:76027706
|
C | CA | 23 | a0001c0001t0001g0040a0001c0001t0001g0066a0001c0001t0001g0075others(20): Show | 23 | HG01167.hp1 HG02027.hp2 HG02056.hp2 others(20): Show |
intron_variant | MODIFIER | c.215+5330dupA | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr14 | 76027706 | |||||
chr14:76027706
|
CA | C | 119 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(116): Show | 128 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(125): Show |
intron_variant | MODIFIER | c.215+5330delA | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr14 | 76027706 | |||||
chr14:76027720
|
A | T | 6 | a0001c0001t0001g0020a0001c0001t0001g0023a0001c0001t0001g0024others(3): Show | 6 | HG01243.hp1 HG01884.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.215+5326A>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76027720 | ||||||
chr14:76027891
|
G | A | 1 | a0001c0001t0001g0033 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.215+5497G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76027891 | ||||||
chr14:76027907
|
T | C | 5 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0058others(2): Show | 5 | HG01243.hp1 HG01884.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.215+5513T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76027907 | ||||||
chr14:76027960
|
A | G | 6 | a0001c0001t0001g0020a0001c0001t0001g0023a0001c0001t0001g0024others(3): Show | 6 | HG01243.hp1 HG01884.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.215+5566A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76027960 | ||||||
chr14:76028012
|
C | T | 1 | a0001c0001t0001g0115 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.215+5618C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76028012 | ||||||
chr14:76028233
|
T | TG | 6 | a0001c0001t0001g0122a0001c0001t0001g0180a0001c0001t0001g0188others(3): Show | 6 | HG01255.hp2 HG01934.hp2 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.215+5843dupG | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr14 | 76028233 | |||||
chr14:76028241
|
C | T | 1 | a0001c0001t0001g0373 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.215+5847C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76028241 | ||||||
chr14:76028285
|
G | A | 7 | a0001c0001t0001g0020a0001c0001t0001g0023a0001c0001t0001g0024others(4): Show | 7 | HG01243.hp1 HG01884.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.215+5891G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76028285 | ||||||
chr14:76028403
|
T | C | 9 | a0001c0001t0001g0074a0001c0001t0001g0092a0001c0001t0001g0093others(6): Show | 9 | HG02109.hp2 HG02572.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.215+6009T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76028403 | ||||||
chr14:76028748
|
T | C | 1 | a0001c0001t0001g0197 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.215+6354T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76028748 | ||||||
chr14:76028779
|
G | A | 1 | a0001c0001t0001g0373 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.215+6385G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76028779 | ||||||
chr14:76028894
|
C | G | 3 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0380 | 3 | HG02055.hp1 HG02280.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.215+6500C>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76028894 | ||||||
chr14:76028923
|
C | T | 5 | a0001c0001t0001g0215a0001c0001t0001g0228a0001c0001t0001g0229others(2): Show | 5 | HG01256.hp1 HG01258.hp1 HG01934.hp2 others(2): Show |
intron_variant | MODIFIER | c.215+6529C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76028923 | ||||||
chr14:76028972
|
T | C | 2 | a0001c0001t0001g0273a0001c0001t0001g0274 | 2 | NA18980.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.215+6578T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76028972 | ||||||
chr14:76028978
|
C | A | 1 | a0001c0001t0001g0288 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.215+6584C>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76028978 | ||||||
chr14:76028999
|
G | A | 1 | a0001c0001t0001g0120 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.215+6605G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76028999 | ||||||
chr14:76029055
|
C | G | 7 | a0001c0001t0001g0020a0001c0001t0001g0023a0001c0001t0001g0024others(4): Show | 7 | HG01243.hp1 HG01884.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.215+6661C>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76029055 | ||||||
chr14:76029153
|
T | C | 1 | a0001c0001t0001g0069 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.215+6759T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76029153 | ||||||
chr14:76029203
|
A | G | 1 | a0001c0001t0001g0013 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.215+6809A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76029203 | ||||||
chr14:76029218
|
A | G | 6 | a0001c0001t0001g0065a0001c0001t0001g0066a0001c0001t0001g0246others(3): Show | 6 | HG02258.hp1 HG02622.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.215+6824A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76029218 | ||||||
chr14:76029449
|
A | C | 93 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(90): Show | 96 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.215+7055A>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76029449 | ||||||
chr14:76029562
|
T | C | 1 | a0001c0001t0001g0033 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.215+7168T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76029562 | ||||||
chr14:76029579
|
T | C | 1 | a0001c0001t0001g0288 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.215+7185T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76029579 | ||||||
chr14:76029611
|
T | G | 1 | a0001c0001t0001g0052 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.215+7217T>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76029611 | ||||||
chr14:76029851
|
T | TTTTATTT others(7): Show |
1 | a0001c0001t0001g0288 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.215+7460_215+7461i others(16): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr14 | 76029851 | |||||
chr14:76029851
|
T | TTTTTA | 8 | a0001c0001t0001g0018a0001c0001t0001g0044a0001c0001t0001g0084others(5): Show | 8 | HG00597.hp1 HG01168.hp2 HG01928.hp2 others(5): Show |
intron_variant | MODIFIER | c.215+7501_215+7505d others(7): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr14 | 76029851 | |||||
chr14:76029851
|
T | TTTTTATT others(3): Show |
72 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0036others(69): Show | 72 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(69): Show |
intron_variant | MODIFIER | c.215+7496_215+7505d others(12): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr14 | 76029851 | |||||
chr14:76029851
|
T | TTTTTATT others(8): Show |
86 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0009others(83): Show | 89 | HG00099.hp1 HG00423.hp2 HG00597.hp2 others(86): Show |
intron_variant | MODIFIER | c.215+7491_215+7505d others(17): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr14 | 76029851 | |||||
chr14:76029851
|
T | TTTTTATT others(13): Show |
59 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(56): Show | 62 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(59): Show |
intron_variant | MODIFIER | c.215+7486_215+7505d others(22): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr14 | 76029851 | |||||
chr14:76029851
|
T | TTTTTATT others(18): Show |
6 | a0001c0001t0001g0127a0001c0001t0001g0144a0001c0001t0001g0156others(3): Show | 6 | HG02683.hp2 HG03704.hp2 NA18939.hp1 others(3): Show |
intron_variant | MODIFIER | c.215+7481_215+7505d others(27): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr14 | 76029851 | |||||
chr14:76029851
|
TTTTTA | T | 5 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0305others(2): Show | 5 | HG02055.hp1 HG02602.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.215+7501_215+7505d others(7): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr14 | 76029851 | |||||
chr14:76029851
|
TTTTTATT others(3): Show |
T | 6 | a0001c0001t0001g0014a0001c0001t0001g0368a0001c0001t0001g0369others(3): Show | 6 | HG01109.hp2 HG02486.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.215+7496_215+7505d others(12): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr14 | 76029851 | |||||
chr14:76029868
|
T | TTTATTTT others(79): Show |
4 | a0001c0001t0001g0074a0001c0001t0001g0092a0001c0001t0001g0094others(1): Show | 4 | HG02922.hp2 HG02970.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.215+7505_215+7506i others(88): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr14 | 76029868 | |||||
chr14:76029868
|
T | TTTATTTT others(79): Show |
1 | a0001c0001t0001g0096 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.215+7505_215+7506i others(88): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr14 | 76029868 | |||||
chr14:76029868
|
T | TTTATTTT others(84): Show |
4 | a0001c0001t0001g0093a0001c0001t0001g0095a0001c0001t0001g0098others(1): Show | 4 | HG02109.hp2 HG02572.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.215+7505_215+7506i others(93): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr14 | 76029868 | |||||
chr14:76029871
|
A | ATTTTATT others(14): Show |
1 | a0001c0001t0001g0020 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.215+7490_215+7491i others(23): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr14 | 76029871 | |||||
chr14:76029871
|
A | ATTTTATT others(24): Show |
5 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0058others(2): Show | 5 | HG01243.hp1 HG01884.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.215+7500_215+7501i others(33): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr14 | 76029871 | |||||
chr14:76029871
|
A | ATTTTATT others(39): Show |
1 | a0001c0001t0001g0373 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.215+7505_215+7506i others(48): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr14 | 76029871 | |||||
chr14:76029904
|
C | T | 91 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(88): Show | 94 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(91): Show |
intron_variant | MODIFIER | c.215+7510C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76029904 | ||||||
chr14:76029942
|
T | TG | 116 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0013others(113): Show | 118 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(115): Show |
intron_variant | MODIFIER | c.215+7549dupG | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr14 | 76029942 | |||||
chr14:76029978
|
T | C | 1 | a0001c0001t0001g0367 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.215+7584T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76029978 | ||||||
chr14:76030029
|
C | T | 1 | a0001c0001t0001g0013 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.215+7635C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76030029 | ||||||
chr14:76030107
|
C | T | 1 | a0001c0001t0001g0293 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.215+7713C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76030107 | ||||||
chr14:76030134
|
G | T | 3 | a0001c0001t0001g0108a0001c0001t0001g0109a0001c0001t0001g0289 | 3 | HG01516.hp2 HG01517.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.215+7740G>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76030134 | ||||||
chr14:76030229
|
TCA | T | 44 | a0001c0001t0001g0010a0001c0001t0001g0017a0001c0001t0001g0063others(41): Show | 45 | HG00438.hp2 HG00642.hp2 HG01070.hp1 others(42): Show |
intron_variant | MODIFIER | c.215+7838_215+7839d others(4): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr14 | 76030229 | |||||
chr14:76030234
|
G | GT | 7 | a0001c0001t0001g0020a0001c0001t0001g0023a0001c0001t0001g0024others(4): Show | 7 | HG01243.hp1 HG01884.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.215+7849dupT | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr14 | 76030234 | |||||
chr14:76030361
|
C | T | 2 | a0001c0001t0001g0022a0001c0001t0001g0122 | 2 | NA18967.hp1 NA19075.hp2 |
intron_variant | MODIFIER | c.215+7967C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76030361 | ||||||
chr14:76030377
|
A | G | 3 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0230 | 3 | HG01358.hp2 HG01516.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.215+7983A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76030377 | ||||||
chr14:76030397
|
A | G | 1 | a0001c0001t0001g0012 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.215+8003A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76030397 | ||||||
chr14:76030419
|
A | G | 6 | a0001c0001t0001g0020a0001c0001t0001g0023a0001c0001t0001g0024others(3): Show | 6 | HG01243.hp1 HG01884.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.215+8025A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76030419 | ||||||
chr14:76030446
|
T | G | 1 | a0001c0001t0001g0114 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.215+8052T>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76030446 | ||||||
chr14:76030472
|
G | A | 9 | a0001c0001t0001g0009a0001c0001t0001g0105a0001c0001t0001g0251others(6): Show | 10 | HG01884.hp1 HG01891.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.215+8078G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76030472 | ||||||
chr14:76030477
|
A | G | 1 | a0001c0001t0001g0043 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.215+8083A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76030477 | ||||||
chr14:76030528
|
G | A | 6 | a0001c0001t0001g0020a0001c0001t0001g0023a0001c0001t0001g0024others(3): Show | 6 | HG01243.hp1 HG01884.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.215+8134G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76030528 | ||||||
chr14:76030888
|
G | A | 377 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(374): Show | 392 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(389): Show |
intron_variant | MODIFIER | c.215+8494G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76030888 | ||||||
chr14:76030892
|
T | A | 106 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0017others(103): Show | 108 | HG00280.hp2 HG00423.hp2 HG00438.hp2 others(105): Show |
intron_variant | MODIFIER | c.215+8498T>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76030892 | ||||||
chr14:76030979
|
T | A | 1 | a0001c0001t0001g0089 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.215+8585T>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76030979 | ||||||
chr14:76030980
|
T | A | 1 | a0001c0001t0001g0089 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.215+8586T>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76030980 | ||||||
chr14:76030990
|
A | G | 1 | a0001c0001t0001g0066 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.215+8596A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76030990 | ||||||
chr14:76031020
|
G | GTA | 3 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0380 | 3 | HG02055.hp1 HG02280.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.215+8637_215+8638d others(4): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr14 | 76031020 | |||||
chr14:76031030
|
A | G | 9 | a0001c0001t0001g0074a0001c0001t0001g0092a0001c0001t0001g0093others(6): Show | 9 | HG02109.hp2 HG02572.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.215+8636A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76031030 | ||||||
chr14:76031058
|
T | C | 3 | a0002c0002t0001g0356a0002c0002t0001g0357a0002c0002t0001g0362 | 3 | HG02056.hp2 NA18995.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.215+8664T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76031058 | ||||||
chr14:76031118
|
C | T | 8 | a0001c0001t0001g0013a0001c0001t0001g0065a0001c0001t0001g0066others(5): Show | 8 | HG01167.hp1 HG02258.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.215+8724C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76031118 | ||||||
chr14:76031378
|
C | G | 6 | a0001c0001t0001g0020a0001c0001t0001g0023a0001c0001t0001g0024others(3): Show | 6 | HG01243.hp1 HG01884.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.215+8984C>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76031378 | ||||||
chr14:76031443
|
A | G | 7 | a0001c0001t0001g0020a0001c0001t0001g0023a0001c0001t0001g0024others(4): Show | 7 | HG01243.hp1 HG01884.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.215+9049A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76031443 | ||||||
chr14:76031500
|
G | C | 4 | a0001c0001t0001g0065a0001c0001t0001g0246a0001c0001t0001g0247others(1): Show | 4 | HG02258.hp1 HG02622.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.215+9106G>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76031500 | ||||||
chr14:76031609
|
GAAATAAG others(1): Show |
G | 7 | a0001c0001t0001g0020a0001c0001t0001g0023a0001c0001t0001g0024others(4): Show | 7 | HG01243.hp1 HG01884.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.215+9224_215+9231d others(10): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr14 | 76031609 | |||||
chr14:76031679
|
C | T | 1 | a0001c0001t0001g0166 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.215+9285C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76031679 | ||||||
chr14:76031906
|
A | G | 9 | a0001c0001t0001g0074a0001c0001t0001g0092a0001c0001t0001g0093others(6): Show | 9 | HG02109.hp2 HG02572.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.215+9512A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76031906 | ||||||
chr14:76031917
|
C | T | 9 | a0001c0001t0001g0009a0001c0001t0001g0105a0001c0001t0001g0251others(6): Show | 10 | HG01884.hp1 HG01891.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.215+9523C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76031917 | ||||||
chr14:76032101
|
C | T | 6 | a0001c0001t0001g0020a0001c0001t0001g0023a0001c0001t0001g0024others(3): Show | 6 | HG01243.hp1 HG01884.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.215+9707C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76032101 | ||||||
chr14:76032200
|
C | A | 7 | a0001c0001t0001g0020a0001c0001t0001g0023a0001c0001t0001g0024others(4): Show | 7 | HG01243.hp1 HG01884.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.215+9806C>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76032200 | ||||||
chr14:76032217
|
A | G | 1 | a0001c0001t0001g0227 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.215+9823A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76032217 | ||||||
chr14:76032271
|
C | G | 2 | a0001c0001t0001g0302a0001c0001t0001g0305 | 2 | NA18987.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.215+9877C>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76032271 | ||||||
chr14:76032428
|
A | G | 1 | a0001c0001t0001g0013 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.215+10034A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76032428 | ||||||
chr14:76032492
|
C | T | 1 | a0001c0001t0001g0169 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.215+10098C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76032492 | ||||||
chr14:76032555
|
C | G | 5 | a0001c0001t0001g0216a0001c0001t0001g0217a0001c0001t0001g0218others(2): Show | 5 | HG01168.hp1 HG01358.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.215+10161C>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76032555 | ||||||
chr14:76032664
|
C | T | 1 | a0001c0001t0001g0149 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.215+10270C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76032664 | ||||||
chr14:76032727
|
C | T | 7 | a0001c0001t0001g0065a0001c0001t0001g0066a0001c0001t0001g0148others(4): Show | 7 | HG01167.hp1 HG02258.hp1 HG02300.hp1 others(4): Show |
intron_variant | MODIFIER | c.215+10333C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76032727 | ||||||
chr14:76032757
|
G | GA | 4 | a0001c0001t0001g0300a0001c0001t0001g0377a0001c0001t0001g0378others(1): Show | 4 | NA18950.hp1 NA18961.hp1 NA19056.hp1 others(1): Show |
