geneid | 51668 |
---|---|
ensemblid | ENSG00000081870.12 |
hgncid | 25019 |
symbol | IFT25 |
name | intraflagellar transport 25 |
refseq_nuc | NM_016126.4 |
refseq_prot | NP_057210.2 |
ensembl_nuc | ENST00000194214.10 |
ensembl_prot | ENSP00000194214.5 |
mane_status | MANE Select |
chr | chr1 |
start | 53921561 |
end | 53945699 |
strand | - |
ver | v1.2 |
region | chr1:53921561-53945699 |
region5000 | chr1:53916561-53950699 |
regionname0 | IFT25_chr1_53921561_53945699 |
regionname5000 | IFT25_chr1_53916561_53950699 |
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 | 144 | 281 | 94 | 37 | 110 | 12 | 26 | 80 | IFT25_chr1_53916561_53950699 | IFT25 | copy fasta | chr1 | 53916561 | 53950699 |
a0002 | 0/0 | 144 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | copy fasta | chr1 | 53916561 | 53950699 |
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 | 435 | 280 | 94 | 37 | 109 | 12 | 26 | IFT25_chr1_53916561_53950699 | IFT25 | copy fasta | chr1 | 53916561 | 53950699 |
c0002 | 0/0 | 435 | 1 | 0 | 1 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | copy fasta | chr1 | 53916561 | 53950699 |
c0003 | 0/0 | 435 | 1 | 0 | 0 | 1 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | copy fasta | chr1 | 53916561 | 53950699 |
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 | 251 | 276 | 89 | 37 | 110 | 12 | 26 | IFT25_chr1_53916561_53950699 | IFT25 | copy fasta | chr1 | 53916561 | 53950699 |
t0002 | 0/0 | 251 | 5 | 4 | 1 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | copy fasta | chr1 | 53916561 | 53950699 |
t0003 | 0/0 | 251 | 1 | 1 | 0 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | copy fasta | chr1 | 53916561 | 53950699 |
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 | 23 | 1 | 4 | 15 | 0 | 3 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
g0002 | 1/0 | 20 | 1 | 2 | 12 | 2 | 2 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
g0003 | 0/1 | 19 | 1 | 7 | 3 | 3 | 4 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
g0004 | 0/0 | 9 | 2 | 0 | 4 | 1 | 2 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
g0005 | 0/0 | 7 | 7 | 0 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
g0006 | 0/0 | 7 | 7 | 0 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
g0007 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
g0008 | 0/0 | 5 | 0 | 0 | 3 | 0 | 2 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
g0009 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
g0010 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
g0011 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
g0012 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
g0013 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
g0014 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
g0016 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
g0018 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
g0019 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
g0020 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
g0022 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
g0026 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
g0027 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
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 | 435 | 280 | 94 | 37 | 109 | 12 | 26 | IFT25_chr1_53916561_53950699 | IFT25 | copy fasta | chr1 | 53916561 | 53950699 |
a0001c0003 | 0/0 | 435 | 1 | 0 | 0 | 1 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | copy fasta | chr1 | 53916561 | 53950699 |
a0002c0002 | 0/0 | 435 | 1 | 0 | 1 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | copy fasta | chr1 | 53916561 | 53950699 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 685 | 274 | 89 | 36 | 109 | 12 | 26 | IFT25_chr1_53916561_53950699 | IFT25 | copy fasta | chr1 | 53916561 | 53950699 |
a0001c0001t0002 | 0/0 | 685 | 5 | 4 | 1 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | copy fasta | chr1 | 53916561 | 53950699 |
a0001c0001t0003 | 0/0 | 685 | 1 | 1 | 0 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | copy fasta | chr1 | 53916561 | 53950699 |
a0001c0003t0001 | 0/0 | 685 | 1 | 0 | 0 | 1 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | copy fasta | chr1 | 53916561 | 53950699 |
a0002c0002t0001 | 0/0 | 685 | 1 | 0 | 1 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | copy fasta | chr1 | 53916561 | 53950699 |
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 | 23 | 1 | 4 | 15 | 0 | 3 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0002 | 1/0 | 20 | 1 | 2 | 12 | 2 | 2 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0003 | 0/1 | 19 | 1 | 7 | 3 | 3 | 4 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0004 | 0/0 | 9 | 2 | 0 | 4 | 1 | 2 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0005 | 0/0 | 7 | 7 | 0 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0006 | 0/0 | 7 | 7 | 0 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0007 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0008 | 0/0 | 5 | 0 | 0 | 3 | 0 | 2 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0009 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0010 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0011 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0012 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0013 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0014 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0016 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0018 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0019 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0020 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0022 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0026 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0027 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0002g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0002g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0002g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0002g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0003g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0003t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0002c0002t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0019 | EUR | GBR | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | GBR | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0072 | EUR | GBR | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0070 | EUR | GBR | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0004 | EUR | FIN | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | FIN | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | CHS | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | CHS | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | CHS | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | CHS | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | CHS | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | CHS | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | CHS | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | CHS | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | CHS | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | CHS | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | CHS | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0086 | AMR | PUR | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0027 | AMR | PUR | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | CHS | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | CHS | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG01070 | hp2 | a0002 | c0002 | t0001 | g0064 | AMR | PUR | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0083 | AMR | PUR | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG01109 | hp1 | a0001 | c0001 | t0002 | g0153 | AMR | PUR | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0089 | AMR | PUR | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0060 | AMR | PUR | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0085 | AMR | PUR | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0122 | AMR | CLM | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | CLM | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0101 | AMR | CLM | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0062 | AMR | CLM | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0127 | AMR | CLM | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0075 | AMR | CLM | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | CLM | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0022 | EUR | IBS | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | IBS | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0003 | EUR | IBS | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0016 | EUR | IBS | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | ACB | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0041 | AFR | ACB | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0105 | AFR | ACB | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | ACB | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0058 | AMR | PEL | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | PEL | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | KHV | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | KHV | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0132 | AFR | ACB | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0102 | AFR | ACB | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | KHV | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG02074 | hp2 | a0001 | c0003 | t0001 | g0098 | EAS | KHV | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | KHV | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | KHV | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0119 | AFR | ACB | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | CDX | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0099 | AMR | PEL | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | ACB | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0138 | AFR | ACB | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PEL | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PEL | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG02572 | hp1 | a0001 | c0001 | t0003 | g0033 | AFR | GWD | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0111 | AFR | GWD | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0059 | SAS | PJL | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0079 | SAS | PJL | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0137 | AFR | GWD | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0110 | AFR | GWD | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | GWD | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0117 | AFR | GWD | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0118 | AFR | GWD | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0042 | SAS | PJL | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0108 | AFR | GWD | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0052 | AFR | GWD | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0077 | AFR | GWD | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | GWD | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0097 | SAS | PJL | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0123 | SAS | PJL | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | GWD | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0069 | AFR | GWD | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0147 | AFR | GWD | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | GWD | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0112 | AFR | GWD | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0140 | AFR | GWD | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | GWD | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | GWD | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | GWD | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0129 | AFR | GWD | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG02922 | hp1 | a0001 | c0001 | t0002 | g0032 | AFR | ESN | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | ESN | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0113 | AFR | ESN | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0126 | AFR | ESN | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | ESN | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | ESN | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0114 | AFR | ESN | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0115 | AFR | GWD | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | MSL | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | MSL | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0134 | AFR | ESN | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG03130 | hp2 | a0001 | c0001 | t0002 | g0154 | AFR | ESN | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0146 | AFR | ESN | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG03139 | hp2 | a0001 | c0001 | t0002 | g0155 | AFR | ESN | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG03195 | hp1 | a0001 | c0001 | t0002 | g0032 | AFR | ESN | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | ESN | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0068 | AFR | MSL | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0142 | AFR | MSL | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | MSL | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | MSL | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0144 | AFR | MSL | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | MSL | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | MSL | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | MSL | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0065 | SAS | PJL | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0063 | SAS | PJL | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ESN | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0125 | AFR | ESN | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0151 | AFR | GWD | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0139 | AFR | GWD | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0013 | SAS | PJL | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0053 | SAS | PJL | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0094 | SAS | PJL | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0088 | SAS | PJL | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | BEB | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0054 | SAS | BEB | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0046 | SAS | BEB | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0120 | AFR | YRI | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0124 | AFR | YRI | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | YRI | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0116 | AFR | YRI | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0135 | AFR | LWK | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0133 | AFR | LWK | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | LWK | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | LWK | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
NA19078 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
NA19078 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | YRI | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0145 | AFR | YRI | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | ASW | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0107 | AFR | ASW | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0003 | EUR | TSI | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0131 | EUR | TSI | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0121 | AFR | ACB | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0055 | AFR | ACB | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | ACB | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | ACB | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0136 | AFR | MSL | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | MSL | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0128 | AFR | USA | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | USA | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | USA | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0143 | AFR | USA | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | LWK | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | LWK | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0003 | REF | REF | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0002 | REF | REF | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:53923910
|
T | G | 1 | a0002 | 1 | HG01070.hp2 | missense_variant | MODERATE | c.312A>C | p.Glu104Asp | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 5/6 | 472/685 | 312/435 | 104/144 | chr1 | 53923910 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:53940044
|
G | A | 1 | a0001c0003 | 1 | HG02074.hp2 | synonymous_variant | LOW | c.39C>T | p.Ser13Ser | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/6 | 199/685 | 39/435 | 13/144 | chr1 | 53940044 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:53921615
|
A | G | 1 | a0001c0001t0002 | 5 | HG01109.hp1 HG02922.hp1 HG03130.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*36T>C | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 6/6 | 36 | chr1 | 53921615 | |||||
chr1:53945629
|
C | A | 1 | a0001c0001t0002 | 5 | HG01109.hp1 HG02922.hp1 HG03130.hp2 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-90G>T | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 1/6 | 5547 | chr1 | 53945629 | |||||
chr1:53945646
|
C | T | 1 | a0001c0001t0003 | 1 | HG02572.hp1 | 5_prime_UTR_variant | MODIFIER | c.-107G>A | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 1/6 | 5564 | chr1 | 53945646 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:53921772
|
A | T | 2 | a0001c0001t0001g0120a0001c0001t0001g0132 | 2 | HG02055.hp1 NA18522.hp1 |
splice_region_variant&intron_variant | LOW | c.319-5T>A | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 5/5 | chr1 | 53921772 | ||||||
chr1:53921904
|
T | C | 51 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(48): Show | 83 | HG00099.hp1 HG00280.hp1 HG00558.hp1 others(80): Show |