intron_variant | MODIFIER | c.215+10365dupA | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr14 | 76032757 | |||||
chr14:76032793
|
T | C | 1 | a0001c0001t0001g0016 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.215+10399T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76032793 | ||||||
chr14:76032937
|
G | A | 5 | a0001c0001t0001g0368a0001c0001t0001g0369a0001c0001t0001g0370others(2): Show | 5 | HG01109.hp2 HG02486.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.215+10543G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76032937 | ||||||
chr14:76033032
|
A | G | 2 | a0001c0001t0001g0174a0001c0001t0001g0365 | 2 | HG00642.hp1 HG00735.hp2 |
intron_variant | MODIFIER | c.215+10638A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76033032 | ||||||
chr14:76033109
|
G | A | 1 | a0001c0001t0001g0119 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.215+10715G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76033109 | ||||||
chr14:76033117
|
G | A | 1 | a0001c0001t0001g0189 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.215+10723G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76033117 | ||||||
chr14:76033159
|
C | A | 139 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(136): Show | 142 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(139): Show |
intron_variant | MODIFIER | c.215+10765C>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76033159 | ||||||
chr14:76033348
|
C | T | 1 | a0001c0001t0001g0281 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.215+10954C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76033348 | ||||||
chr14:76033411
|
C | T | 84 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(81): Show | 87 | HG00423.hp1 HG00438.hp1 HG00609.hp1 others(84): Show |
intron_variant | MODIFIER | c.215+11017C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76033411 | ||||||
chr14:76033836
|
G | A | 2 | a0001c0001t0001g0026a0001c0001t0001g0027 | 2 | HG02559.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.215+11442G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76033836 | ||||||
chr14:76033930
|
A | G | 9 | a0001c0001t0001g0074a0001c0001t0001g0092a0001c0001t0001g0093others(6): Show | 9 | HG02109.hp2 HG02572.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.215+11536A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76033930 | ||||||
chr14:76033960
|
T | C | 177 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0009others(174): Show | 181 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(178): Show |
intron_variant | MODIFIER | c.215+11566T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76033960 | ||||||
chr14:76033978
|
T | A | 13 | a0001c0001t0001g0005a0001c0001t0001g0046a0001c0001t0001g0141others(10): Show | 14 | HG01070.hp2 HG01106.hp2 HG01175.hp1 others(11): Show |
intron_variant | MODIFIER | c.215+11584T>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76033978 | ||||||
chr14:76034145
|
G | A | 9 | a0001c0001t0001g0009a0001c0001t0001g0105a0001c0001t0001g0251others(6): Show | 10 | HG01884.hp1 HG01891.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.215+11751G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76034145 | ||||||
chr14:76034306
|
G | A | 3 | a0001c0001t0001g0219a0001c0001t0001g0223a0001c0001t0001g0224 | 3 | HG00423.hp2 HG02129.hp1 NA18952.hp1 |
intron_variant | MODIFIER | c.215+11912G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76034306 | ||||||
chr14:76034359
|
T | G | 1 | a0001c0001t0001g0167 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.215+11965T>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76034359 | ||||||
chr14:76034461
|
A | T | 1 | a0001c0001t0001g0066 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.215+12067A>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76034461 | ||||||
chr14:76034478
|
G | A | 1 | a0001c0001t0001g0166 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.215+12084G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76034478 | ||||||
chr14:76034612
|
T | C | 1 | a0001c0001t0001g0126 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.215+12218T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76034612 | ||||||
chr14:76034755
|
T | C | 296 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(293): Show | 303 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(300): Show |
intron_variant | MODIFIER | c.215+12361T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76034755 | ||||||
chr14:76034850
|
G | A | 1 | a0001c0001t0001g0116 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.215+12456G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76034850 | ||||||
chr14:76034957
|
T | G | 1 | a0001c0001t0001g0203 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.215+12563T>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76034957 | ||||||
chr14:76035238
|
A | G | 1 | a0001c0001t0001g0373 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.215+12844A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76035238 | ||||||
chr14:76035677
|
G | A | 6 | a0001c0001t0001g0020a0001c0001t0001g0023a0001c0001t0001g0024others(3): Show | 6 | HG01243.hp1 HG01884.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.215+13283G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76035677 | ||||||
chr14:76035724
|
A | G | 1 | a0001c0001t0001g0373 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.215+13330A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76035724 | ||||||
chr14:76035813
|
A | T | 7 | a0001c0001t0001g0020a0001c0001t0001g0023a0001c0001t0001g0024others(4): Show | 7 | HG01243.hp1 HG01884.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.215+13419A>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76035813 | ||||||
chr14:76035866
|
C | T | 6 | a0001c0001t0001g0020a0001c0001t0001g0023a0001c0001t0001g0024others(3): Show | 6 | HG01243.hp1 HG01884.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.215+13472C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76035866 | ||||||
chr14:76035962
|
G | A | 1 | a0001c0001t0001g0170 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.215+13568G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76035962 | ||||||
chr14:76036111
|
G | T | 1 | a0001c0001t0001g0015 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.215+13717G>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76036111 | ||||||
chr14:76036160
|
C | T | 3 | a0001c0001t0001g0246a0001c0001t0001g0247a0001c0001t0001g0248 | 3 | HG02258.hp1 HG02647.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.215+13766C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76036160 | ||||||
chr14:76036171
|
T | C | 1 | a0001c0001t0001g0373 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.215+13777T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76036171 | ||||||
chr14:76036312
|
T | TTTCC | 6 | a0001c0001t0001g0065a0001c0001t0001g0066a0001c0001t0001g0246others(3): Show | 6 | HG02258.hp1 HG02622.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.215+13938_215+1394 others(8): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr14 | 76036312 | |||||
chr14:76036364
|
T | C | 1 | a0001c0001t0001g0282 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.215+13970T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76036364 | ||||||
chr14:76036369
|
G | A | 15 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0101others(12): Show | 21 | HG01256.hp2 HG01943.hp2 HG01952.hp1 others(18): Show |
intron_variant | MODIFIER | c.215+13975G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76036369 | ||||||
chr14:76036408
|
C | CT | 123 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0017others(120): Show | 125 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(122): Show |
intron_variant | MODIFIER | c.215+14031dupT | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr14 | 76036408 | |||||
chr14:76036553
|
C | T | 46 | a0001c0001t0001g0010a0001c0001t0001g0017a0001c0001t0001g0063others(43): Show | 47 | HG00438.hp2 HG00642.hp2 HG01070.hp1 others(44): Show |
intron_variant | MODIFIER | c.215+14159C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76036553 | ||||||
chr14:76036554
|
G | A | 2 | a0001c0001t0001g0023a0001c0001t0001g0059 | 2 | HG01243.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.215+14160G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76036554 | ||||||
chr14:76036657
|
G | A | 1 | a0001c0001t0001g0163 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.215+14263G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76036657 | ||||||
chr14:76036780
|
A | G | 1 | a0001c0001t0001g0227 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.215+14386A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76036780 | ||||||
chr14:76036790
|
C | T | 1 | a0001c0001t0001g0177 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.215+14396C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76036790 | ||||||
chr14:76036844
|
T | C | 1 | a0001c0001t0001g0016 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.215+14450T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76036844 | ||||||
chr14:76037118
|
A | G | 5 | a0001c0001t0001g0065a0001c0001t0001g0227a0001c0001t0001g0246others(2): Show | 5 | HG01167.hp1 HG02258.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.215+14724A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76037118 | ||||||
chr14:76037176
|
G | GGTGTA | 107 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0017others(104): Show | 109 | HG00280.hp2 HG00423.hp2 HG00438.hp2 others(106): Show |
intron_variant | MODIFIER | c.215+14784_215+1478 others(9): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr14 | 76037176 | |||||
chr14:76037198
|
C | A | 1 | a0001c0001t0001g0103 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.215+14804C>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76037198 | ||||||
chr14:76037356
|
C | T | 1 | a0001c0001t0001g0373 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.215+14962C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76037356 | ||||||
chr14:76037539
|
A | G | 60 | a0001c0001t0001g0004a0001c0001t0001g0021a0001c0001t0001g0022others(57): Show | 61 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(58): Show |
intron_variant | MODIFIER | c.215+15145A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76037539 | ||||||
chr14:76037613
|
G | A | 7 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0368others(4): Show | 7 | HG01109.hp2 HG02486.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.215+15219G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76037613 | ||||||
chr14:76037689
|
C | G | 9 | a0001c0001t0001g0009a0001c0001t0001g0105a0001c0001t0001g0251others(6): Show | 10 | HG01884.hp1 HG01891.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.215+15295C>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76037689 | ||||||
chr14:76037691
|
G | GT | 56 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(53): Show | 63 | HG00099.hp1 HG00733.hp1 HG00735.hp1 others(60): Show |
intron_variant | MODIFIER | c.215+15310dupT | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr14 | 76037691 | |||||
chr14:76037691
|
G | GTT | 254 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(251): Show | 259 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(256): Show |
intron_variant | MODIFIER | c.215+15309_215+1531 others(6): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr14 | 76037691 | |||||
chr14:76037691
|
G | T | 9 | a0001c0001t0001g0009a0001c0001t0001g0105a0001c0001t0001g0251others(6): Show | 10 | HG01884.hp1 HG01891.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.215+15297G>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76037691 | ||||||
chr14:76037693
|
T | TG | 6 | a0001c0001t0001g0020a0001c0001t0001g0023a0001c0001t0001g0024others(3): Show | 6 | HG01243.hp1 HG01884.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.215+15299_215+1530 others(5): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76037693 | ||||||
chr14:76037736
|
G | T | 1 | a0001c0001t0001g0107 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.215+15342G>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76037736 | ||||||
chr14:76037739
|
T | C | 1 | a0001c0001t0001g0112 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.215+15345T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76037739 | ||||||
chr14:76037930
|
A | G | 1 | a0001c0001t0001g0373 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.215+15536A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76037930 | ||||||
chr14:76037988
|
T | C | 1 | a0001c0001t0001g0300 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.215+15594T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76037988 | ||||||
chr14:76038072
|
C | A | 65 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0021others(62): Show | 67 | HG00099.hp1 HG00408.hp2 HG00597.hp2 others(64): Show |
intron_variant | MODIFIER | c.215+15678C>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76038072 | ||||||
chr14:76038081
|
G | A | 3 | a0001c0001t0001g0246a0001c0001t0001g0247a0001c0001t0001g0248 | 3 | HG02258.hp1 HG02647.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.215+15687G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76038081 | ||||||
chr14:76038246
|
C | T | 1 | a0001c0001t0001g0373 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.215+15852C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76038246 | ||||||
chr14:76038303
|
T | C | 1 | a0001c0001t0001g0251 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.215+15909T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76038303 | ||||||
chr14:76038354
|
G | A | 1 | a0001c0001t0001g0013 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.215+15960G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76038354 | ||||||
chr14:76038357
|
A | G | 1 | a0001c0001t0001g0166 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.215+15963A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76038357 | ||||||
chr14:76038455
|
T | C | 1 | a0001c0001t0001g0140 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.215+16061T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76038455 | ||||||
chr14:76038636
|
TA | T | 5 | a0001c0001t0001g0201a0001c0001t0001g0202a0001c0001t0001g0203others(2): Show | 5 | NA18953.hp2 NA18969.hp1 NA18994.hp1 others(2): Show |
intron_variant | MODIFIER | c.215+16243delA | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76038636 | ||||||
chr14:76038642
|
A | G | 3 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0380 | 3 | HG02055.hp1 HG02280.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.215+16248A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76038642 | ||||||
chr14:76038783
|
T | C | 1 | a0001c0001t0001g0101 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.215+16389T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76038783 | ||||||
chr14:76038924
|
T | G | 1 | a0001c0001t0001g0087 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.215+16530T>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76038924 | ||||||
chr14:76038970
|
T | C | 296 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(293): Show | 303 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(300): Show |
intron_variant | MODIFIER | c.215+16576T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76038970 | ||||||
chr14:76039015
|
AC | A | 3 | a0001c0001t0001g0220a0001c0001t0001g0225a0001c0001t0001g0233 | 3 | HG02165.hp1 NA18978.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.215+16622delC | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76039015 | ||||||
chr14:76039130
|
A | AT | 15 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0107others(12): Show | 15 | HG00408.hp2 HG00673.hp1 HG01361.hp2 others(12): Show |
intron_variant | MODIFIER | c.215+16749dupT | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr14 | 76039130 | |||||
chr14:76039130
|
AT | A | 37 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0066others(34): Show | 43 | HG01256.hp2 HG01433.hp1 HG01496.hp1 others(40): Show |
intron_variant | MODIFIER | c.215+16749delT | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr14 | 76039130 | |||||
chr14:76039191
|
G | T | 1 | a0001c0001t0001g0016 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.215+16797G>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76039191 | ||||||
chr14:76039252
|
C | T | 1 | a0001c0001t0001g0045 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.215+16858C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76039252 | ||||||
chr14:76039259
|
A | G | 1 | a0001c0001t0001g0373 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.215+16865A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76039259 | ||||||
chr14:76039268
|
G | A | 3 | a0001c0001t0001g0215a0001c0001t0001g0228a0001c0001t0001g0229 | 3 | HG01256.hp1 HG01258.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.215+16874G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76039268 | ||||||
chr14:76039315
|
T | C | 297 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(294): Show | 304 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(301): Show |
intron_variant | MODIFIER | c.215+16921T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76039315 | ||||||
chr14:76039320
|
G | A | 1 | a0001c0001t0001g0221 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.215+16926G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76039320 | ||||||
chr14:76039327
|
T | C | 1 | a0001c0001t0001g0163 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.215+16933T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76039327 | ||||||
chr14:76039407
|
C | A | 1 | a0001c0001t0001g0179 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.215+17013C>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76039407 | ||||||
chr14:76039570
|
A | T | 16 | a0001c0001t0001g0035a0001c0001t0001g0037a0001c0001t0001g0038others(13): Show | 16 | HG01928.hp2 HG01943.hp1 HG01975.hp2 others(13): Show |
intron_variant | MODIFIER | c.215+17176A>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76039570 | ||||||
chr14:76039610
|
C | T | 7 | a0001c0001t0001g0317a0001c0001t0001g0328a0001c0001t0001g0331others(4): Show | 7 | HG00673.hp2 HG02132.hp1 NA18949.hp2 others(4): Show |
intron_variant | MODIFIER | c.215+17216C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76039610 | ||||||
chr14:76040301
|
G | A | 10 | a0001c0001t0001g0020a0001c0001t0001g0023a0001c0001t0001g0024others(7): Show | 10 | HG01243.hp1 HG01884.hp2 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.215+17907G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76040301 | ||||||
chr14:76040385
|
T | C | 10 | a0001c0001t0001g0020a0001c0001t0001g0023a0001c0001t0001g0024others(7): Show | 10 | HG01243.hp1 HG01884.hp2 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.215+17991T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76040385 | ||||||
chr14:76040523
|
T | C | 2 | a0001c0001t0001g0100a0001c0001t0001g0265 | 2 | HG01891.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.216-18119T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76040523 | ||||||
chr14:76040709
|
C | G | 7 | a0001c0001t0001g0019a0001c0001t0001g0125a0001c0001t0001g0128others(4): Show | 7 | HG01952.hp2 HG02004.hp2 NA18967.hp2 others(4): Show |
intron_variant | MODIFIER | c.216-17933C>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76040709 | ||||||
chr14:76040779
|
G | A | 1 | a0001c0001t0001g0307 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.216-17863G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76040779 | ||||||
chr14:76040801
|
G | T | 4 | a0001c0001t0001g0300a0001c0001t0001g0377a0001c0001t0001g0378others(1): Show | 4 | NA18950.hp1 NA18961.hp1 NA19056.hp1 others(1): Show |
intron_variant | MODIFIER | c.216-17841G>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76040801 | ||||||
chr14:76040840
|
C | G | 2 | a0001c0001t0001g0117a0001c0001t0001g0118 | 2 | HG02486.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.216-17802C>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76040840 | ||||||
chr14:76040898
|
G | T | 2 | a0001c0001t0001g0377a0001c0001t0001g0379 | 2 | NA18950.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.216-17744G>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76040898 | ||||||
chr14:76040956
|
C | A | 80 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0017others(77): Show | 82 | HG00438.hp2 HG00642.hp2 HG01070.hp1 others(79): Show |
intron_variant | MODIFIER | c.216-17686C>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76040956 | ||||||
chr14:76041116
|
A | G | 42 | a0001c0001t0001g0010a0001c0001t0001g0017a0001c0001t0001g0097others(39): Show | 43 | HG00438.hp2 HG00642.hp2 HG01070.hp1 others(40): Show |
intron_variant | MODIFIER | c.216-17526A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76041116 | ||||||
chr14:76041161
|
G | A | 6 | a0001c0001t0001g0106a0001c0001t0001g0283a0001c0001t0001g0291others(3): Show | 6 | HG01433.hp1 HG01496.hp1 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.216-17481G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76041161 | ||||||
chr14:76041391
|
T | G | 5 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0058others(2): Show | 5 | HG01243.hp1 HG01884.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.216-17251T>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76041391 | ||||||
chr14:76041491
|
A | G | 293 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(290): Show | 300 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(297): Show |
intron_variant | MODIFIER | c.216-17151A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76041491 | ||||||
chr14:76041539
|
C | T | 1 | a0001c0001t0001g0373 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.216-17103C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76041539 | ||||||
chr14:76041576
|
T | C | 9 | a0001c0001t0001g0074a0001c0001t0001g0092a0001c0001t0001g0093others(6): Show | 9 | HG02109.hp2 HG02572.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.216-17066T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76041576 | ||||||
chr14:76041717
|
C | T | 1 | a0001c0001t0001g0013 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.216-16925C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76041717 | ||||||
chr14:76041750
|
G | T | 1 | a0001c0001t0001g0342 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.216-16892G>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76041750 | ||||||
chr14:76041750
|
GT | G | 294 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(291): Show | 301 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(298): Show |
intron_variant | MODIFIER | c.216-16882delT | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr14 | 76041750 | |||||
chr14:76041752
|
T | C | 96 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(93): Show | 99 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(96): Show |
intron_variant | MODIFIER | c.216-16890T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76041752 | ||||||
chr14:76042073
|
G | A | 1 | a0001c0001t0001g0290 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.216-16569G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76042073 | ||||||
chr14:76042104
|
G | A | 1 | a0001c0001t0001g0056 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.216-16538G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76042104 | ||||||
chr14:76042107
|
G | GAC | 114 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(111): Show | 118 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.216-16516_216-1651 others(6): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr14 | 76042107 | |||||
chr14:76042107
|
G | GACAC | 3 | a0001c0001t0001g0138a0001c0001t0001g0176a0001c0001t0001g0180 | 3 | HG01081.hp2 HG01255.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.216-16518_216-1651 others(8): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr14 | 76042107 | |||||
chr14:76042127
|
C | CAT | 4 | a0001c0001t0001g0135a0001c0001t0001g0210a0001c0001t0001g0211others(1): Show | 4 | HG01358.hp2 HG01516.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.216-16515_216-1651 others(6): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76042127 | ||||||
chr14:76042257
|
T | TA | 6 | a0001c0001t0001g0103a0001c0001t0001g0155a0001c0001t0001g0162others(3): Show | 6 | NA18953.hp2 NA18972.hp1 NA18974.hp1 others(3): Show |
intron_variant | MODIFIER | c.216-16369dupA | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr14 | 76042257 | |||||
chr14:76042289
|
C | G | 1 | a0001c0001t0001g0176 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.216-16353C>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76042289 | ||||||
chr14:76042427
|
G | A | 111 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0013others(108): Show | 113 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(110): Show |
intron_variant | MODIFIER | c.216-16215G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76042427 | ||||||
chr14:76042436
|
C | A | 7 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0368others(4): Show | 7 | HG01109.hp2 HG02486.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.216-16206C>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76042436 | ||||||
chr14:76042469
|
A | G | 2 | a0001c0001t0001g0012a0001c0001t0001g0373 | 3 | HG03491.hp2 HG03492.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.216-16173A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76042469 | ||||||
chr14:76042547
|
G | A | 2 | a0001c0001t0001g0012a0001c0001t0001g0373 | 3 | HG03491.hp2 HG03492.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.216-16095G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76042547 | ||||||
chr14:76042629
|
T | C | 11 | a0001c0001t0001g0012a0001c0001t0001g0020a0001c0001t0001g0023others(8): Show | 12 | HG01243.hp1 HG01884.hp2 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.216-16013T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76042629 | ||||||
chr14:76042702
|
C | T | 2 | a0001c0001t0001g0012a0001c0001t0001g0373 | 3 | HG03491.hp2 HG03492.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.216-15940C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76042702 | ||||||
chr14:76043023
|
G | A | 1 | a0001c0001t0001g0171 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.216-15619G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76043023 | ||||||
chr14:76043153
|
G | C | 1 | a0001c0001t0001g0373 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.216-15489G>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76043153 | ||||||
chr14:76043227
|
T | G | 4 | a0001c0001t0001g0065a0001c0001t0001g0246a0001c0001t0001g0247others(1): Show | 4 | HG02258.hp1 HG02622.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.216-15415T>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76043227 | ||||||
chr14:76043369
|
C | CTCGTG | 107 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0017others(104): Show | 109 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.216-15271_216-1526 others(9): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr14 | 76043369 | |||||
chr14:76043471
|
A | AT | 6 | a0001c0001t0001g0012a0001c0001t0001g0114a0001c0001t0001g0115others(3): Show | 7 | HG01192.hp2 HG02055.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.216-15158dupT | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr14 | 76043471 | |||||
chr14:76043471
|
A | ATT | 6 | a0001c0001t0001g0020a0001c0001t0001g0023a0001c0001t0001g0024others(3): Show | 6 | HG01243.hp1 HG01884.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.216-15159_216-1515 others(6): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr14 | 76043471 | |||||
chr14:76043490
|
G | A | 1 | a0001c0001t0001g0016 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.216-15152G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76043490 | ||||||
chr14:76043490
|
G | C | 1 | a0001c0001t0001g0135 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.216-15152G>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76043490 | ||||||
chr14:76043525
|
G | T | 94 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(91): Show | 97 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(94): Show |
intron_variant | MODIFIER | c.216-15117G>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76043525 | ||||||
chr14:76043526
|
G | A | 5 | a0001c0001t0001g0327a0001c0001t0001g0333a0001c0001t0001g0354others(2): Show | 5 | NA18974.hp2 NA18981.hp2 NA18998.hp1 others(2): Show |
intron_variant | MODIFIER | c.216-15116G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76043526 | ||||||
chr14:76043568
|
G | A | 1 | a0001c0001t0001g0142 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.216-15074G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76043568 | ||||||
chr14:76043690
|
T | C | 1 | a0001c0001t0001g0303 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.216-14952T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76043690 | ||||||
chr14:76043818
|
A | G | 57 | a0001c0001t0001g0004a0001c0001t0001g0021a0001c0001t0001g0022others(54): Show | 58 | HG00099.hp1 HG00408.hp2 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.216-14824A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76043818 | ||||||
chr14:76043877
|
G | A | 1 | a0001c0001t0001g0016 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.216-14765G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76043877 | ||||||
chr14:76043898
|
C | T | 1 | a0001c0001t0001g0097 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.216-14744C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76043898 | ||||||
chr14:76044052
|
T | C | 4 | a0001c0001t0001g0013a0001c0001t0001g0066a0001c0001t0001g0227others(1): Show | 4 | HG01167.hp1 HG02965.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.216-14590T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76044052 | ||||||
chr14:76044143
|
G | A | 4 | a0001c0001t0001g0013a0001c0001t0001g0066a0001c0001t0001g0227others(1): Show | 4 | HG01167.hp1 HG02965.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.216-14499G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76044143 | ||||||
chr14:76044193
|
C | A | 1 | a0001c0001t0001g0066 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.216-14449C>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76044193 | ||||||
chr14:76044198
|
C | A | 1 | a0001c0001t0001g0297 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.216-14444C>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76044198 | ||||||
chr14:76044260
|
G | A | 2 | a0001c0001t0001g0020a0001c0001t0001g0038 | 2 | NA19070.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.216-14382G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76044260 | ||||||
chr14:76044320
|
G | A | 3 | a0001c0001t0001g0167a0001c0001t0001g0171a0001c0001t0001g0244 | 3 | HG01109.hp1 HG01192.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.216-14322G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76044320 | ||||||
chr14:76044347
|
A | G | 1 | a0001c0001t0001g0166 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.216-14295A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76044347 | ||||||
chr14:76044660
|
C | A | 1 | a0001c0001t0001g0005 | 2 | HG01070.hp2 HG01934.hp1 |
intron_variant | MODIFIER | c.216-13982C>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76044660 | ||||||
chr14:76044702
|
G | T | 6 | a0001c0001t0001g0020a0001c0001t0001g0023a0001c0001t0001g0024others(3): Show | 6 | HG01243.hp1 HG01884.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.216-13940G>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76044702 | ||||||
chr14:76044712
|
A | T | 4 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0373others(1): Show | 4 | HG02055.hp1 HG02280.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.216-13930A>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76044712 | ||||||
chr14:76044777
|
G | A | 1 | a0001c0001t0001g0373 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.216-13865G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76044777 | ||||||
chr14:76044797
|
T | C | 283 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(280): Show | 290 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(287): Show |
intron_variant | MODIFIER | c.216-13845T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76044797 | ||||||
chr14:76044963
|
C | T | 272 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(269): Show | 278 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(275): Show |
intron_variant | MODIFIER | c.216-13679C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76044963 | ||||||
chr14:76045052
|
T | C | 3 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0380 | 3 | HG02055.hp1 HG02280.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.216-13590T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76045052 | ||||||
chr14:76045185
|
G | A | 10 | a0001c0001t0001g0009a0001c0001t0001g0013a0001c0001t0001g0105others(7): Show | 11 | HG01884.hp1 HG01891.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.216-13457G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76045185 | ||||||
chr14:76045191
|
A | T | 1 | a0001c0001t0001g0016 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.216-13451A>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76045191 | ||||||
chr14:76045363
|
G | A | 59 | a0001c0001t0001g0004a0001c0001t0001g0021a0001c0001t0001g0022others(56): Show | 60 | HG00099.hp1 HG00408.hp2 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.216-13279G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76045363 | ||||||
chr14:76045455
|
A | G | 26 | a0001c0001t0001g0010a0001c0001t0001g0017a0001c0001t0001g0097others(23): Show | 27 | HG00642.hp2 HG01123.hp2 HG01261.hp2 others(24): Show |
intron_variant | MODIFIER | c.216-13187A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76045455 | ||||||
chr14:76045631
|
G | A | 1 | a0001c0001t0001g0234 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.216-13011G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76045631 | ||||||
chr14:76045654
|
C | T | 1 | a0001c0001t0001g0373 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.216-12988C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76045654 | ||||||
chr14:76045655
|
G | A | 2 | a0001c0001t0001g0104a0001c0001t0001g0227 | 2 | HG01167.hp1 HG02602.hp2 |
intron_variant | MODIFIER | c.216-12987G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76045655 | ||||||
chr14:76045655
|
G | T | 2 | a0001c0001t0001g0171a0001c0001t0001g0244 | 2 | HG01192.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.216-12987G>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76045655 | ||||||
chr14:76045782
|
G | A | 1 | a0001c0001t0001g0192 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.216-12860G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76045782 | ||||||
chr14:76045803
|
T | G | 7 | a0001c0001t0001g0020a0001c0001t0001g0023a0001c0001t0001g0024others(4): Show | 7 | HG01243.hp1 HG01884.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.216-12839T>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76045803 | ||||||
chr14:76045955
|
G | A | 292 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(289): Show | 299 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(296): Show |
intron_variant | MODIFIER | c.216-12687G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76045955 | ||||||
chr14:76045997
|
T | A | 1 | a0001c0001t0001g0054 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.216-12645T>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76045997 | ||||||
chr14:76046271
|
C | A | 4 | a0001c0001t0001g0276a0001c0001t0001g0277a0001c0001t0001g0278others(1): Show | 4 | NA18943.hp2 NA18955.hp2 NA18966.hp1 others(1): Show |
intron_variant | MODIFIER | c.216-12371C>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76046271 | ||||||
chr14:76046297
|
G | C | 1 | a0001c0001t0001g0328 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.216-12345G>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76046297 | ||||||
chr14:76046447
|
G | T | 1 | a0001c0001t0001g0363 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.216-12195G>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76046447 | ||||||
chr14:76046537
|
A | G | 1 | a0001c0001t0001g0359 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.216-12105A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76046537 | ||||||
chr14:76046818
|
A | G | 1 | a0001c0001t0001g0066 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.216-11824A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76046818 | ||||||
chr14:76046904
|
A | C | 105 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0017others(102): Show | 107 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.216-11738A>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76046904 | ||||||
chr14:76046933
|
C | G | 1 | a0001c0001t0001g0182 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.216-11709C>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76046933 | ||||||
chr14:76046982
|
A | T | 1 | a0001c0001t0001g0182 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.216-11660A>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76046982 | ||||||
chr14:76047031
|
G | A | 1 | a0001c0001t0001g0016 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.216-11611G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76047031 | ||||||
chr14:76047249
|
G | C | 3 | a0001c0001t0001g0125a0001c0001t0001g0128a0001c0001t0001g0130 | 3 | NA18967.hp2 NA18982.hp2 NA18997.hp2 |
intron_variant | MODIFIER | c.216-11393G>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76047249 | ||||||
chr14:76047334
|
T | C | 295 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(292): Show | 302 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(299): Show |
intron_variant | MODIFIER | c.216-11308T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76047334 | ||||||
chr14:76047420
|
G | A | 1 | a0001c0001t0001g0222 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.216-11222G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76047420 | ||||||
chr14:76047703
|
G | A | 9 | a0001c0001t0001g0020a0001c0001t0001g0023a0001c0001t0001g0024others(6): Show | 9 | HG01243.hp1 HG01884.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.216-10939G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76047703 | ||||||
chr14:76047733
|
C | CT | 17 | a0001c0001t0001g0018a0001c0001t0001g0028a0001c0001t0001g0033others(14): Show | 17 | HG00597.hp1 HG01074.hp1 HG01109.hp2 others(14): Show |
intron_variant | MODIFIER | c.216-10894dupT | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr14 | 76047733 | |||||
chr14:76047970
|
C | A | 27 | a0001c0001t0001g0201a0001c0001t0001g0202a0001c0001t0001g0203others(24): Show | 27 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(24): Show |
intron_variant | MODIFIER | c.216-10672C>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76047970 | ||||||
chr14:76047979
|
G | T | 105 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0017others(102): Show | 107 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.216-10663G>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76047979 | ||||||
chr14:76048125
|
G | A | 37 | a0001c0001t0001g0003a0001c0001t0001g0025a0001c0001t0001g0026others(34): Show | 38 | HG01074.hp1 HG01081.hp1 HG01243.hp2 others(35): Show |
intron_variant | MODIFIER | c.216-10517G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76048125 | ||||||
chr14:76048142
|
T | C | 1 | a0001c0001t0001g0153 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.216-10500T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76048142 | ||||||