intron_variant | MODIFIER | c.319-137A>G | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 5/5 | chr1 | 53921904 | ||||||
chr1:53922184
|
T | C | 59 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(56): Show | 96 | HG00099.hp1 HG00280.hp1 HG00558.hp1 others(93): Show |
intron_variant | MODIFIER | c.319-417A>G | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 5/5 | chr1 | 53922184 | ||||||
chr1:53922390
|
G | A | 1 | a0001c0001t0001g0021 | 2 | NA19063.hp2 NA19078.hp1 |
intron_variant | MODIFIER | c.319-623C>T | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 5/5 | chr1 | 53922390 | ||||||
chr1:53922394
|
CA | C | 6 | a0001c0001t0001g0107a0001c0001t0001g0133a0001c0001t0001g0137others(3): Show | 6 | HG02280.hp2 HG02615.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.319-628delT | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 5/5 | chr1 | 53922394 | ||||||
chr1:53922394
|
CAA | C | 46 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(43): Show | 78 | HG00099.hp1 HG00280.hp1 HG00558.hp1 others(75): Show |
intron_variant | MODIFIER | c.319-629_319-628del others(2): Show |
IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 5/5 | chr1 | 53922394 | ||||||
chr1:53922394
|
CAAA | C | 3 | a0001c0001t0001g0011a0001c0001t0001g0111a0001c0001t0001g0112 | 6 | HG02572.hp2 HG02647.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.319-630_319-628del others(3): Show |
IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 5/5 | chr1 | 53922394 | ||||||
chr1:53922476
|
G | A | 1 | a0001c0001t0001g0081 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.319-709C>T | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 5/5 | chr1 | 53922476 | ||||||
chr1:53922634
|
A | C | 55 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(52): Show | 88 | HG00099.hp1 HG00280.hp1 HG00558.hp1 others(85): Show |
intron_variant | MODIFIER | c.319-867T>G | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 5/5 | chr1 | 53922634 | ||||||
chr1:53922852
|
G | A | 1 | a0001c0001t0001g0035 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.318+1052C>T | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 5/5 | chr1 | 53922852 | ||||||
chr1:53923163
|
A | C | 1 | a0001c0001t0001g0042 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.318+741T>G | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 5/5 | chr1 | 53923163 | ||||||
chr1:53923297
|
T | TAATA | 55 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(52): Show | 88 | HG00099.hp1 HG00280.hp1 HG00558.hp1 others(85): Show |
intron_variant | MODIFIER | c.318+603_318+606dup others(4): Show |
IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 5/5 | chr1 | 53923297 | ||||||
chr1:53923357
|
T | G | 4 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0138others(1): Show | 4 | HG02280.hp2 HG02615.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.318+547A>C | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 5/5 | chr1 | 53923357 | ||||||
chr1:53923413
|
G | A | 1 | a0001c0001t0001g0036 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.318+491C>T | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 5/5 | chr1 | 53923413 | ||||||
chr1:53923428
|
A | G | 1 | a0001c0001t0001g0082 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.318+476T>C | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 5/5 | chr1 | 53923428 | ||||||
chr1:53923440
|
C | T | 1 | a0001c0001t0001g0055 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.318+464G>A | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 5/5 | chr1 | 53923440 | ||||||
chr1:53923450
|
T | G | 3 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041 | 3 | HG01884.hp2 HG02559.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.318+454A>C | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 5/5 | chr1 | 53923450 | ||||||
chr1:53923527
|
A | G | 71 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(68): Show | 109 | HG00099.hp1 HG00280.hp1 HG00558.hp1 others(106): Show |
intron_variant | MODIFIER | c.318+377T>C | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 5/5 | chr1 | 53923527 | ||||||
chr1:53923632
|
A | G | 1 | a0001c0001t0001g0133 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.318+272T>C | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 5/5 | chr1 | 53923632 | ||||||
chr1:53923641
|
T | A | 1 | a0001c0001t0003g0033 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.318+263A>T | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 5/5 | chr1 | 53923641 | ||||||
chr1:53923741
|
A | G | 2 | a0001c0001t0001g0030a0001c0001t0001g0151 | 3 | HG02559.hp1 HG02976.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.318+163T>C | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 5/5 | chr1 | 53923741 | ||||||
chr1:53923798
|
C | A | 51 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(48): Show | 83 | HG00099.hp1 HG00280.hp1 HG00558.hp1 others(80): Show |
intron_variant | MODIFIER | c.318+106G>T | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 5/5 | chr1 | 53923798 | ||||||
chr1:53923844
|
G | GT | 59 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(56): Show | 96 | HG00099.hp1 HG00280.hp1 HG00558.hp1 others(93): Show |
intron_variant | MODIFIER | c.318+59dupA | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 5/5 | chr1 | 53923844 | ||||||
chr1:53923985
|
T | G | 8 | a0001c0001t0001g0025a0001c0001t0001g0105a0001c0001t0001g0106others(5): Show | 9 | HG01891.hp1 HG02615.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.275-38A>C | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 4/5 | chr1 | 53923985 | ||||||
chr1:53924101
|
TAG | T | 43 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(40): Show | 98 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(95): Show |
intron_variant | MODIFIER | c.275-156_275-155del others(2): Show |
IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 4/5 | chr1 | 53924101 | ||||||
chr1:53924258
|
TA | T | 6 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(3): Show | 6 | HG02280.hp2 HG02572.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.275-312delT | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 4/5 | chr1 | 53924258 | ||||||
chr1:53924346
|
A | T | 62 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(59): Show | 99 | HG00099.hp1 HG00280.hp1 HG00558.hp1 others(96): Show |
intron_variant | MODIFIER | c.275-399T>A | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 4/5 | chr1 | 53924346 | ||||||
chr1:53924359
|
T | C | 1 | a0001c0001t0001g0023 | 2 | NA19240.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.275-412A>G | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 4/5 | chr1 | 53924359 | ||||||
chr1:53924404
|
C | T | 2 | a0001c0001t0001g0137a0001c0001t0001g0139 | 2 | HG02615.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.275-457G>A | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 4/5 | chr1 | 53924404 | ||||||
chr1:53924511
|
C | T | 55 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(52): Show | 88 | HG00099.hp1 HG00280.hp1 HG00558.hp1 others(85): Show |
intron_variant | MODIFIER | c.275-564G>A | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 4/5 | chr1 | 53924511 | ||||||
chr1:53924521
|
G | T | 1 | a0001c0001t0001g0050 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.275-574C>A | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 4/5 | chr1 | 53924521 | ||||||
chr1:53924624
|
C | T | 1 | a0001c0001t0001g0038 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.275-677G>A | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 4/5 | chr1 | 53924624 | ||||||
chr1:53924629
|
G | A | 1 | a0001c0001t0001g0143 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.275-682C>T | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 4/5 | chr1 | 53924629 | ||||||
chr1:53924694
|
G | A | 1 | a0001c0001t0001g0128 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.275-747C>T | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 4/5 | chr1 | 53924694 | ||||||
chr1:53924754
|
G | A | 17 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0012others(14): Show | 38 | HG00280.hp1 HG00558.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.275-807C>T | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 4/5 | chr1 | 53924754 | ||||||
chr1:53924793
|
C | T | 19 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0017others(16): Show | 47 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(44): Show |
intron_variant | MODIFIER | c.275-846G>A | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 4/5 | chr1 | 53924793 | ||||||
chr1:53924861
|
T | C | 1 | a0001c0001t0001g0136 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.275-914A>G | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 4/5 | chr1 | 53924861 | ||||||
chr1:53924927
|
T | C | 1 | a0001c0001t0001g0083 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.275-980A>G | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 4/5 | chr1 | 53924927 | ||||||
chr1:53925001
|
C | T | 9 | a0001c0001t0001g0005a0001c0001t0001g0037a0001c0001t0001g0113others(6): Show | 15 | HG02109.hp1 HG02145.hp1 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.275-1054G>A | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 4/5 | chr1 | 53925001 | ||||||