chr14:76048147
|
C | T | 2 | a0001c0001t0001g0039a0001c0001t0001g0373 | 2 | HG03688.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.216-10495C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76048147 | ||||||
chr14:76048242
|
C | T | 7 | a0001c0001t0001g0020a0001c0001t0001g0023a0001c0001t0001g0024others(4): Show | 7 | HG01243.hp1 HG01884.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.216-10400C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76048242 | ||||||
chr14:76048681
|
C | T | 269 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(266): Show | 275 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(272): Show |
intron_variant | MODIFIER | c.216-9961C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76048681 | ||||||
chr14:76048691
|
A | T | 3 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0380 | 3 | HG02055.hp1 HG02280.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.216-9951A>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76048691 | ||||||
chr14:76048830
|
C | T | 1 | a0001c0001t0001g0219 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.216-9812C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76048830 | ||||||
chr14:76048860
|
G | A | 2 | a0001c0001t0001g0028a0001c0001t0001g0150 | 2 | HG02280.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.216-9782G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76048860 | ||||||
chr14:76048870
|
C | T | 1 | a0001c0001t0001g0256 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.216-9772C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76048870 | ||||||
chr14:76048881
|
T | A | 9 | a0001c0001t0001g0009a0001c0001t0001g0105a0001c0001t0001g0251others(6): Show | 10 | HG01884.hp1 HG01891.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.216-9761T>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76048881 | ||||||
chr14:76048890
|
A | G | 295 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(292): Show | 302 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(299): Show |
intron_variant | MODIFIER | c.216-9752A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76048890 | ||||||
chr14:76048970
|
A | G | 37 | a0001c0001t0001g0020a0001c0001t0001g0023a0001c0001t0001g0024others(34): Show | 37 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(34): Show |
intron_variant | MODIFIER | c.216-9672A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76048970 | ||||||
chr14:76048996
|
C | T | 111 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0017others(108): Show | 113 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(110): Show |
intron_variant | MODIFIER | c.216-9646C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76048996 | ||||||
chr14:76049191
|
A | G | 2 | a0001c0001t0001g0191a0001c0001t0001g0194 | 2 | NA18950.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.216-9451A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76049191 | ||||||
chr14:76049216
|
C | A | 3 | a0001c0001t0001g0157a0001c0001t0001g0158a0001c0001t0001g0164 | 3 | NA18946.hp2 NA18964.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.216-9426C>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76049216 | ||||||
chr14:76049223
|
T | C | 2 | a0001c0001t0001g0311a0001c0001t0001g0312 | 2 | NA18747.hp2 NA19055.hp1 |
intron_variant | MODIFIER | c.216-9419T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76049223 | ||||||
chr14:76049408
|
A | G | 1 | a0001c0001t0001g0013 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.216-9234A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76049408 | ||||||
chr14:76049457
|
GT | G | 189 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(186): Show | 194 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(191): Show |
intron_variant | MODIFIER | c.216-9171delT | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr14 | 76049457 | |||||
chr14:76049457
|
GTT | G | 109 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0020others(106): Show | 111 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(108): Show |
intron_variant | MODIFIER | c.216-9172_216-9171d others(4): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr14 | 76049457 | |||||
chr14:76049460
|
T | G | 33 | a0001c0001t0001g0020a0001c0001t0001g0023a0001c0001t0001g0024others(30): Show | 33 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(30): Show |
intron_variant | MODIFIER | c.216-9182T>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76049460 | ||||||
chr14:76049461
|
T | G | 2 | a0001c0001t0001g0368a0001c0001t0001g0369 | 2 | HG01109.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.216-9181T>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76049461 | ||||||
chr14:76049486
|
A | G | 22 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0101others(19): Show | 28 | HG01256.hp2 HG01943.hp2 HG01952.hp1 others(25): Show |
intron_variant | MODIFIER | c.216-9156A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76049486 | ||||||
chr14:76049517
|
G | A | 115 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0017others(112): Show | 117 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(114): Show |
intron_variant | MODIFIER | c.216-9125G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76049517 | ||||||
chr14:76049532
|
A | T | 1 | a0001c0001t0001g0207 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.216-9110A>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76049532 | ||||||
chr14:76049728
|
A | ACTT | 303 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(300): Show | 310 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(307): Show |
intron_variant | MODIFIER | c.216-8912_216-8910d others(5): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr14 | 76049728 | |||||
chr14:76049866
|
G | GC | 105 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0017others(102): Show | 107 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.216-8771dupC | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr14 | 76049866 | |||||
chr14:76050078
|
G | A | 295 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(292): Show | 302 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(299): Show |
intron_variant | MODIFIER | c.216-8564G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76050078 | ||||||
chr14:76050199
|
C | T | 5 | a0001c0001t0001g0320a0001c0001t0001g0321a0001c0001t0001g0322others(2): Show | 5 | HG00735.hp1 HG01981.hp1 HG02148.hp2 others(2): Show |
intron_variant | MODIFIER | c.216-8443C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76050199 | ||||||
chr14:76050219
|
C | T | 1 | a0001c0001t0001g0313 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.216-8423C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76050219 | ||||||
chr14:76050403
|
G | T | 2 | a0001c0001t0001g0314a0001c0001t0001g0315 | 2 | HG03017.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.216-8239G>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76050403 | ||||||
chr14:76050429
|
T | G | 116 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0012others(113): Show | 119 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(116): Show |
intron_variant | MODIFIER | c.216-8213T>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76050429 | ||||||
chr14:76050458
|
T | C | 8 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0146others(5): Show | 8 | HG02056.hp1 HG02132.hp2 NA18951.hp1 others(5): Show |
intron_variant | MODIFIER | c.216-8184T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76050458 | ||||||
chr14:76050519
|
G | T | 1 | a0001c0001t0001g0227 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.216-8123G>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76050519 | ||||||
chr14:76050606
|
A | T | 1 | a0001c0001t0001g0213 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.216-8036A>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76050606 | ||||||
chr14:76050627
|
TGA | T | 6 | a0001c0001t0001g0020a0001c0001t0001g0023a0001c0001t0001g0024others(3): Show | 6 | HG01243.hp1 HG01884.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.216-8011_216-8010d others(4): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr14 | 76050627 | |||||
chr14:76050633
|
T | G | 1 | a0001c0001t0001g0048 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.216-8009T>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76050633 | ||||||
chr14:76050703
|
C | T | 18 | a0001c0001t0001g0009a0001c0001t0001g0013a0001c0001t0001g0036others(15): Show | 19 | HG01884.hp1 HG01891.hp2 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.216-7939C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76050703 | ||||||
chr14:76050820
|
G | A | 105 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0017others(102): Show | 107 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.216-7822G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76050820 | ||||||
chr14:76050821
|
G | C | 115 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0017others(112): Show | 117 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(114): Show |
intron_variant | MODIFIER | c.216-7821G>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76050821 | ||||||
chr14:76051009
|
G | A | 7 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0368others(4): Show | 7 | HG01109.hp2 HG02486.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.216-7633G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76051009 | ||||||
chr14:76051024
|
T | A | 1 | a0001c0001t0001g0373 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.216-7618T>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76051024 | ||||||
chr14:76051104
|
G | C | 1 | a0001c0001t0001g0013 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.216-7538G>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76051104 | ||||||
chr14:76051108
|
T | C | 1 | a0001c0001t0001g0066 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.216-7534T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76051108 | ||||||
chr14:76051219
|
G | A | 1 | a0001c0001t0001g0288 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.216-7423G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76051219 | ||||||
chr14:76051457
|
G | A | 1 | a0001c0001t0001g0360 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.216-7185G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76051457 | ||||||
chr14:76051502
|
T | C | 1 | a0001c0001t0001g0025 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.216-7140T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76051502 | ||||||
chr14:76051622
|
C | T | 115 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0017others(112): Show | 117 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(114): Show |
intron_variant | MODIFIER | c.216-7020C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76051622 | ||||||
chr14:76051903
|
G | A | 1 | a0001c0001t0001g0114 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.216-6739G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76051903 | ||||||
chr14:76051944
|
C | A | 105 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0017others(102): Show | 107 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.216-6698C>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76051944 | ||||||
chr14:76051996
|
C | T | 9 | a0001c0001t0001g0074a0001c0001t0001g0092a0001c0001t0001g0093others(6): Show | 9 | HG02109.hp2 HG02572.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.216-6646C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76051996 | ||||||
chr14:76052047
|
C | T | 2 | a0001c0001t0001g0191a0001c0001t0001g0194 | 2 | NA18950.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.216-6595C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76052047 | ||||||
chr14:76052305
|
A | G | 4 | a0001c0001t0001g0156a0001c0001t0001g0162a0001c0001t0001g0185others(1): Show | 4 | NA18939.hp1 NA18974.hp1 NA18999.hp2 others(1): Show |
intron_variant | MODIFIER | c.216-6337A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76052305 | ||||||
chr14:76052317
|
G | A | 295 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(292): Show | 302 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(299): Show |
intron_variant | MODIFIER | c.216-6325G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76052317 | ||||||
chr14:76052584
|
C | T | 3 | a0001c0001t0001g0220a0001c0001t0001g0225a0001c0001t0001g0233 | 3 | HG02165.hp1 NA18978.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.216-6058C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76052584 | ||||||
chr14:76052787
|
G | A | 1 | a0001c0001t0001g0373 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.216-5855G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76052787 | ||||||
chr14:76052790
|
G | A | 93 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(90): Show | 96 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.216-5852G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76052790 | ||||||
chr14:76052803
|
A | G | 2 | a0001c0001t0001g0036a0001c0001t0001g0077 | 2 | HG02572.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.216-5839A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76052803 | ||||||
chr14:76053031
|
A | G | 4 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0048others(1): Show | 4 | HG01928.hp2 HG01943.hp1 HG01993.hp2 others(1): Show |
intron_variant | MODIFIER | c.216-5611A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76053031 | ||||||
chr14:76053076
|
G | A | 2 | a0001c0001t0001g0034a0001c0001t0001g0132 | 2 | NA19240.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.216-5566G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76053076 | ||||||
chr14:76053312
|
A | G | 126 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0017others(123): Show | 128 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(125): Show |
intron_variant | MODIFIER | c.216-5330A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76053312 | ||||||
chr14:76053385
|
A | G | 122 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0017others(119): Show | 124 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(121): Show |
intron_variant | MODIFIER | c.216-5257A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76053385 | ||||||
chr14:76053462
|
A | G | 126 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0017others(123): Show | 128 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(125): Show |
intron_variant | MODIFIER | c.216-5180A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76053462 | ||||||
chr14:76053499
|
C | T | 1 | a0001c0001t0001g0025 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.216-5143C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76053499 | ||||||
chr14:76053572
|
G | A | 55 | a0001c0001t0001g0004a0001c0001t0001g0021a0001c0001t0001g0022others(52): Show | 56 | HG00099.hp1 HG00408.hp2 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.216-5070G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76053572 | ||||||
chr14:76053633
|
C | T | 1 | a0001c0001t0001g0297 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.216-5009C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76053633 | ||||||
chr14:76053634
|
G | T | 1 | a0001c0001t0001g0076 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.216-5008G>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76053634 | ||||||
chr14:76053650
|
A | G | 1 | a0001c0001t0001g0299 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.216-4992A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76053650 | ||||||
chr14:76053733
|
A | C | 1 | a0001c0001t0001g0283 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.216-4909A>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76053733 | ||||||
chr14:76053844
|
G | T | 1 | a0001c0001t0001g0013 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.216-4798G>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76053844 | ||||||
chr14:76054026
|
C | A | 294 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(291): Show | 301 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(298): Show |
intron_variant | MODIFIER | c.216-4616C>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76054026 | ||||||
chr14:76054081
|
A | G | 1 | a0001c0001t0001g0283 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.216-4561A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76054081 | ||||||
chr14:76054176
|
G | A | 1 | a0001c0001t0001g0373 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.216-4466G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76054176 | ||||||
chr14:76054256
|
G | C | 4 | a0001c0001t0001g0065a0001c0001t0001g0246a0001c0001t0001g0247others(1): Show | 4 | HG02258.hp1 HG02622.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.216-4386G>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76054256 | ||||||
chr14:76054304
|
A | G | 110 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0017others(107): Show | 112 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(109): Show |
intron_variant | MODIFIER | c.216-4338A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76054304 | ||||||
chr14:76054416
|
G | C | 1 | a0001c0001t0001g0282 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.216-4226G>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76054416 | ||||||
chr14:76054495
|
T | A | 1 | a0001c0001t0001g0290 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.216-4147T>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76054495 | ||||||
chr14:76054503
|
A | G | 1 | a0001c0001t0001g0290 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.216-4139A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76054503 | ||||||
chr14:76054536
|
G | A | 3 | a0001c0001t0001g0138a0001c0001t0001g0176a0001c0001t0001g0180 | 3 | HG01081.hp2 HG01255.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.216-4106G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76054536 | ||||||
chr14:76054546
|
T | C | 1 | a0001c0001t0001g0373 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.216-4096T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76054546 | ||||||
chr14:76054657
|
G | A | 9 | a0001c0001t0001g0074a0001c0001t0001g0092a0001c0001t0001g0093others(6): Show | 9 | HG02109.hp2 HG02572.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.216-3985G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76054657 | ||||||
chr14:76054667
|
T | C | 1 | a0001c0001t0001g0305 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.216-3975T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76054667 | ||||||
chr14:76054724
|
G | T | 6 | a0001c0001t0001g0020a0001c0001t0001g0023a0001c0001t0001g0024others(3): Show | 6 | HG01243.hp1 HG01884.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.216-3918G>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76054724 | ||||||
chr14:76055065
|
C | A | 1 | a0001c0001t0001g0114 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.216-3577C>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76055065 | ||||||
chr14:76055076
|
G | A | 55 | a0001c0001t0001g0004a0001c0001t0001g0021a0001c0001t0001g0022others(52): Show | 56 | HG00099.hp1 HG00408.hp2 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.216-3566G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76055076 | ||||||
chr14:76055216
|
C | T | 1 | a0001c0001t0001g0025 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.216-3426C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76055216 | ||||||
chr14:76055232
|
GCTA | G | 3 | a0002c0002t0001g0356a0002c0002t0001g0357a0002c0002t0001g0362 | 3 | HG02056.hp2 NA18995.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.216-3407_216-3405d others(5): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr14 | 76055232 | |||||
chr14:76055267
|
A | G | 295 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(292): Show | 302 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(299): Show |