chr1:53925263
|
C | G | 1 | a0001c0001t0001g0025 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.275-1316G>C | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 4/5 | chr1 | 53925263 | ||||||
chr1:53925319
|
A | G | 1 | a0001c0001t0001g0040 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.275-1372T>C | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 4/5 | chr1 | 53925319 | ||||||
chr1:53925327
|
T | A | 1 | a0001c0001t0001g0144 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.275-1380A>T | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 4/5 | chr1 | 53925327 | ||||||
chr1:53925467
|
T | C | 1 | a0001c0001t0001g0076 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.275-1520A>G | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 4/5 | chr1 | 53925467 | ||||||
chr1:53925558
|
G | A | 1 | a0001c0001t0001g0055 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.275-1611C>T | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 4/5 | chr1 | 53925558 | ||||||
chr1:53925582
|
G | A | 1 | a0001c0001t0001g0087 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.275-1635C>T | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 4/5 | chr1 | 53925582 | ||||||
chr1:53925650
|
G | C | 1 | a0001c0001t0001g0110 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.275-1703C>G | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 4/5 | chr1 | 53925650 | ||||||
chr1:53925888
|
G | A | 6 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(3): Show | 6 | HG02280.hp2 HG02572.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.275-1941C>T | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 4/5 | chr1 | 53925888 | ||||||
chr1:53926001
|
C | T | 4 | a0001c0001t0001g0027a0001c0001t0001g0029a0001c0001t0001g0125others(1): Show | 6 | HG00639.hp2 HG02886.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.275-2054G>A | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 4/5 | chr1 | 53926001 | ||||||
chr1:53926034
|
G | A | 1 | a0001c0001t0001g0045 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.275-2087C>T | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 4/5 | chr1 | 53926034 | ||||||
chr1:53926077
|
C | CA | 8 | a0001c0001t0001g0100a0001c0001t0001g0115a0001c0001t0001g0119others(5): Show | 8 | HG02145.hp1 HG02280.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.275-2131dupT | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 4/5 | chr1 | 53926077 | ||||||
chr1:53926077
|
CA | C | 7 | a0001c0001t0001g0026a0001c0001t0001g0049a0001c0001t0001g0080others(4): Show | 8 | HG01070.hp2 HG01243.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.275-2131delT | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 4/5 | chr1 | 53926077 | ||||||
chr1:53926171
|
G | A | 2 | a0001c0001t0001g0036a0001c0001t0001g0077 | 2 | HG02630.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.274+2201C>T | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 4/5 | chr1 | 53926171 | ||||||
chr1:53926198
|
T | G | 2 | a0001c0001t0001g0053a0001c0001t0001g0054 | 2 | HG03704.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.274+2174A>C | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 4/5 | chr1 | 53926198 | ||||||
chr1:53926393
|
C | T | 4 | a0001c0001t0001g0011a0001c0001t0001g0026a0001c0001t0001g0111others(1): Show | 8 | HG01243.hp1 HG02280.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.274+1979G>A | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 4/5 | chr1 | 53926393 | ||||||
chr1:53926529
|
TTAATA | T | 5 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(2): Show | 5 | HG02280.hp2 HG02615.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.274+1838_274+1842d others(7): Show |
IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 4/5 | chr1 | 53926529 | ||||||
chr1:53926565
|
C | T | 1 | a0001c0001t0001g0034 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.274+1807G>A | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 4/5 | chr1 | 53926565 | ||||||
chr1:53926629
|
C | G | 59 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(56): Show | 96 | HG00099.hp1 HG00280.hp1 HG00558.hp1 others(93): Show |
intron_variant | MODIFIER | c.274+1743G>C | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 4/5 | chr1 | 53926629 | ||||||
chr1:53926722
|
A | ATT | 11 | a0001c0001t0001g0120a0001c0001t0001g0132a0001c0001t0001g0135others(8): Show | 12 | HG01109.hp1 HG02055.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.274+1648_274+1649d others(4): Show |
IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 4/5 | chr1 | 53926722 | ||||||
chr1:53926857
|
C | T | 6 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(3): Show | 6 | HG02280.hp2 HG02572.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.274+1515G>A | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 4/5 | chr1 | 53926857 | ||||||
chr1:53926881
|
C | T | 1 | a0001c0001t0001g0038 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.274+1491G>A | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 4/5 | chr1 | 53926881 | ||||||
chr1:53927061
|
G | C | 2 | a0001c0001t0001g0113a0001c0001t0001g0119 | 2 | HG02145.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.274+1311C>G | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 4/5 | chr1 | 53927061 | ||||||
chr1:53927091
|
C | T | 6 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(3): Show | 6 | HG02280.hp2 HG02572.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.274+1281G>A | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 4/5 | chr1 | 53927091 | ||||||
chr1:53927186
|
TG | T | 2 | a0001c0001t0001g0024a0001c0001t0001g0087 | 3 | HG01496.hp1 HG01934.hp2 NA18941.hp1 |
intron_variant | MODIFIER | c.274+1185delC | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 4/5 | chr1 | 53927186 | ||||||
chr1:53927235
|
C | T | 1 | a0001c0001t0001g0145 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.274+1137G>A | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 4/5 | chr1 | 53927235 | ||||||
chr1:53927331
|
A | G | 28 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0027others(25): Show | 39 | HG00099.hp1 HG00639.hp2 HG01070.hp1 others(36): Show |
intron_variant | MODIFIER | c.274+1041T>C | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 4/5 | chr1 | 53927331 | ||||||
chr1:53927349
|
C | T | 1 | a0001c0001t0001g0105 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.274+1023G>A | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 4/5 | chr1 | 53927349 | ||||||
chr1:53927450
|
G | C | 10 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(7): Show | 11 | HG01109.hp1 HG02280.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.274+922C>G | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 4/5 | chr1 | 53927450 | ||||||
chr1:53927538
|
T | C | 4 | a0001c0001t0001g0011a0001c0001t0001g0026a0001c0001t0001g0111others(1): Show | 8 | HG01243.hp1 HG02280.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.274+834A>G | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 4/5 | chr1 | 53927538 | ||||||
chr1:53927770
|
T | G | 1 | a0001c0001t0001g0105 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.274+602A>C | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 4/5 | chr1 | 53927770 | ||||||
chr1:53927819
|
C | A | 17 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0012others(14): Show | 38 | HG00280.hp1 HG00558.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.274+553G>T | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 4/5 | chr1 | 53927819 | ||||||
chr1:53927838
|
A | G | 4 | a0001c0001t0002g0032a0001c0001t0002g0153a0001c0001t0002g0154others(1): Show | 5 | HG01109.hp1 HG02922.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.274+534T>C | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 4/5 | chr1 | 53927838 | ||||||
chr1:53927965
|
T | A | 4 | a0001c0001t0001g0027a0001c0001t0001g0029a0001c0001t0001g0125others(1): Show | 6 | HG00639.hp2 HG02886.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.274+407A>T | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 4/5 | chr1 | 53927965 | ||||||
chr1:53927988
|
T | C | 6 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(3): Show | 6 | HG02280.hp2 HG02572.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.274+384A>G | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 4/5 | chr1 | 53927988 | ||||||
chr1:53928134
|
C | T | 6 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(3): Show | 6 | HG02280.hp2 HG02572.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.274+238G>A | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 4/5 | chr1 | 53928134 | ||||||
chr1:53928220
|
T | C | 1 | a0001c0001t0001g0130 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.274+152A>G | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 4/5 | chr1 | 53928220 | ||||||
chr1:53928239
|
C | G | 1 | a0001c0001t0001g0108 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.274+133G>C | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 4/5 | chr1 | 53928239 | ||||||
chr1:53928342
|