intron_variant | MODIFIER | c.216-3375A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76055267 | ||||||
chr14:76055278
|
T | C | 1 | a0001c0001t0001g0013 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.216-3364T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76055278 | ||||||
chr14:76055310
|
C | A | 41 | a0001c0001t0001g0010a0001c0001t0001g0017a0001c0001t0001g0097others(38): Show | 42 | HG00438.hp2 HG00642.hp2 HG01070.hp1 others(39): Show |
intron_variant | MODIFIER | c.216-3332C>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76055310 | ||||||
chr14:76055429
|
A | G | 296 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(293): Show | 303 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(300): Show |
intron_variant | MODIFIER | c.216-3213A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76055429 | ||||||
chr14:76055467
|
G | T | 1 | a0001c0001t0001g0303 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.216-3175G>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76055467 | ||||||
chr14:76055470
|
T | C | 2 | a0001c0001t0001g0334a0001c0001t0001g0338 | 2 | NA18941.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.216-3172T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76055470 | ||||||
chr14:76055487
|
A | G | 3 | a0001c0001t0001g0024a0001c0001t0001g0058a0001c0001t0001g0060 | 3 | HG02895.hp2 HG02965.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.216-3155A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76055487 | ||||||
chr14:76055511
|
A | T | 1 | a0001c0001t0001g0373 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.216-3131A>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76055511 | ||||||
chr14:76055535
|
C | A | 330 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(327): Show | 343 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(340): Show |
intron_variant | MODIFIER | c.216-3107C>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76055535 | ||||||
chr14:76055684
|
A | G | 6 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0121others(3): Show | 6 | HG00609.hp2 NA18964.hp1 NA18967.hp1 others(3): Show |
intron_variant | MODIFIER | c.216-2958A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76055684 | ||||||
chr14:76055737
|
C | T | 1 | a0001c0001t0001g0330 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.216-2905C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76055737 | ||||||
chr14:76055856
|
G | T | 3 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0380 | 3 | HG02055.hp1 HG02280.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.216-2786G>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76055856 | ||||||
chr14:76055951
|
G | A | 2 | a0001c0001t0001g0168a0001c0001t0001g0170 | 2 | NA18984.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.216-2691G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76055951 | ||||||
chr14:76055961
|
A | G | 1 | a0001c0001t0001g0029 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.216-2681A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76055961 | ||||||
chr14:76056020
|
A | C | 1 | a0001c0001t0001g0256 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.216-2622A>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76056020 | ||||||
chr14:76056036
|
T | G | 6 | a0001c0001t0001g0017a0001c0001t0001g0267a0001c0001t0001g0268others(3): Show | 6 | HG01123.hp2 HG01361.hp1 HG02273.hp1 others(3): Show |
intron_variant | MODIFIER | c.216-2606T>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76056036 | ||||||
chr14:76056269
|
C | G | 9 | a0001c0001t0001g0074a0001c0001t0001g0092a0001c0001t0001g0093others(6): Show | 9 | HG02109.hp2 HG02572.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.216-2373C>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76056269 | ||||||
chr14:76056289
|
C | T | 1 | a0001c0001t0001g0192 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.216-2353C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76056289 | ||||||
chr14:76056290
|
G | A | 1 | a0001c0001t0001g0142 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.216-2352G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76056290 | ||||||
chr14:76056309
|
G | A | 4 | a0001c0001t0001g0065a0001c0001t0001g0246a0001c0001t0001g0247others(1): Show | 4 | HG02258.hp1 HG02622.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.216-2333G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76056309 | ||||||
chr14:76056415
|
A | G | 3 | a0001c0001t0001g0157a0001c0001t0001g0158a0001c0001t0001g0164 | 3 | NA18946.hp2 NA18964.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.216-2227A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76056415 | ||||||
chr14:76056535
|
G | T | 2 | a0001c0001t0001g0117a0001c0001t0001g0118 | 2 | HG02486.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.216-2107G>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76056535 | ||||||
chr14:76056543
|
T | A | 1 | a0001c0001t0001g0169 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.216-2099T>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76056543 | ||||||
chr14:76056848
|
G | A | 1 | a0001c0001t0001g0283 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.216-1794G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76056848 | ||||||
chr14:76056851
|
C | T | 2 | a0001c0001t0001g0091a0001c0001t0001g0104 | 2 | HG02602.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.216-1791C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76056851 | ||||||
chr14:76056984
|
T | C | 330 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(327): Show | 343 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(340): Show |
intron_variant | MODIFIER | c.216-1658T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76056984 | ||||||
chr14:76057010
|
A | G | 1 | a0001c0001t0001g0066 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.216-1632A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76057010 | ||||||
chr14:76057242
|
A | AT | 126 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0017others(123): Show | 128 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(125): Show |
intron_variant | MODIFIER | c.216-1392dupT | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr14 | 76057242 | |||||
chr14:76057274
|
T | C | 126 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0017others(123): Show | 128 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(125): Show |
intron_variant | MODIFIER | c.216-1368T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76057274 | ||||||
chr14:76057287
|
A | G | 1 | a0001c0001t0001g0210 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.216-1355A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76057287 | ||||||
chr14:76057293
|
G | A | 5 | a0001c0001t0001g0035a0001c0001t0001g0037a0001c0001t0001g0039others(2): Show | 5 | NA18960.hp1 NA18963.hp1 NA18991.hp2 others(2): Show |
intron_variant | MODIFIER | c.216-1349G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76057293 | ||||||
chr14:76057438
|
A | G | 125 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0017others(122): Show | 127 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(124): Show |
intron_variant | MODIFIER | c.216-1204A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76057438 | ||||||
chr14:76057553
|
CA | C | 302 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(299): Show | 309 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(306): Show |
intron_variant | MODIFIER | c.216-1075delA | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr14 | 76057553 | |||||
chr14:76057680
|
G | A | 1 | a0001c0001t0001g0119 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.216-962G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76057680 | ||||||
chr14:76057901
|
A | G | 1 | a0001c0001t0001g0373 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.216-741A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76057901 | ||||||
chr14:76057960
|
T | TA | 6 | a0001c0001t0001g0020a0001c0001t0001g0023a0001c0001t0001g0024others(3): Show | 6 | HG01243.hp1 HG01884.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.216-677dupA | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr14 | 76057960 | |||||
chr14:76057966
|
T | G | 6 | a0001c0001t0001g0020a0001c0001t0001g0023a0001c0001t0001g0024others(3): Show | 6 | HG01243.hp1 HG01884.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.216-676T>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76057966 | ||||||
chr14:76058081
|
C | T | 1 | a0001c0001t0001g0288 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.216-561C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76058081 | ||||||
chr14:76058106
|
C | T | 1 | a0001c0001t0001g0280 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.216-536C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76058106 | ||||||
chr14:76058332
|
A | T | 1 | a0001c0001t0001g0203 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.216-310A>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76058332 | ||||||
chr14:76058450
|
G | T | 11 | a0001c0001t0001g0009a0001c0001t0001g0036a0001c0001t0001g0077others(8): Show | 12 | HG01884.hp1 HG01891.hp2 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.216-192G>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76058450 | ||||||
chr14:76058625
|
T | G | 8 | a0001c0001t0001g0074a0001c0001t0001g0092a0001c0001t0001g0093others(5): Show | 8 | HG02109.hp2 HG02572.hp1 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.216-17T>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76058625 | ||||||
chr14:76058627
|
CT | C | 130 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0017others(127): Show | 132 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(129): Show |
splice_region_variant&intron_variant | LOW | c.216-4delT | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr14 | 76058627 | |||||
chr14:76059033
|
T | C | 1 | a0001c0001t0001g0373 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.249-294T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 4/8 | chr14 | 76059033 | ||||||
chr14:76059055
|
A | G | 3 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0380 | 3 | HG02055.hp1 HG02280.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.249-272A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 4/8 | chr14 | 76059055 | ||||||
chr14:76059163
|
G | A | 4 | a0001c0001t0001g0088a0001c0001t0001g0120a0001c0001t0001g0133others(1): Show | 4 | HG02040.hp1 HG02683.hp1 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.249-164G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 4/8 | chr14 | 76059163 | ||||||
chr14:76059172
|
A | C | 117 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0017others(114): Show | 119 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(116): Show |
intron_variant | MODIFIER | c.249-155A>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 4/8 | chr14 | 76059172 | ||||||
chr14:76059210
|
A | G | 117 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0017others(114): Show | 119 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(116): Show |
intron_variant | MODIFIER | c.249-117A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 4/8 | chr14 | 76059210 | ||||||
chr14:76059277
|
C | T | 2 | a0001c0001t0001g0115a0001c0001t0001g0380 | 2 | HG02055.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.249-50C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 4/8 | chr14 | 76059277 | ||||||
chr14:76059278
|
G | A | 1 | a0001c0001t0001g0286 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.249-49G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 4/8 | chr14 | 76059278 | ||||||
chr14:76059719
|
A | G | 1 | a0001c0001t0001g0177 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.295+346A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76059719 | ||||||
chr14:76059765
|
T | A | 8 | a0001c0001t0001g0074a0001c0001t0001g0092a0001c0001t0001g0093others(5): Show | 8 | HG02109.hp2 HG02572.hp1 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.295+392T>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76059765 | ||||||
chr14:76059770
|
A | G | 70 | a0001c0001t0001g0010a0001c0001t0001g0017a0001c0001t0001g0063others(67): Show | 71 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(68): Show |
intron_variant | MODIFIER | c.295+397A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76059770 | ||||||
chr14:76060030
|
C | T | 9 | a0001c0001t0001g0009a0001c0001t0001g0105a0001c0001t0001g0251others(6): Show | 10 | HG01884.hp1 HG01891.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.295+657C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76060030 | ||||||
chr14:76060033
|
A | G | 1 | a0001c0001t0001g0363 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.295+660A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76060033 | ||||||
chr14:76060042
|
A | G | 12 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0107others(9): Show | 12 | HG00408.hp2 HG00673.hp1 HG01361.hp2 others(9): Show |
intron_variant | MODIFIER | c.295+669A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76060042 | ||||||
chr14:76060046
|
A | T | 1 | a0001c0001t0001g0163 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.295+673A>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76060046 | ||||||
chr14:76060179
|
A | T | 1 | a0001c0001t0001g0163 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.295+806A>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76060179 | ||||||
chr14:76060313
|
G | A | 1 | a0001c0001t0001g0016 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.295+940G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76060313 | ||||||
chr14:76060428
|
A | G | 144 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0010others(141): Show | 147 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(144): Show |
intron_variant | MODIFIER | c.295+1055A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76060428 | ||||||
chr14:76060534
|
C | CT | 95 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(92): Show | 98 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(95): Show |
intron_variant | MODIFIER | c.295+1171dupT | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr14 | 76060534 | |||||
chr14:76060825
|
C | T | 1 | a0001c0001t0001g0373 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.295+1452C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76060825 | ||||||
chr14:76060825
|
CCTTT | C | 9 | a0001c0001t0001g0074a0001c0001t0001g0092a0001c0001t0001g0093others(6): Show | 9 | HG02109.hp2 HG02572.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.295+1456_295+1459d others(6): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr14 | 76060825 | |||||
chr14:76060828
|
T | C | 117 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0017others(114): Show | 119 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(116): Show |
intron_variant | MODIFIER | c.295+1455T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76060828 | ||||||
chr14:76060829
|
T | C | 117 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0017others(114): Show | 119 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(116): Show |
intron_variant | MODIFIER | c.295+1456T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76060829 | ||||||
chr14:76060829
|
T | TCTTC | 23 | a0001c0001t0001g0101a0001c0001t0001g0131a0001c0001t0001g0137others(20): Show | 23 | HG00408.hp1 HG00673.hp2 HG02027.hp2 others(20): Show |
intron_variant | MODIFIER | c.295+1485_295+1488d others(6): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr14 | 76060829 | |||||
chr14:76060829
|
TCTTC | T | 155 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(152): Show | 159 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(156): Show |
intron_variant | MODIFIER | c.295+1485_295+1488d others(6): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr14 | 76060829 | |||||
chr14:76060832
|
T | C | 126 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0017others(123): Show | 128 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(125): Show |
intron_variant | MODIFIER | c.295+1459T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76060832 | ||||||
chr14:76060837
|
C | T | 111 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0017others(108): Show | 113 | HG00423.hp2 HG00438.hp2 HG00642.hp2 others(110): Show |
intron_variant | MODIFIER | c.295+1464C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76060837 | ||||||
chr14:76060857
|
C | T | 125 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0017others(122): Show | 127 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(124): Show |
intron_variant | MODIFIER | c.295+1484C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76060857 | ||||||
chr14:76060864
|
T | C | 1 | a0001c0001t0001g0373 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.295+1491T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76060864 | ||||||
chr14:76060881
|
T | TCTCCC | 126 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0017others(123): Show | 128 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(125): Show |
intron_variant | MODIFIER | c.295+1517_295+1521d others(7): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr14 | 76060881 | |||||
chr14:76061019
|
A | G | 1 | a0001c0001t0001g0016 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.295+1646A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76061019 | ||||||
chr14:76061063
|
G | A | 5 | a0001c0001t0001g0368a0001c0001t0001g0369a0001c0001t0001g0370others(2): Show | 5 | HG01109.hp2 HG02486.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.295+1690G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76061063 | ||||||
chr14:76061072
|
G | T | 115 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0017others(112): Show | 117 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(114): Show |
intron_variant | MODIFIER | c.295+1699G>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76061072 | ||||||
chr14:76061105
|
T | C | 3 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0380 | 3 | HG02055.hp1 HG02280.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.295+1732T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76061105 | ||||||
chr14:76061148
|
C | T | 1 | a0001c0001t0001g0271 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.295+1775C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76061148 | ||||||
chr14:76061271
|
C | T | 1 | a0001c0001t0001g0056 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.295+1898C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76061271 | ||||||
chr14:76061306
|
C | A | 126 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0017others(123): Show | 128 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(125): Show |
intron_variant | MODIFIER | c.295+1933C>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76061306 | ||||||
chr14:76061313
|
G | A | 12 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0107others(9): Show | 12 | HG00408.hp2 HG00673.hp1 HG01361.hp2 others(9): Show |
intron_variant | MODIFIER | c.295+1940G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76061313 | ||||||
chr14:76061459
|
A | G | 1 | a0001c0001t0001g0373 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.295+2086A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76061459 | ||||||
chr14:76061517
|
A | C | 1 | a0001c0001t0001g0227 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.295+2144A>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76061517 | ||||||
chr14:76061641
|
T | C | 1 | a0001c0001t0001g0180 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.295+2268T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76061641 | ||||||
chr14:76061943
|
T | C | 9 | a0001c0001t0001g0074a0001c0001t0001g0092a0001c0001t0001g0093others(6): Show | 9 | HG02109.hp2 HG02572.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.295+2570T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76061943 | ||||||
chr14:76062008
|
T | C | 1 | a0001c0001t0001g0214 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.295+2635T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76062008 | ||||||
chr14:76062021
|
A | T | 3 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0380 | 3 | HG02055.hp1 HG02280.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.295+2648A>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76062021 | ||||||
chr14:76062089
|
T | G | 331 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(328): Show | 344 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(341): Show |
intron_variant | MODIFIER | c.295+2716T>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76062089 | ||||||
chr14:76062216
|
G | A | 9 | a0001c0001t0001g0074a0001c0001t0001g0092a0001c0001t0001g0093others(6): Show | 9 | HG02109.hp2 HG02572.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.295+2843G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76062216 | ||||||
chr14:76062227
|
C | T | 94 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(91): Show | 97 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(94): Show |
intron_variant | MODIFIER | c.295+2854C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76062227 | ||||||
chr14:76062237
|
A | AT | 6 | a0001c0001t0001g0106a0001c0001t0001g0283a0001c0001t0001g0291others(3): Show | 6 | HG01433.hp1 HG01496.hp1 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.295+2870dupT | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr14 | 76062237 | |||||
chr14:76062312
|
C | T | 91 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(88): Show | 94 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(91): Show |
intron_variant | MODIFIER | c.295+2939C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76062312 | ||||||
chr14:76062333
|
G | A | 11 | a0001c0001t0001g0046a0001c0001t0001g0141a0001c0001t0001g0144others(8): Show | 11 | HG01106.hp2 HG01175.hp1 HG01928.hp1 others(8): Show |
intron_variant | MODIFIER | c.295+2960G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76062333 | ||||||
chr14:76062365
|
C | T | 1 | a0001c0001t0001g0116 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.295+2992C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76062365 | ||||||
chr14:76062371
|
G | A | 1 | a0001c0001t0001g0304 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.295+2998G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76062371 | ||||||
chr14:76062489
|
A | G | 6 | a0001c0001t0001g0065a0001c0001t0001g0066a0001c0001t0001g0246others(3): Show | 6 | HG02258.hp1 HG02622.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.295+3116A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76062489 | ||||||
chr14:76062590
|
G | A | 7 | a0001c0001t0001g0013a0001c0001t0001g0065a0001c0001t0001g0066others(4): Show | 7 | HG02258.hp1 HG02622.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.295+3217G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76062590 | ||||||
chr14:76062611
|
A | G | 1 | a0001c0001t0001g0016 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.295+3238A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76062611 | ||||||
chr14:76062637
|
TCAGGCGC others(10551): Show |
T | 1 | a0001c0001t0001g0016 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.295+3269_296-9096d others(2): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr14 | 76062637 | |||||
chr14:76062642
|
C | T | 1 | a0001c0001t0001g0036 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.295+3269C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76062642 | ||||||
chr14:76062710
|
A | AG | 379 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(376): Show | 394 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(391): Show |
intron_variant | MODIFIER | c.295+3337_295+3338i others(3): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76062710 | ||||||
chr14:76062743
|
G | A | 1 | a0001c0004t0001g0231 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.295+3370G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76062743 | ||||||
chr14:76062747
|
C | G | 1 | a0001c0001t0001g0264 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.295+3374C>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76062747 | ||||||
chr14:76062809
|
C | A | 1 | a0001c0001t0001g0264 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.295+3436C>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76062809 | ||||||
chr14:76062917
|
C | CA | 20 | a0001c0001t0001g0101a0001c0001t0001g0308a0001c0001t0001g0317others(17): Show | 20 | HG00408.hp1 HG00673.hp2 HG02027.hp2 others(17): Show |
intron_variant | MODIFIER | c.295+3568dupA | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr14 | 76062917 | |||||
chr14:76062917
|
C | CAAAAAAA others(7): Show |
1 | a0001c0001t0001g0077 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.295+3555_295+3568d others(16): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr14 | 76062917 | |||||
chr14:76062917
|
C | CAAAAAAA others(8): Show |
2 | a0001c0001t0001g0036a0001c0001t0001g0227 | 2 | HG01167.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.295+3554_295+3568d others(17): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr14 | 76062917 | |||||
chr14:76062917
|
C | CAAAAAAA others(9): Show |
3 | a0001c0001t0001g0065a0001c0001t0001g0246a0001c0001t0001g0247 | 3 | HG02258.hp1 HG02622.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.295+3553_295+3568d others(18): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr14 | 76062917 | |||||
chr14:76062917
|
C | CAAAAAAA others(11): Show |
1 | a0001c0001t0001g0248 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.295+3551_295+3568d others(20): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr14 | 76062917 | |||||
chr14:76062917
|
C | CAAAAAAA others(15): Show |
1 | a0001c0001t0001g0066 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.295+3547_295+3568d others(24): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr14 | 76062917 | |||||
chr14:76062917
|
CA | C | 17 | a0001c0001t0001g0018a0001c0001t0001g0074a0001c0001t0001g0092others(14): Show | 17 | HG00597.hp1 HG00642.hp1 HG01981.hp2 others(14): Show |
intron_variant | MODIFIER | c.295+3568delA | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr14 | 76062917 | |||||
chr14:76062917
|
CAA | C | 82 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(79): Show | 85 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.295+3567_295+3568d others(4): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr14 | 76062917 | |||||
chr14:76062917
|
CAAAA | C | 53 | a0001c0001t0001g0004a0001c0001t0001g0013a0001c0001t0001g0022others(50): Show | 54 | HG00099.hp1 HG00597.hp2 HG00609.hp2 others(51): Show |
intron_variant | MODIFIER | c.295+3565_295+3568d others(6): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr14 | 76062917 | |||||
chr14:76062917
|
CAAAAAAA others(5): Show |
C | 1 | a0001c0001t0001g0140 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.295+3557_295+3568d others(14): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr14 | 76062917 | |||||
chr14:76062936
|
A | AAAAG | 7 | a0001c0001t0001g0009a0001c0001t0001g0105a0001c0001t0001g0251others(4): Show | 8 | HG01891.hp2 HG02615.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.295+3566_295+3567i others(6): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr14 | 76062936 | |||||
chr14:76062938
|
A | AAAAAAAG others(7): Show |
13 | a0001c0001t0001g0017a0001c0001t0001g0030a0001c0001t0001g0049others(10): Show | 13 | HG00642.hp2 HG01192.hp2 HG01993.hp2 others(10): Show |
intron_variant | MODIFIER | c.295+3568_295+3569i others(16): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr14 | 76062938 | |||||
chr14:76062938
|
A | AAAAAAGA others(6): Show |
94 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0023others(91): Show | 96 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.295+3568_295+3569i others(15): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr14 | 76062938 | |||||
chr14:76062938
|
A | AAAAAGAA others(5): Show |
9 | a0001c0001t0001g0020a0001c0001t0001g0026a0001c0001t0001g0027others(6): Show | 9 | HG01167.hp2 HG01256.hp1 HG01258.hp1 others(6): Show |
intron_variant | MODIFIER | c.295+3568_295+3569i others(14): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr14 | 76062938 | |||||
chr14:76062947
|
T | G | 3 | a0001c0001t0001g0019a0001c0001t0001g0152a0001c0001t0001g0153 | 3 | HG01952.hp2 HG02004.hp2 HG02273.hp2 |
intron_variant | MODIFIER | c.295+3574T>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76062947 | ||||||
chr14:76062948
|
A | G | 294 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(291): Show | 301 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(298): Show |
intron_variant | MODIFIER | c.295+3575A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76062948 | ||||||
chr14:76062954
|
A | G | 1 | a0001c0001t0001g0013 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.295+3581A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76062954 | ||||||
chr14:76062991
|
T | C | 1 | a0001c0001t0001g0330 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.295+3618T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76062991 | ||||||
chr14:76063093
|
T | C | 1 | a0001c0001t0001g0256 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.295+3720T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76063093 | ||||||
chr14:76063110
|
A | G | 1 | a0001c0001t0001g0348 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.295+3737A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76063110 | ||||||
chr14:76063234
|
C | T | 3 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0380 | 3 | HG02055.hp1 HG02280.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.295+3861C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76063234 | ||||||
chr14:76063340
|
G | T | 2 | a0001c0001t0001g0311a0001c0001t0001g0312 | 2 | NA18747.hp2 NA19055.hp1 |
intron_variant | MODIFIER | c.295+3967G>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76063340 | ||||||
chr14:76063597
|
A | G | 127 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0017others(124): Show | 129 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(126): Show |
intron_variant | MODIFIER | c.295+4224A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76063597 | ||||||
chr14:76063602
|
C | T | 25 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(22): Show | 27 | HG00423.hp1 HG00438.hp1 HG00609.hp1 others(24): Show |
intron_variant | MODIFIER | c.295+4229C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76063602 | ||||||
chr14:76063953
|
G | A | 1 | a0001c0001t0001g0306 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.295+4580G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76063953 | ||||||
chr14:76064079
|
C | CT | 9 | a0001c0001t0001g0074a0001c0001t0001g0092a0001c0001t0001g0093others(6): Show | 9 | HG02109.hp2 HG02572.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.295+4707dupT | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr14 | 76064079 | |||||
chr14:76064295
|
A | T | 15 | a0001c0001t0001g0215a0001c0001t0001g0216a0001c0001t0001g0217others(12): Show | 15 | HG00099.hp2 HG00280.hp2 HG00733.hp2 others(12): Show |
intron_variant | MODIFIER | c.295+4922A>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76064295 | ||||||
chr14:76064332
|
C | T | 9 | a0001c0001t0001g0074a0001c0001t0001g0092a0001c0001t0001g0093others(6): Show | 9 | HG02109.hp2 HG02572.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.295+4959C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76064332 | ||||||
chr14:76064360
|
C | T | 33 | a0001c0001t0001g0020a0001c0001t0001g0023a0001c0001t0001g0024others(30): Show | 33 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(30): Show |
intron_variant | MODIFIER | c.295+4987C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76064360 | ||||||
chr14:76064476
|
C | T | 2 | a0001c0001t0001g0103a0001c0001t0001g0227 | 2 | HG01167.hp1 NA18997.hp1 |
intron_variant | MODIFIER | c.295+5103C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76064476 | ||||||
chr14:76064567
|
G | A | 115 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0017others(112): Show | 117 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(114): Show |
intron_variant | MODIFIER | c.295+5194G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76064567 | ||||||
chr14:76064569
|
G | A | 3 | a0001c0001t0001g0108a0001c0001t0001g0109a0001c0001t0001g0289 | 3 | HG01516.hp2 HG01517.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.295+5196G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76064569 | ||||||
chr14:76064578
|
G | T | 115 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0017others(112): Show | 117 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(114): Show |
intron_variant | MODIFIER | c.295+5205G>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76064578 | ||||||
chr14:76064583
|
A | G | 33 | a0001c0001t0001g0020a0001c0001t0001g0023a0001c0001t0001g0024others(30): Show | 33 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(30): Show |
intron_variant | MODIFIER | c.295+5210A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76064583 | ||||||
chr14:76064651
|
C | T | 1 | a0001c0001t0001g0062 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.295+5278C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76064651 | ||||||
chr14:76064797
|
C | T | 28 | a0001c0001t0001g0022a0001c0001t0001g0122a0001c0001t0001g0201others(25): Show | 28 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(25): Show |
intron_variant | MODIFIER | c.295+5424C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76064797 | ||||||
chr14:76064859
|
C | G | 1 | a0001c0001t0001g0011 | 2 | HG01074.hp2 HG01099.hp2 |
intron_variant | MODIFIER | c.295+5486C>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76064859 | ||||||
chr14:76064920
|
T | C | 81 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0017others(78): Show | 83 | HG00438.hp2 HG00642.hp2 HG01070.hp1 others(80): Show |
intron_variant | MODIFIER | c.295+5547T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76064920 | ||||||
chr14:76065090
|
C | G | 126 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0017others(123): Show | 128 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(125): Show |
intron_variant | MODIFIER | c.295+5717C>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76065090 | ||||||
chr14:76065106
|
C | T | 1 | a0001c0001t0001g0373 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.295+5733C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76065106 | ||||||
chr14:76065122
|
T | C | 2 | a0001c0001t0001g0066a0001c0001t0001g0256 | 2 | NA19043.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.295+5749T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76065122 | ||||||
chr14:76065130
|
T | C | 27 | a0001c0001t0001g0201a0001c0001t0001g0202a0001c0001t0001g0203others(24): Show | 27 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(24): Show |
intron_variant | MODIFIER | c.295+5757T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76065130 | ||||||
chr14:76065166
|
A | T | 1 | a0001c0001t0001g0256 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.295+5793A>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76065166 | ||||||
chr14:76065378
|
G | T | 3 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0380 | 3 | HG02055.hp1 HG02280.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.295+6005G>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76065378 | ||||||
chr14:76065479
|
G | A | 115 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0017others(112): Show | 117 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(114): Show |
intron_variant | MODIFIER | c.295+6106G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76065479 | ||||||
chr14:76065568
|
C | T | 2 | a0001c0001t0001g0221a0001c0001t0001g0232 | 2 | HG00099.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.295+6195C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76065568 | ||||||
chr14:76065570
|
A | G | 68 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0021others(65): Show | 70 | HG00099.hp1 HG00408.hp2 HG00597.hp2 others(67): Show |
intron_variant | MODIFIER | c.295+6197A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76065570 | ||||||
chr14:76065715
|
G | C | 9 | a0001c0001t0001g0074a0001c0001t0001g0092a0001c0001t0001g0093others(6): Show | 9 | HG02109.hp2 HG02572.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.295+6342G>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76065715 | ||||||
chr14:76065872
|
G | A | 1 | a0001c0001t0001g0227 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.295+6499G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76065872 | ||||||
chr14:76065880
|
G | T | 1 | a0001c0001t0001g0060 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.295+6507G>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76065880 | ||||||
chr14:76065998
|
C | T | 1 | a0001c0001t0001g0344 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.295+6625C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76065998 | ||||||
chr14:76066045
|
C | G | 1 | a0001c0001t0001g0373 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.295+6672C>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76066045 | ||||||
chr14:76066084
|
C | G | 79 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0017others(76): Show | 81 | HG00438.hp2 HG00642.hp2 HG01070.hp1 others(78): Show |
intron_variant | MODIFIER | c.295+6711C>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76066084 | ||||||
chr14:76066350
|
G | A | 80 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0017others(77): Show | 82 | HG00438.hp2 HG00642.hp2 HG01070.hp1 others(79): Show |
intron_variant | MODIFIER | c.295+6977G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76066350 | ||||||
chr14:76066536
|
C | T | 57 | a0001c0001t0001g0004a0001c0001t0001g0021a0001c0001t0001g0022others(54): Show | 58 | HG00099.hp1 HG00408.hp2 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.295+7163C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76066536 | ||||||
chr14:76066608
|
C | T | 149 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(146): Show | 153 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(150): Show |
intron_variant | MODIFIER | c.295+7235C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76066608 | ||||||
chr14:76066697
|
T | G | 1 | a0001c0001t0001g0287 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.295+7324T>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76066697 | ||||||
chr14:76066702
|
A | G | 3 | a0001c0001t0001g0220a0001c0001t0001g0225a0001c0001t0001g0233 | 3 | HG02165.hp1 NA18978.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.295+7329A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76066702 | ||||||
chr14:76066768
|
A | C | 7 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0368others(4): Show | 7 | HG01109.hp2 HG02486.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.295+7395A>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76066768 | ||||||
chr14:76066785
|
G | A | 3 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0380 | 3 | HG02055.hp1 HG02280.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.295+7412G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76066785 | ||||||
chr14:76067112
|
G | A | 39 | a0001c0001t0001g0004a0001c0001t0001g0021a0001c0001t0001g0022others(36): Show | 40 | HG00099.hp1 HG00597.hp2 HG00609.hp2 others(37): Show |
intron_variant | MODIFIER | c.295+7739G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76067112 | ||||||
chr14:76067288
|
G | A | 1 | a0001c0001t0001g0131 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.295+7915G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76067288 | ||||||