T | C | 4 | a0001c0001t0001g0012a0001c0001t0001g0148a0001c0001t0001g0149others(1): Show | 7 | HG02080.hp2 NA18969.hp2 NA18973.hp1 others(4): Show |
intron_variant | MODIFIER | c.274+30A>G | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 4/5 | chr1 | 53928342 | ||||||
chr1:53928464
|
A | C | 2 | a0001c0001t0001g0120a0001c0001t0001g0132 | 2 | HG02055.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.206-24T>G | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 3/5 | chr1 | 53928464 | ||||||
chr1:53928468
|
T | C | 5 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0138others(2): Show | 5 | HG02280.hp2 HG02572.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.206-28A>G | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 3/5 | chr1 | 53928468 | ||||||
chr1:53928480
|
T | C | 4 | a0001c0001t0001g0027a0001c0001t0001g0029a0001c0001t0001g0125others(1): Show | 6 | HG00639.hp2 HG02886.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.206-40A>G | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 3/5 | chr1 | 53928480 | ||||||
chr1:53928605
|
T | C | 2 | a0001c0001t0001g0131a0001c0001t0001g0133 | 2 | NA19030.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.206-165A>G | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 3/5 | chr1 | 53928605 | ||||||
chr1:53928698
|
G | A | 1 | a0001c0001t0001g0069 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.206-258C>T | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 3/5 | chr1 | 53928698 | ||||||
chr1:53928714
|
T | C | 4 | a0001c0001t0001g0006a0001c0001t0001g0142a0001c0001t0001g0145others(1): Show | 10 | HG02145.hp2 HG02818.hp1 HG02896.hp2 others(7): Show |
intron_variant | MODIFIER | c.206-274A>G | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 3/5 | chr1 | 53928714 | ||||||
chr1:53928757
|
T | C | 3 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041 | 3 | HG01884.hp2 HG02559.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.206-317A>G | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 3/5 | chr1 | 53928757 | ||||||
chr1:53928768
|
T | C | 5 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(2): Show | 5 | HG02280.hp2 HG02615.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.206-328A>G | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 3/5 | chr1 | 53928768 | ||||||
chr1:53928994
|
T | C | 6 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(3): Show | 6 | HG02280.hp2 HG02572.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.206-554A>G | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 3/5 | chr1 | 53928994 | ||||||
chr1:53929062
|
T | C | 4 | a0001c0001t0001g0009a0001c0001t0001g0021a0001c0001t0001g0044others(1): Show | 8 | HG00408.hp2 HG02074.hp1 HG02155.hp2 others(5): Show |
intron_variant | MODIFIER | c.206-622A>G | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 3/5 | chr1 | 53929062 | ||||||
chr1:53929176
|
G | A | 17 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0012others(14): Show | 38 | HG00280.hp1 HG00558.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.206-736C>T | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 3/5 | chr1 | 53929176 | ||||||
chr1:53929304
|
C | T | 1 | a0001c0001t0001g0043 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.205+735G>A | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 3/5 | chr1 | 53929304 | ||||||
chr1:53929347
|
G | A | 1 | a0001c0001t0001g0063 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.205+692C>T | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 3/5 | chr1 | 53929347 | ||||||
chr1:53929696
|
A | ACT | 10 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(7): Show | 11 | HG01109.hp1 HG02280.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.205+342_205+343ins others(2): Show |
IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 3/5 | chr1 | 53929696 | ||||||
chr1:53929704
|
C | T | 3 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041 | 3 | HG01884.hp2 HG02559.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.205+335G>A | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 3/5 | chr1 | 53929704 | ||||||
chr1:53929764
|
A | T | 1 | a0001c0001t0001g0079 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.205+275T>A | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 3/5 | chr1 | 53929764 | ||||||
chr1:53929815
|
G | C | 59 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(56): Show | 96 | HG00099.hp1 HG00280.hp1 HG00558.hp1 others(93): Show |
intron_variant | MODIFIER | c.205+224C>G | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 3/5 | chr1 | 53929815 | ||||||
chr1:53929889
|
C | T | 6 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(3): Show | 6 | HG02280.hp2 HG02572.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.205+150G>A | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 3/5 | chr1 | 53929889 | ||||||
chr1:53930000
|
CA | C | 48 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(45): Show | 82 | HG00280.hp1 HG00558.hp1 HG00639.hp2 others(79): Show |
intron_variant | MODIFIER | c.205+38delT | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 3/5 | chr1 | 53930000 | ||||||
chr1:53930215
|
T | C | 1 | a0001c0001t0001g0084 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.99-70A>G | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53930215 | ||||||
chr1:53930410
|
C | T | 6 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(3): Show | 6 | HG02280.hp2 HG02572.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.99-265G>A | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53930410 | ||||||
chr1:53930554
|
G | GT | 7 | a0001c0001t0001g0119a0001c0001t0001g0135a0001c0001t0001g0136others(4): Show | 7 | HG02145.hp1 HG02280.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.99-410dupA | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53930554 | ||||||
chr1:53930577
|
G | C | 10 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(7): Show | 11 | HG01109.hp1 HG02280.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.99-432C>G | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53930577 | ||||||
chr1:53930653
|
C | T | 9 | a0001c0001t0001g0005a0001c0001t0001g0037a0001c0001t0001g0113others(6): Show | 15 | HG02109.hp1 HG02145.hp1 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.99-508G>A | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53930653 | ||||||
chr1:53931052
|
C | T | 59 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(56): Show | 96 | HG00099.hp1 HG00280.hp1 HG00558.hp1 others(93): Show |
intron_variant | MODIFIER | c.99-907G>A | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53931052 | ||||||
chr1:53931160
|
A | C | 2 | a0001c0001t0001g0106a0001c0001t0001g0109 | 2 | NA18956.hp2 NA18984.hp2 |
intron_variant | MODIFIER | c.99-1015T>G | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53931160 | ||||||
chr1:53931160
|
A | G | 4 | a0001c0001t0001g0011a0001c0001t0001g0026a0001c0001t0001g0111others(1): Show | 8 | HG01243.hp1 HG02280.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.99-1015T>C | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53931160 | ||||||
chr1:53931567
|
G | A | 17 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0012others(14): Show | 38 | HG00280.hp1 HG00558.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.99-1422C>T | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53931567 | ||||||
chr1:53931729
|
C | A | 1 | a0001c0001t0001g0026 | 2 | HG01243.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.99-1584G>T | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53931729 | ||||||
chr1:53931735
|
C | CT | 28 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0027others(25): Show | 39 | HG00099.hp1 HG00639.hp2 HG01070.hp1 others(36): Show |
intron_variant | MODIFIER | c.99-1591dupA | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53931735 | ||||||
chr1:53931737
|
T | C | 10 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(7): Show | 11 | HG01109.hp1 HG02280.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.99-1592A>G | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53931737 | ||||||
chr1:53931807
|
T | G | 1 | a0001c0001t0001g0045 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.99-1662A>C | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53931807 | ||||||
chr1:53931866
|
A | G | 1 | a0001c0001t0001g0073 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.99-1721T>C | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53931866 | ||||||
chr1:53931985
|
T | G | 4 | a0001c0001t0002g0032a0001c0001t0002g0153a0001c0001t0002g0154others(1): Show | 5 | HG01109.hp1 HG02922.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.99-1840A>C | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53931985 | ||||||
chr1:53932043
|
C | T | 1 | a0001c0001t0001g0037 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.99-1898G>A | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53932043 | ||||||
chr1:53932077
|
C | T | 3 | a0001c0001t0001g0137a0001c0001t0001g0138a0001c0001t0001g0139 | 3 | HG02280.hp2 HG02615.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.99-1932G>A | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53932077 | ||||||
chr1:53932104
|