chr14:76067419
|
A | T | 1 | a0001c0001t0001g0373 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.295+8046A>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76067419 | ||||||
chr14:76067427
|
G | A | 1 | a0001c0001t0001g0290 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.295+8054G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76067427 | ||||||
chr14:76067527
|
A | G | 2 | a0001c0001t0001g0023a0001c0001t0001g0059 | 2 | HG01243.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.295+8154A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76067527 | ||||||
chr14:76067568
|
T | C | 1 | a0001c0001t0001g0028 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.295+8195T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76067568 | ||||||
chr14:76067579
|
C | CA | 44 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0025others(41): Show | 45 | HG01074.hp1 HG01081.hp1 HG01243.hp2 others(42): Show |
intron_variant | MODIFIER | c.295+8219dupA | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr14 | 76067579 | |||||
chr14:76067579
|
C | CAA | 24 | a0001c0001t0001g0202a0001c0001t0001g0203a0001c0001t0001g0205others(21): Show | 24 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(21): Show |
intron_variant | MODIFIER | c.295+8218_295+8219d others(4): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr14 | 76067579 | |||||
chr14:76067579
|
CA | C | 6 | a0001c0001t0001g0020a0001c0001t0001g0022a0001c0001t0001g0116others(3): Show | 6 | HG01070.hp1 HG02451.hp2 NA18955.hp2 others(3): Show |
intron_variant | MODIFIER | c.295+8219delA | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr14 | 76067579 | |||||
chr14:76067603
|
G | T | 9 | a0001c0001t0001g0074a0001c0001t0001g0092a0001c0001t0001g0093others(6): Show | 9 | HG02109.hp2 HG02572.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.295+8230G>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76067603 | ||||||
chr14:76067622
|
T | C | 1 | a0001c0001t0001g0020 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.295+8249T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76067622 | ||||||
chr14:76067765
|
C | T | 126 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0017others(123): Show | 128 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(125): Show |
intron_variant | MODIFIER | c.295+8392C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76067765 | ||||||
chr14:76067773
|
C | T | 17 | a0001c0001t0001g0020a0001c0001t0001g0023a0001c0001t0001g0024others(14): Show | 17 | HG01243.hp1 HG01884.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.295+8400C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76067773 | ||||||
chr14:76067810
|
T | C | 126 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0017others(123): Show | 128 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(125): Show |
intron_variant | MODIFIER | c.295+8437T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76067810 | ||||||
chr14:76068225
|
A | G | 9 | a0001c0001t0001g0074a0001c0001t0001g0092a0001c0001t0001g0093others(6): Show | 9 | HG02109.hp2 HG02572.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.295+8852A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76068225 | ||||||
chr14:76068252
|
A | C | 1 | a0001c0001t0001g0373 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.295+8879A>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76068252 | ||||||
chr14:76068344
|
C | T | 1 | a0001c0001t0001g0078 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.295+8971C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76068344 | ||||||
chr14:76068634
|
T | C | 1 | a0001c0001t0001g0013 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.295+9261T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76068634 | ||||||
chr14:76068804
|
G | A | 80 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0017others(77): Show | 82 | HG00438.hp2 HG00642.hp2 HG01070.hp1 others(79): Show |
intron_variant | MODIFIER | c.295+9431G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76068804 | ||||||
chr14:76068852
|
A | G | 1 | a0001c0001t0001g0369 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.295+9479A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76068852 | ||||||
chr14:76068893
|
A | G | 2 | a0001c0001t0001g0186a0001c0001t0001g0197 | 2 | NA18992.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.295+9520A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76068893 | ||||||
chr14:76068896
|
G | T | 1 | a0001c0001t0001g0062 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.295+9523G>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76068896 | ||||||
chr14:76068989
|
A | G | 9 | a0001c0001t0001g0074a0001c0001t0001g0092a0001c0001t0001g0093others(6): Show | 9 | HG02109.hp2 HG02572.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.295+9616A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76068989 | ||||||
chr14:76069125
|
A | C | 1 | a0001c0001t0001g0181 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.295+9752A>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76069125 | ||||||
chr14:76069307
|
G | A | 2 | a0001c0001t0001g0114a0001c0001t0001g0380 | 2 | HG02055.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.295+9934G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76069307 | ||||||
chr14:76069318
|
C | G | 2 | a0001c0001t0001g0146a0001c0001t0001g0154 | 2 | HG02056.hp1 HG02132.hp2 |
intron_variant | MODIFIER | c.295+9945C>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76069318 | ||||||
chr14:76069464
|
A | G | 2 | a0001c0001t0001g0333a0001c0001t0001g0354 | 2 | NA18981.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.295+10091A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76069464 | ||||||
chr14:76069513
|
A | G | 1 | a0001c0001t0001g0256 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.295+10140A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76069513 | ||||||
chr14:76069742
|
G | A | 1 | a0001c0001t0001g0373 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.295+10369G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76069742 | ||||||
chr14:76069826
|
C | T | 2 | a0001c0001t0001g0333a0001c0001t0001g0354 | 2 | NA18981.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.295+10453C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76069826 | ||||||
chr14:76069899
|
C | T | 8 | a0001c0001t0001g0074a0001c0001t0001g0092a0001c0001t0001g0093others(5): Show | 8 | HG02109.hp2 HG02572.hp1 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.295+10526C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76069899 | ||||||
chr14:76070502
|
G | A | 16 | a0001c0001t0001g0035a0001c0001t0001g0037a0001c0001t0001g0038others(13): Show | 16 | HG01928.hp2 HG01943.hp1 HG01975.hp2 others(13): Show |
intron_variant | MODIFIER | c.295+11129G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76070502 | ||||||
chr14:76070874
|
C | T | 1 | a0001c0001t0001g0290 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.296-11421C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76070874 | ||||||
chr14:76070918
|
T | C | 126 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0017others(123): Show | 128 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(125): Show |
intron_variant | MODIFIER | c.296-11377T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76070918 | ||||||
chr14:76070950
|
T | G | 1 | a0001c0001t0001g0360 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.296-11345T>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76070950 | ||||||
chr14:76071043
|
G | A | 293 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(290): Show | 300 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(297): Show |
intron_variant | MODIFIER | c.296-11252G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76071043 | ||||||
chr14:76071282
|
G | A | 2 | a0001c0001t0001g0156a0001c0001t0001g0162 | 2 | NA18939.hp1 NA18974.hp1 |
intron_variant | MODIFIER | c.296-11013G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76071282 | ||||||
chr14:76071478
|
G | A | 9 | a0001c0001t0001g0074a0001c0001t0001g0092a0001c0001t0001g0093others(6): Show | 9 | HG02109.hp2 HG02572.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.296-10817G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76071478 | ||||||
chr14:76071534
|
A | G | 1 | a0001c0001t0001g0102 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.296-10761A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76071534 | ||||||
chr14:76071591
|
G | T | 1 | a0001c0001t0001g0135 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.296-10704G>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76071591 | ||||||
chr14:76071841
|
G | A | 1 | a0001c0001t0001g0227 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.296-10454G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76071841 | ||||||
chr14:76071891
|
C | T | 1 | a0001c0001t0001g0025 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.296-10404C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76071891 | ||||||
chr14:76071969
|
C | A | 126 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0017others(123): Show | 128 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(125): Show |
intron_variant | MODIFIER | c.296-10326C>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76071969 | ||||||
chr14:76072439
|
A | C | 3 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0380 | 3 | HG02055.hp1 HG02280.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.296-9856A>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76072439 | ||||||
chr14:76072700
|
T | C | 126 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0017others(123): Show | 128 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(125): Show |
intron_variant | MODIFIER | c.296-9595T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76072700 | ||||||
chr14:76072739
|
A | C | 2 | a0001c0001t0001g0012a0001c0001t0001g0326 | 3 | HG03491.hp2 HG03492.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.296-9556A>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76072739 | ||||||
chr14:76072832
|
G | A | 15 | a0001c0001t0001g0020a0001c0001t0001g0023a0001c0001t0001g0024others(12): Show | 15 | HG01243.hp1 HG01884.hp2 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.296-9463G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76072832 | ||||||
chr14:76072923
|
A | G | 3 | a0001c0001t0001g0159a0001c0001t0001g0160a0001c0001t0001g0161 | 3 | HG01928.hp1 HG01993.hp1 HG02148.hp1 |
intron_variant | MODIFIER | c.296-9372A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76072923 | ||||||
chr14:76072978
|
G | A | 11 | a0001c0001t0001g0046a0001c0001t0001g0141a0001c0001t0001g0144others(8): Show | 11 | HG01106.hp2 HG01175.hp1 HG01928.hp1 others(8): Show |
intron_variant | MODIFIER | c.296-9317G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76072978 | ||||||
chr14:76072992
|
C | G | 107 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0017others(104): Show | 109 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.296-9303C>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76072992 | ||||||
chr14:76073222
|
A | G | 27 | a0001c0001t0001g0201a0001c0001t0001g0202a0001c0001t0001g0203others(24): Show | 27 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(24): Show |
intron_variant | MODIFIER | c.296-9073A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76073222 | ||||||
chr14:76073251
|
G | A | 2 | a0001c0001t0001g0034a0001c0001t0001g0132 | 2 | NA19240.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.296-9044G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76073251 | ||||||
chr14:76073266
|
G | C | 1 | a0001c0001t0001g0284 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.296-9029G>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76073266 | ||||||
chr14:76073490
|
C | T | 1 | a0001c0001t0001g0373 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.296-8805C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76073490 | ||||||
chr14:76073577
|
GTGTGTGT others(21): Show |
G | 1 | a0001c0001t0001g0309 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.296-8707_296-8680d others(30): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr14 | 76073577 | |||||
chr14:76073607
|
G | C | 1 | a0001c0001t0001g0091 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.296-8688G>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76073607 | ||||||
chr14:76073814
|
C | T | 1 | a0001c0001t0001g0373 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.296-8481C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76073814 | ||||||
chr14:76073834
|
T | C | 123 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0017others(120): Show | 125 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(122): Show |
intron_variant | MODIFIER | c.296-8461T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76073834 | ||||||
chr14:76073866
|
C | T | 125 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0017others(122): Show | 127 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(124): Show |
intron_variant | MODIFIER | c.296-8429C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76073866 | ||||||
chr14:76073930
|
C | T | 1 | a0001c0001t0001g0307 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.296-8365C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76073930 | ||||||
chr14:76073937
|
G | A | 1 | a0001c0001t0001g0366 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.296-8358G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76073937 | ||||||
chr14:76074021
|
G | T | 1 | a0001c0001t0001g0114 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.296-8274G>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76074021 | ||||||
chr14:76074246
|
T | C | 27 | a0001c0001t0001g0201a0001c0001t0001g0202a0001c0001t0001g0203others(24): Show | 27 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(24): Show |
intron_variant | MODIFIER | c.296-8049T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76074246 | ||||||
chr14:76074255
|
T | C | 1 | a0001c0001t0001g0015 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.296-8040T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76074255 | ||||||
chr14:76074267
|
G | A | 1 | a0001c0001t0001g0013 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.296-8028G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76074267 | ||||||
chr14:76074339
|
T | G | 125 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0017others(122): Show | 127 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(124): Show |
intron_variant | MODIFIER | c.296-7956T>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76074339 | ||||||
chr14:76074405
|
G | GA | 12 | a0001c0001t0001g0074a0001c0001t0001g0092a0001c0001t0001g0093others(9): Show | 12 | HG02055.hp1 HG02109.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.296-7889dupA | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr14 | 76074405 | |||||
chr14:76074576
|
G | A | 1 | a0001c0001t0001g0104 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.296-7719G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76074576 | ||||||
chr14:76074578
|
T | G | 125 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0017others(122): Show | 127 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(124): Show |
intron_variant | MODIFIER | c.296-7717T>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76074578 | ||||||
chr14:76074618
|
T | C | 6 | a0001c0001t0001g0020a0001c0001t0001g0023a0001c0001t0001g0024others(3): Show | 6 | HG01243.hp1 HG01884.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.296-7677T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76074618 | ||||||
chr14:76074808
|
C | T | 6 | a0001c0001t0001g0020a0001c0001t0001g0023a0001c0001t0001g0024others(3): Show | 6 | HG01243.hp1 HG01884.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.296-7487C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76074808 | ||||||
chr14:76074809
|
C | T | 2 | a0001c0001t0001g0375a0001c0001t0001g0376 | 2 | HG02040.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.296-7486C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76074809 | ||||||
chr14:76074823
|
C | T | 1 | a0001c0001t0001g0227 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.296-7472C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76074823 | ||||||
chr14:76074839
|
C | G | 1 | a0001c0001t0001g0251 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.296-7456C>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76074839 | ||||||
chr14:76075012
|
G | C | 1 | a0001c0001t0001g0373 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.296-7283G>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76075012 | ||||||
chr14:76075030
|
G | A | 1 | a0001c0001t0001g0055 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.296-7265G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76075030 | ||||||
chr14:76075329
|
T | C | 126 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0017others(123): Show | 128 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(125): Show |
intron_variant | MODIFIER | c.296-6966T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76075329 | ||||||
chr14:76075378
|
CA | C | 6 | a0001c0001t0001g0020a0001c0001t0001g0023a0001c0001t0001g0024others(3): Show | 6 | HG01243.hp1 HG01884.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.296-6916delA | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76075378 | ||||||
chr14:76075384
|
A | G | 6 | a0001c0001t0001g0020a0001c0001t0001g0023a0001c0001t0001g0024others(3): Show | 6 | HG01243.hp1 HG01884.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.296-6911A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76075384 | ||||||
chr14:76075572
|
G | A | 2 | a0001c0001t0001g0026a0001c0001t0001g0027 | 2 | HG02559.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.296-6723G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76075572 | ||||||
chr14:76075606
|
T | C | 126 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0017others(123): Show | 128 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(125): Show |
intron_variant | MODIFIER | c.296-6689T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76075606 | ||||||
chr14:76075675
|
A | G | 1 | a0001c0001t0001g0264 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.296-6620A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76075675 | ||||||
chr14:76075680
|
A | G | 3 | a0001c0001t0001g0318a0001c0001t0001g0341a0001c0001t0001g0350 | 3 | NA18984.hp2 NA18986.hp2 NA19055.hp2 |
intron_variant | MODIFIER | c.296-6615A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76075680 | ||||||
chr14:76075695
|
C | T | 9 | a0001c0001t0001g0003a0001c0001t0001g0029a0001c0001t0001g0030others(6): Show | 10 | HG01081.hp1 HG01243.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.296-6600C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76075695 | ||||||
chr14:76075754
|
G | A | 1 | a0001c0001t0001g0314 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.296-6541G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76075754 | ||||||
chr14:76075941
|
G | C | 126 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0017others(123): Show | 128 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(125): Show |
intron_variant | MODIFIER | c.296-6354G>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76075941 | ||||||
chr14:76075962
|
C | G | 1 | a0001c0001t0001g0166 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.296-6333C>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76075962 | ||||||
chr14:76076014
|
G | A | 4 | a0001c0001t0001g0186a0001c0001t0001g0188a0001c0001t0001g0197others(1): Show | 4 | HG00438.hp1 NA18991.hp1 NA18992.hp2 others(1): Show |
intron_variant | MODIFIER | c.296-6281G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76076014 | ||||||
chr14:76076039
|
C | T | 1 | a0001c0001t0001g0013 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.296-6256C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76076039 | ||||||
chr14:76076071
|
T | C | 7 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0368others(4): Show | 7 | HG01109.hp2 HG02486.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.296-6224T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76076071 | ||||||
chr14:76076149
|
G | C | 107 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0017others(104): Show | 109 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.296-6146G>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76076149 | ||||||
chr14:76076159
|
G | A | 1 | a0001c0001t0001g0177 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.296-6136G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76076159 | ||||||
chr14:76076262
|
G | A | 126 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0017others(123): Show | 128 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(125): Show |
intron_variant | MODIFIER | c.296-6033G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76076262 | ||||||
chr14:76076507
|
AGATTTAT others(9): Show |
A | 1 | a0001c0001t0001g0166 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.296-5785_296-5770d others(18): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr14 | 76076507 | |||||
chr14:76076513
|
A | G | 107 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0017others(104): Show | 109 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.296-5782A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76076513 | ||||||
chr14:76076661
|
G | A | 70 | a0001c0001t0001g0010a0001c0001t0001g0017a0001c0001t0001g0063others(67): Show | 71 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(68): Show |
intron_variant | MODIFIER | c.296-5634G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76076661 | ||||||
chr14:76076908
|
AC | A | 4 | a0001c0001t0001g0052a0001c0001t0001g0062a0001c0001t0001g0087others(1): Show | 4 | HG02922.hp1 HG03209.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.296-5384delC | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr14 | 76076908 | |||||
chr14:76076932
|
C | A | 126 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0017others(123): Show | 128 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(125): Show |
intron_variant | MODIFIER | c.296-5363C>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76076932 | ||||||
chr14:76077013
|
A | G | 116 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0017others(113): Show | 118 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(115): Show |
intron_variant | MODIFIER | c.296-5282A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76077013 | ||||||
chr14:76077030
|
A | G | 168 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(165): Show | 173 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(170): Show |
intron_variant | MODIFIER | c.296-5265A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76077030 | ||||||
chr14:76077165
|
T | G | 7 | a0001c0001t0001g0004a0001c0001t0001g0070a0001c0001t0001g0071others(4): Show | 8 | HG00099.hp1 HG00733.hp1 HG00741.hp2 others(5): Show |
intron_variant | MODIFIER | c.296-5130T>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76077165 | ||||||
chr14:76077215
|
C | T | 9 | a0001c0001t0001g0009a0001c0001t0001g0105a0001c0001t0001g0251others(6): Show | 10 | HG01884.hp1 HG01891.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.296-5080C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76077215 | ||||||
chr14:76077219
|
G | GCT | 94 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(91): Show | 97 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(94): Show |
intron_variant | MODIFIER | c.296-5072_296-5071d others(4): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr14 | 76077219 | |||||
chr14:76077317
|
T | C | 125 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0017others(122): Show | 127 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(124): Show |
intron_variant | MODIFIER | c.296-4978T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76077317 | ||||||
chr14:76077358
|
C | T | 1 | a0001c0001t0001g0373 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.296-4937C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76077358 | ||||||
chr14:76077425
|
C | T | 1 | a0001c0001t0001g0013 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.296-4870C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76077425 | ||||||
chr14:76077556
|
G | A | 4 | a0001c0001t0001g0065a0001c0001t0001g0246a0001c0001t0001g0247others(1): Show | 4 | HG02258.hp1 HG02622.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.296-4739G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76077556 | ||||||
chr14:76077578
|
C | T | 5 | a0001c0001t0001g0368a0001c0001t0001g0369a0001c0001t0001g0370others(2): Show | 5 | HG01109.hp2 HG02486.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.296-4717C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76077578 | ||||||
chr14:76077894
|
A | G | 10 | a0001c0001t0001g0009a0001c0001t0001g0105a0001c0001t0001g0251others(7): Show | 11 | HG00673.hp2 HG01884.hp1 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.296-4401A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76077894 | ||||||
chr14:76078119
|
C | T | 302 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(299): Show | 309 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(306): Show |
intron_variant | MODIFIER | c.296-4176C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76078119 | ||||||
chr14:76078159
|
G | A | 1 | a0001c0001t0001g0013 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.296-4136G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76078159 | ||||||
chr14:76078194
|
G | A | 4 | a0001c0001t0001g0065a0001c0001t0001g0246a0001c0001t0001g0247others(1): Show | 4 | HG02258.hp1 HG02622.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.296-4101G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76078194 | ||||||
chr14:76078656
|
T | C | 1 | a0001c0001t0001g0065 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.296-3639T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76078656 | ||||||
chr14:76078732
|
C | T | 1 | a0001c0001t0001g0082 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.296-3563C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76078732 | ||||||
chr14:76078736
|
G | A | 55 | a0001c0001t0001g0004a0001c0001t0001g0021a0001c0001t0001g0022others(52): Show | 56 | HG00099.hp1 HG00408.hp2 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.296-3559G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76078736 | ||||||
chr14:76078743
|
G | A | 1 | a0001c0001t0001g0373 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.296-3552G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76078743 | ||||||
chr14:76078820
|
T | G | 126 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0017others(123): Show | 128 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(125): Show |
intron_variant | MODIFIER | c.296-3475T>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76078820 | ||||||
chr14:76078912
|
C | G | 1 | a0001c0001t0001g0055 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.296-3383C>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76078912 | ||||||
chr14:76078917
|
T | G | 43 | a0001c0001t0001g0010a0001c0001t0001g0017a0001c0001t0001g0063others(40): Show | 44 | HG00438.hp2 HG00642.hp2 HG01070.hp1 others(41): Show |
intron_variant | MODIFIER | c.296-3378T>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76078917 | ||||||
chr14:76078983
|
TTAGCATA others(4): Show |
T | 1 | a0001c0001t0001g0198 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.296-3308_296-3298d others(13): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr14 | 76078983 | |||||
chr14:76079001
|
T | C | 1 | a0001c0001t0001g0325 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.296-3294T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76079001 | ||||||
chr14:76079080
|
C | T | 1 | a0001c0001t0001g0115 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.296-3215C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76079080 | ||||||
chr14:76079149
|
A | G | 13 | a0001c0001t0001g0074a0001c0001t0001g0092a0001c0001t0001g0093others(10): Show | 13 | HG02055.hp1 HG02109.hp2 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.296-3146A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76079149 | ||||||
chr14:76079410
|
T | C | 5 | a0001c0001t0001g0035a0001c0001t0001g0037a0001c0001t0001g0039others(2): Show | 5 | NA18960.hp1 NA18963.hp1 NA18991.hp2 others(2): Show |
intron_variant | MODIFIER | c.296-2885T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76079410 | ||||||
chr14:76079520
|
T | G | 1 | a0001c0001t0001g0314 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.296-2775T>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76079520 | ||||||
chr14:76079703
|
G | A | 1 | a0001c0001t0001g0013 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.296-2592G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76079703 | ||||||
chr14:76079816
|
G | A | 167 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(164): Show | 172 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(169): Show |
intron_variant | MODIFIER | c.296-2479G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76079816 | ||||||
chr14:76079832
|
G | A | 126 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0017others(123): Show | 128 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(125): Show |
intron_variant | MODIFIER | c.296-2463G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76079832 | ||||||
chr14:76079863
|
T | G | 1 | a0001c0001t0001g0373 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.296-2432T>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76079863 | ||||||
chr14:76079947
|
G | T | 113 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0017others(110): Show | 115 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(112): Show |
intron_variant | MODIFIER | c.296-2348G>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76079947 | ||||||
chr14:76080072
|
G | A | 1 | a0001c0001t0001g0290 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.296-2223G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76080072 | ||||||
chr14:76080127
|
C | T | 1 | a0001c0001t0001g0373 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.296-2168C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76080127 | ||||||
chr14:76080208
|
C | T | 1 | a0001c0001t0001g0348 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.296-2087C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76080208 | ||||||
chr14:76080282
|
G | A | 92 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(89): Show | 95 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.296-2013G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76080282 | ||||||
chr14:76080423
|
C | T | 1 | a0001c0001t0001g0098 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.296-1872C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76080423 | ||||||
chr14:76080472
|
C | T | 9 | a0001c0001t0001g0074a0001c0001t0001g0092a0001c0001t0001g0093others(6): Show | 9 | HG02109.hp2 HG02572.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.296-1823C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76080472 | ||||||
chr14:76080593
|
C | A | 9 | a0001c0001t0001g0074a0001c0001t0001g0092a0001c0001t0001g0093others(6): Show | 9 | HG02109.hp2 HG02572.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.296-1702C>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76080593 | ||||||
chr14:76080667
|
T | C | 182 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0010others(179): Show | 185 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(182): Show |
intron_variant | MODIFIER | c.296-1628T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76080667 | ||||||
chr14:76080680
|
A | G | 3 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0380 | 3 | HG02055.hp1 HG02280.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.296-1615A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76080680 | ||||||
chr14:76080758
|
C | T | 1 | a0001c0001t0001g0195 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.296-1537C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76080758 | ||||||
chr14:76080794
|
A | G | 1 | a0001c0001t0001g0232 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.296-1501A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76080794 | ||||||
chr14:76080871
|
T | G | 169 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(166): Show | 174 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(171): Show |
intron_variant | MODIFIER | c.296-1424T>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76080871 | ||||||
chr14:76081098
|
A | T | 15 | a0001c0001t0001g0035a0001c0001t0001g0037a0001c0001t0001g0038others(12): Show | 15 | HG01928.hp2 HG01943.hp1 HG01975.hp2 others(12): Show |
intron_variant | MODIFIER | c.296-1197A>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76081098 | ||||||
chr14:76081182
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G | A | 13 | a0001c0001t0001g0005a0001c0001t0001g0046a0001c0001t0001g0141others(10): Show | 14 | HG01070.hp2 HG01106.hp2 HG01175.hp1 others(11): Show |
intron_variant | MODIFIER | c.296-1113G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76081182 | ||||||
chr14:76081198
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G | A | 9 | a0001c0001t0001g0074a0001c0001t0001g0092a0001c0001t0001g0093others(6): Show | 9 | HG02109.hp2 HG02572.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.296-1097G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76081198 | ||||||
chr14:76081219
|
G | C | 1 | a0001c0001t0001g0016 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.296-1076G>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76081219 | ||||||
chr14:76081326
|
G | A | 1 | a0001c0001t0001g0065 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.296-969G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76081326 | ||||||
chr14:76081338
|
G | T | 2 | a0001c0001t0001g0036a0001c0001t0001g0077 | 2 | HG02572.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.296-957G>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76081338 | ||||||
chr14:76081356
|
C | T | 1 | a0001c0001t0001g0373 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.296-939C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76081356 | ||||||
chr14:76081393
|
C | T | 1 | a0001c0001t0001g0373 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.296-902C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76081393 | ||||||
chr14:76081481
|
G | A | 1 | a0001c0001t0001g0256 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.296-814G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76081481 | ||||||
chr14:76081541
|
A | G | 1 | a0001c0001t0001g0015 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.296-754A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76081541 | ||||||
chr14:76081616
|
C | G | 2 | a0001c0001t0001g0014a0001c0001t0001g0015 | 2 | HG02723.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.296-679C>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76081616 | ||||||
chr14:76081619
|
C | T | 1 | a0001c0001t0001g0169 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.296-676C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76081619 | ||||||
chr14:76081624
|
A | G | 1 | a0001c0001t0001g0016 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.296-671A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76081624 | ||||||
chr14:76081675
|
A | G | 3 | a0001c0001t0001g0024a0001c0001t0001g0058a0001c0001t0001g0060 | 3 | HG02895.hp2 HG02965.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.296-620A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76081675 | ||||||
chr14:76081704
|
A | G | 22 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0074others(19): Show | 22 | HG01109.hp2 HG01516.hp2 HG01517.hp2 others(19): Show |
intron_variant | MODIFIER | c.296-591A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76081704 | ||||||
chr14:76081857
|
G | A | 16 | a0001c0001t0001g0009a0001c0001t0001g0036a0001c0001t0001g0052others(13): Show | 17 | HG01884.hp1 HG01891.hp2 HG02572.hp2 others(14): Show |
intron_variant | MODIFIER | c.296-438G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76081857 | ||||||
chr14:76081933
|
T | C | 1 | a0001c0001t0001g0281 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.296-362T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76081933 | ||||||
chr14:76081948
|
G | A | 3 | a0001c0001t0001g0246a0001c0001t0001g0247a0001c0001t0001g0248 | 3 | HG02258.hp1 HG02647.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.296-347G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76081948 | ||||||
chr14:76082021
|
G | A | 4 | a0001c0001t0001g0065a0001c0001t0001g0246a0001c0001t0001g0247others(1): Show | 4 | HG02258.hp1 HG02622.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.296-274G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76082021 | ||||||
chr14:76082039
|
C | A | 1 | a0001c0001t0001g0347 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.296-256C>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76082039 | ||||||
chr14:76082055
|
C | G | 1 | a0001c0001t0001g0374 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.296-240C>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76082055 | ||||||
chr14:76082086
|
A | C | 1 | a0001c0001t0001g0114 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.296-209A>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76082086 | ||||||
chr14:76082396
|
G | A | 12 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0107others(9): Show | 12 | HG00408.hp2 HG00673.hp1 HG01361.hp2 others(9): Show |
intron_variant | MODIFIER | c.368+29G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 6/8 | chr14 | 76082396 | ||||||
chr14:76082440
|
GGACCTT | G | 92 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(89): Show | 95 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.368+76_368+81delCC others(4): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr14 | 76082440 | |||||
chr14:76082510
|
T | C | 8 | a0001c0001t0001g0074a0001c0001t0001g0092a0001c0001t0001g0093others(5): Show | 8 | HG02109.hp2 HG02572.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.369-107T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 6/8 | chr14 | 76082510 | ||||||
chr14:76082968
|
G | A | 2 | a0001c0001t0001g0114a0001c0001t0001g0380 | 2 | HG02055.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.445-259G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 7/8 | chr14 | 76082968 | ||||||
chr14:76083011
|
G | A | 5 | a0001c0001t0001g0334a0001c0001t0001g0338a0001c0001t0001g0345others(2): Show | 5 | NA18940.hp2 NA18941.hp1 NA18957.hp2 others(2): Show |
intron_variant | MODIFIER | c.445-216G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 7/8 | chr14 | 76083011 | ||||||
chr14:76083034
|
G | A | 219 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(216): Show | 224 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(221): Show |
intron_variant | MODIFIER | c.445-193G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 7/8 | chr14 | 76083034 | ||||||
chr14:76083409
|
G | A | 92 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(89): Show | 95 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.508-49G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 8/8 | chr14 | 76083409 | ||||||
chr14:76083419
|
G | A | 8 | a0001c0001t0001g0074a0001c0001t0001g0092a0001c0001t0001g0093others(5): Show | 8 | HG02109.hp2 HG02572.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.508-39G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 8/8 | chr14 | 76083419 |