C | A | 10 | a0001c0001t0001g0006a0001c0001t0001g0020a0001c0001t0001g0030others(7): Show | 19 | HG01167.hp1 HG01884.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.99-1959G>T | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53932104 | ||||||
chr1:53932179
|
C | T | 4 | a0001c0001t0002g0032a0001c0001t0002g0153a0001c0001t0002g0154others(1): Show | 5 | HG01109.hp1 HG02922.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.99-2034G>A | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53932179 | ||||||
chr1:53932183
|
T | C | 2 | a0001c0001t0001g0042a0001c0001t0001g0085 | 2 | HG01243.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.99-2038A>G | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53932183 | ||||||
chr1:53932214
|
G | A | 1 | a0001c0001t0001g0102 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.99-2069C>T | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53932214 | ||||||
chr1:53932333
|
C | CA | 43 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(40): Show | 76 | HG00099.hp1 HG00280.hp1 HG00558.hp1 others(73): Show |
intron_variant | MODIFIER | c.99-2189dupT | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53932333 | ||||||
chr1:53932405
|
T | G | 2 | a0001c0001t0001g0120a0001c0001t0001g0132 | 2 | HG02055.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.99-2260A>C | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53932405 | ||||||
chr1:53932407
|
C | T | 1 | a0001c0001t0001g0131 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.99-2262G>A | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53932407 | ||||||
chr1:53932473
|
T | C | 1 | a0001c0001t0001g0103 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.99-2328A>G | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53932473 | ||||||
chr1:53932494
|
T | C | 1 | a0001c0001t0001g0086 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.99-2349A>G | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53932494 | ||||||
chr1:53932522
|
T | C | 4 | a0001c0001t0001g0011a0001c0001t0001g0026a0001c0001t0001g0111others(1): Show | 8 | HG01243.hp1 HG02280.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.99-2377A>G | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53932522 | ||||||
chr1:53932545
|
A | G | 4 | a0001c0001t0001g0007a0001c0001t0001g0049a0001c0001t0001g0050others(1): Show | 8 | HG00423.hp2 HG00438.hp1 HG02083.hp2 others(5): Show |
intron_variant | MODIFIER | c.99-2400T>C | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53932545 | ||||||
chr1:53932648
|
T | C | 4 | a0001c0001t0001g0027a0001c0001t0001g0029a0001c0001t0001g0125others(1): Show | 6 | HG00639.hp2 HG02886.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.99-2503A>G | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53932648 | ||||||
chr1:53932755
|
G | T | 4 | a0001c0001t0001g0011a0001c0001t0001g0026a0001c0001t0001g0111others(1): Show | 8 | HG01243.hp1 HG02280.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.99-2610C>A | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53932755 | ||||||
chr1:53932787
|
C | A | 10 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(7): Show | 11 | HG01109.hp1 HG02280.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.99-2642G>T | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53932787 | ||||||
chr1:53933106
|
A | G | 1 | a0001c0001t0001g0037 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.99-2961T>C | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53933106 | ||||||
chr1:53933135
|
C | CT | 14 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0026others(11): Show | 23 | HG00099.hp1 HG01070.hp1 HG01243.hp1 others(20): Show |
intron_variant | MODIFIER | c.99-2991dupA | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53933135 | ||||||
chr1:53933135
|
C | CTT | 7 | a0001c0001t0001g0120a0001c0001t0001g0121a0001c0001t0001g0132others(4): Show | 7 | HG02055.hp1 HG02109.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.99-2992_99-2991dup others(2): Show |
IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53933135 | ||||||
chr1:53933135
|
CT | C | 12 | a0001c0001t0001g0006a0001c0001t0001g0020a0001c0001t0001g0030others(9): Show | 21 | HG01167.hp1 HG01884.hp1 HG02145.hp2 others(18): Show |
intron_variant | MODIFIER | c.99-2991delA | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53933135 | ||||||
chr1:53933159
|
G | A | 1 | a0001c0001t0001g0095 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.99-3014C>T | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53933159 | ||||||
chr1:53933188
|
C | T | 2 | a0001c0001t0001g0062a0001c0001t0001g0075 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.99-3043G>A | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53933188 | ||||||
chr1:53933220
|
C | T | 6 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(3): Show | 6 | HG02280.hp2 HG02572.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.99-3075G>A | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53933220 | ||||||
chr1:53933265
|
A | G | 10 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(7): Show | 11 | HG01109.hp1 HG02280.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.99-3120T>C | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53933265 | ||||||
chr1:53933283
|
C | T | 1 | a0001c0001t0001g0053 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.99-3138G>A | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53933283 | ||||||
chr1:53933303
|
T | C | 1 | a0001c0001t0001g0088 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.99-3158A>G | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53933303 | ||||||
chr1:53933355
|
C | T | 4 | a0001c0001t0001g0027a0001c0001t0001g0029a0001c0001t0001g0125others(1): Show | 6 | HG00639.hp2 HG02886.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.99-3210G>A | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53933355 | ||||||
chr1:53933408
|
G | A | 10 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(7): Show | 11 | HG01109.hp1 HG02280.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.99-3263C>T | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53933408 | ||||||
chr1:53933413
|
C | T | 4 | a0001c0001t0001g0016a0001c0001t0001g0062a0001c0001t0001g0075others(1): Show | 6 | HG00738.hp2 HG01106.hp1 HG01257.hp2 others(3): Show |
intron_variant | MODIFIER | c.99-3268G>A | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53933413 | ||||||
chr1:53933429
|
C | T | 45 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(42): Show | 77 | HG00099.hp1 HG00280.hp1 HG00558.hp1 others(74): Show |
intron_variant | MODIFIER | c.99-3284G>A | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53933429 | ||||||
chr1:53933562
|
T | C | 1 | a0001c0001t0001g0040 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.99-3417A>G | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53933562 | ||||||
chr1:53933571
|
C | T | 1 | a0001c0001t0001g0074 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.99-3426G>A | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53933571 | ||||||
chr1:53933832
|
A | T | 3 | a0001c0001t0001g0015a0001c0001t0001g0073a0001c0001t0001g0092 | 5 | NA18952.hp1 NA18959.hp2 NA18982.hp1 others(2): Show |
intron_variant | MODIFIER | c.99-3687T>A | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53933832 | ||||||
chr1:53933853
|
AT | A | 6 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(3): Show | 6 | HG02280.hp2 HG02572.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.99-3709delA | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53933853 | ||||||
chr1:53933870
|
C | T | 2 | a0001c0001t0001g0114a0001c0001t0001g0115 | 2 | HG02976.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.99-3725G>A | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53933870 | ||||||
chr1:53933916
|
C | T | 3 | a0001c0001t0001g0008a0001c0001t0001g0103a0001c0001t0001g0104 | 7 | HG00544.hp1 HG03490.hp1 HG03492.hp2 others(4): Show |
intron_variant | MODIFIER | c.99-3771G>A | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53933916 | ||||||
chr1:53934066
|
C | G | 4 | a0001c0001t0002g0032a0001c0001t0002g0153a0001c0001t0002g0154others(1): Show | 5 | HG01109.hp1 HG02922.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.99-3921G>C | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53934066 | ||||||
chr1:53934152
|
C | T | 13 | a0001c0001t0001g0019a0001c0001t0001g0028a0001c0001t0001g0121others(10): Show | 16 | HG00099.hp1 HG01070.hp1 HG01255.hp1 others(13): Show |
intron_variant | MODIFIER | c.99-4007G>A | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53934152 | ||||||
chr1:53934586
|
C | T | 1 | a0001c0001t0001g0072 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.99-4441G>A | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53934586 | ||||||
chr1:53934615
|
T | C | 4 | a0001c0001t0002g0032a0001c0001t0002g0153a0001c0001t0002g0154others(1): Show | 5 | HG01109.hp1 HG02922.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.99-4470A>G | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53934615 | ||||||
chr1:53934626
|
T | C | 2 | a0001c0001t0001g0053a0001c0001t0001g0054 | 2 | HG03704.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.99-4481A>G | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53934626 | ||||||
chr1:53934668
|
T | C | 1 | a0001c0001t0001g0126 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.99-4523A>G | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53934668 | ||||||
chr1:53934671
|
G | C | 17 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0012others(14): Show | 38 | HG00280.hp1 HG00558.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.99-4526C>G | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53934671 | ||||||
chr1:53934915
|
C | T | 1 | a0001c0001t0001g0071 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.99-4770G>A | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53934915 | ||||||
chr1:53934954
|
G | A | 26 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0027others(23): Show | 37 | HG00099.hp1 HG00639.hp2 HG01070.hp1 others(34): Show |
intron_variant | MODIFIER | c.99-4809C>T | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53934954 | ||||||
chr1:53935001
|
A | G | 13 | a0001c0001t0001g0019a0001c0001t0001g0028a0001c0001t0001g0121others(10): Show | 16 | HG00099.hp1 HG01070.hp1 HG01255.hp1 others(13): Show |
intron_variant | MODIFIER | c.99-4856T>C | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53935001 | ||||||
chr1:53935027
|
C | T | 4 | a0001c0001t0002g0032a0001c0001t0002g0153a0001c0001t0002g0154others(1): Show | 5 | HG01109.hp1 HG02922.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.99-4882G>A | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53935027 | ||||||
chr1:53935104
|
A | G | 1 | a0001c0001t0001g0070 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.98+4881T>C | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53935104 | ||||||
chr1:53935106
|
G | A | 1 | a0001c0001t0001g0135 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.98+4879C>T | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53935106 | ||||||
chr1:53935124
|
G | T | 4 | a0001c0001t0002g0032a0001c0001t0002g0153a0001c0001t0002g0154others(1): Show | 5 | HG01109.hp1 HG02922.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.98+4861C>A | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53935124 | ||||||
chr1:53935206
|
G | C | 4 | a0001c0001t0002g0032a0001c0001t0002g0153a0001c0001t0002g0154others(1): Show | 5 | HG01109.hp1 HG02922.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.98+4779C>G | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53935206 | ||||||
chr1:53935283
|
G | A | 2 | a0001c0001t0001g0120a0001c0001t0001g0132 | 2 | HG02055.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.98+4702C>T | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53935283 | ||||||
chr1:53935450
|
T | TGTGTGGG others(2154): Show |
1 | a0001c0001t0002g0155 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.98+4534_98+4535ins others(2161): Show |
IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53935450 | ||||||
chr1:53935450
|
T | TGTGTGGG others(2153): Show |
1 | a0001c0001t0002g0153 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.98+4534_98+4535ins others(2160): Show |
IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53935450 | ||||||
chr1:53935450
|
T | TGTGTGGG others(2153): Show |
1 | a0001c0001t0002g0032 | 2 | HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.98+4534_98+4535ins others(2160): Show |
IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53935450 | ||||||
chr1:53935450
|
T | TGTGTGGG others(2154): Show |
1 | a0001c0001t0002g0154 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.98+4534_98+4535ins others(2161): Show |
IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53935450 | ||||||
chr1:53935481
|
C | T | 10 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(7): Show | 11 | HG01109.hp1 HG02280.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.98+4504G>A | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53935481 | ||||||
chr1:53935534
|
G | GCCACTGA others(309): Show |
4 | a0001c0001t0002g0032a0001c0001t0002g0153a0001c0001t0002g0154others(1): Show | 5 | HG01109.hp1 HG02922.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.98+4450_98+4451ins others(316): Show |
IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53935534 | ||||||
chr1:53935602
|
A | AC | 3 | a0001c0001t0001g0137a0001c0001t0001g0138a0001c0001t0002g0153 | 3 | HG01109.hp1 HG02280.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.98+4382dupG | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53935602 | ||||||
chr1:53935606
|
A | C | 10 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(7): Show | 11 | HG01109.hp1 HG02280.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.98+4379T>G | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53935606 | ||||||
chr1:53935630
|
C | CT | 9 | a0001c0001t0001g0011a0001c0001t0001g0026a0001c0001t0001g0111others(6): Show | 14 | HG01109.hp1 HG01243.hp1 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.98+4354dupA | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53935630 | ||||||
chr1:53935630
|
CT | C | 19 | a0001c0001t0001g0019a0001c0001t0001g0028a0001c0001t0001g0121others(16): Show | 22 | HG00099.hp1 HG01070.hp1 HG01255.hp1 others(19): Show |
intron_variant | MODIFIER | c.98+4354delA | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53935630 | ||||||
chr1:53935653
|
A | G | 1 | a0001c0001t0001g0090 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.98+4332T>C | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53935653 | ||||||
chr1:53935905
|
T | C | 4 | a0001c0001t0001g0027a0001c0001t0001g0029a0001c0001t0001g0125others(1): Show | 6 | HG00639.hp2 HG02886.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.98+4080A>G | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53935905 | ||||||
chr1:53936049
|
C | T | 4 | a0001c0001t0002g0032a0001c0001t0002g0153a0001c0001t0002g0154others(1): Show | 5 | HG01109.hp1 HG02922.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.98+3936G>A | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53936049 | ||||||
chr1:53936095
|
T | TA | 6 | a0001c0001t0001g0120a0001c0001t0001g0132a0001c0001t0002g0032others(3): Show | 7 | HG01109.hp1 HG02055.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.98+3889dupT | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53936095 | ||||||
chr1:53936157
|
G | A | 9 | a0001c0001t0001g0005a0001c0001t0001g0037a0001c0001t0001g0113others(6): Show | 15 | HG02109.hp1 HG02145.hp1 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.98+3828C>T | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53936157 | ||||||
chr1:53936224
|
G | A | 2 | a0001c0001t0001g0121a0001c0001t0001g0122 | 2 | HG01255.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.98+3761C>T | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53936224 | ||||||
chr1:53936295
|
C | G | 2 | a0001c0001t0001g0121a0001c0001t0001g0122 | 2 | HG01255.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.98+3690G>C | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53936295 | ||||||
chr1:53936441
|
C | A | 45 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(42): Show | 77 | HG00099.hp1 HG00280.hp1 HG00558.hp1 others(74): Show |
intron_variant | MODIFIER | c.98+3544G>T | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53936441 | ||||||
chr1:53936532
|
G | A | 1 | a0001c0001t0001g0130 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.98+3453C>T | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53936532 | ||||||
chr1:53936597
|
C | G | 6 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(3): Show | 6 | HG02280.hp2 HG02572.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.98+3388G>C | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53936597 | ||||||
chr1:53936642
|
A | C | 3 | a0001c0001t0001g0014a0001c0001t0001g0023a0001c0001t0001g0069 | 6 | HG01891.hp2 HG02809.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.98+3343T>G | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53936642 | ||||||
chr1:53936730
|
C | T | 5 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(2): Show | 5 | HG02280.hp2 HG02615.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.98+3255G>A | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53936730 | ||||||
chr1:53936884
|
G | A | 6 | a0001c0001t0001g0005a0001c0001t0001g0037a0001c0001t0001g0113others(3): Show | 12 | HG02109.hp1 HG02145.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.98+3101C>T | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53936884 | ||||||
chr1:53937171
|
G | A | 4 | a0001c0001t0002g0032a0001c0001t0002g0153a0001c0001t0002g0154others(1): Show | 5 | HG01109.hp1 HG02922.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.98+2814C>T | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53937171 | ||||||
chr1:53937244
|
G | C | 1 | a0001c0001t0001g0112 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.98+2741C>G | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53937244 | ||||||
chr1:53937341
|
ACTT | A | 3 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041 | 3 | HG01884.hp2 HG02559.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.98+2641_98+2643del others(3): Show |
IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53937341 | ||||||
chr1:53937493
|
G | A | 1 | a0001c0001t0001g0025 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.98+2492C>T | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53937493 | ||||||
chr1:53937778
|
T | G | 2 | a0001c0001t0001g0120a0001c0001t0001g0132 | 2 | HG02055.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.98+2207A>C | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53937778 | ||||||
chr1:53937784
|
G | A | 1 | a0001c0001t0001g0089 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.98+2201C>T | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53937784 | ||||||
chr1:53937791
|
A | G | 5 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0107others(2): Show | 5 | HG01891.hp1 HG02895.hp1 NA18956.hp2 others(2): Show |
intron_variant | MODIFIER | c.98+2194T>C | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53937791 | ||||||
chr1:53937889
|
T | C | 1 | a0001c0001t0001g0031 | 2 | HG00673.hp1 HG02132.hp1 |
intron_variant | MODIFIER | c.98+2096A>G | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53937889 | ||||||
chr1:53938008
|
C | T | 1 | a0001c0001t0001g0068 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.98+1977G>A | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53938008 | ||||||
chr1:53938022
|
C | G | 1 | a0001c0001t0003g0033 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.98+1963G>C | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53938022 | ||||||
chr1:53938313
|
T | C | 1 | a0001c0001t0003g0033 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.98+1672A>G | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53938313 | ||||||
chr1:53938360
|
A | G | 1 | a0001c0001t0001g0067 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.98+1625T>C | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53938360 | ||||||
chr1:53938375
|
A | G | 2 | a0001c0001t0001g0120a0001c0001t0001g0132 | 2 | HG02055.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.98+1610T>C | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53938375 | ||||||
chr1:53938633
|
T | A | 9 | a0001c0001t0001g0005a0001c0001t0001g0037a0001c0001t0001g0113others(6): Show | 15 | HG02109.hp1 HG02145.hp1 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.98+1352A>T | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53938633 | ||||||
chr1:53938638
|
C | T | 1 | a0001c0001t0001g0041 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.98+1347G>A | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53938638 | ||||||
chr1:53938683
|
G | C | 4 | a0001c0001t0001g0027a0001c0001t0001g0029a0001c0001t0001g0125others(1): Show | 6 | HG00639.hp2 HG02886.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.98+1302C>G | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53938683 | ||||||
chr1:53938813
|
G | A | 4 | a0001c0001t0001g0027a0001c0001t0001g0029a0001c0001t0001g0125others(1): Show | 6 | HG00639.hp2 HG02886.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.98+1172C>T | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53938813 | ||||||
chr1:53938849
|
C | T | 45 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(42): Show | 77 | HG00099.hp1 HG00280.hp1 HG00558.hp1 others(74): Show |
intron_variant | MODIFIER | c.98+1136G>A | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53938849 | ||||||
chr1:53938873
|
G | T | 6 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(3): Show | 6 | HG02280.hp2 HG02572.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.98+1112C>A | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53938873 | ||||||
chr1:53938976
|
A | G | 1 | a0001c0001t0001g0066 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.98+1009T>C | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53938976 | ||||||
chr1:53938992
|
T | C | 1 | a0001c0001t0001g0146 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.98+993A>G | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53938992 | ||||||
chr1:53939035
|
T | C | 1 | a0001c0001t0001g0136 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.98+950A>G | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53939035 | ||||||
chr1:53939074
|
C | CA | 34 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(31): Show | 68 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(65): Show |
intron_variant | MODIFIER | c.98+910dupT | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53939074 | ||||||
chr1:53939074
|
C | CAA | 11 | a0001c0001t0001g0011a0001c0001t0001g0047a0001c0001t0001g0091others(8): Show | 14 | HG02055.hp1 HG02074.hp1 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.98+909_98+910dupTT | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53939074 | ||||||
chr1:53939074
|
CA | C | 14 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0048others(11): Show | 14 | HG01070.hp2 HG01257.hp2 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.98+910delT | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53939074 | ||||||
chr1:53939074
|
CAAAAAAA others(4): Show |
C | 1 | a0001c0001t0001g0059 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.98+900_98+910delTT others(9): Show |
IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53939074 | ||||||
chr1:53939167
|
G | A | 1 | a0001c0001t0001g0150 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.98+818C>T | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53939167 | ||||||
chr1:53939219
|
A | G | 59 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(56): Show | 96 | HG00099.hp1 HG00280.hp1 HG00558.hp1 others(93): Show |
intron_variant | MODIFIER | c.98+766T>C | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53939219 | ||||||
chr1:53939288
|
G | A | 1 | a0001c0001t0001g0041 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.98+697C>T | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53939288 | ||||||
chr1:53939321
|
T | G | 10 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(7): Show | 11 | HG01109.hp1 HG02280.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.98+664A>C | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53939321 | ||||||
chr1:53939369
|
T | C | 10 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(7): Show | 11 | HG01109.hp1 HG02280.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.98+616A>G | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53939369 | ||||||
chr1:53939390
|
C | CA | 13 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0001g0094others(10): Show | 14 | HG01109.hp1 HG02145.hp1 HG02738.hp1 others(11): Show |
intron_variant | MODIFIER | c.98+594dupT | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53939390 | ||||||
chr1:53939390
|
CA | C | 8 | a0001c0001t0001g0011a0001c0001t0001g0026a0001c0001t0001g0057others(5): Show | 12 | HG01169.hp2 HG01243.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.98+594delT | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53939390 | ||||||
chr1:53939536
|
G | A | 1 | a0001c0001t0001g0059 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.98+449C>T | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53939536 | ||||||
chr1:53939540
|
A | G | 1 | a0001c0001t0001g0059 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.98+445T>C | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53939540 | ||||||
chr1:53939676
|
C | T | 6 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(3): Show | 6 | HG02280.hp2 HG02572.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.98+309G>A | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53939676 | ||||||
chr1:53939888
|
C | G | 1 | a0001c0001t0001g0058 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.98+97G>C | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53939888 | ||||||
chr1:53939953
|
G | T | 1 | a0001c0001t0001g0057 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.98+32C>A | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53939953 | ||||||
chr1:53939954
|
A | G | 4 | a0001c0001t0001g0027a0001c0001t0001g0029a0001c0001t0001g0125others(1): Show | 6 | HG00639.hp2 HG02886.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.98+31T>C | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53939954 | ||||||
chr1:53939976
|
A | G | 1 | a0001c0001t0001g0148 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.98+9T>C | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53939976 | ||||||
chr1:53939979
|
T | G | 3 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041 | 3 | HG01884.hp2 HG02559.hp2 HG02723.hp2 |
splice_region_variant&intron_variant | LOW | c.98+6A>C | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53939979 | ||||||
chr1:53940167
|
A | G | 1 | a0001c0001t0001g0124 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-15-70T>C | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 1/5 | chr1 | 53940167 | ||||||
chr1:53940346
|
A | G | 1 | a0001c0001t0001g0056 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.-15-249T>C | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 1/5 | chr1 | 53940346 | ||||||
chr1:53940383
|
G | A | 1 | a0001c0001t0001g0029 | 2 | HG02886.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-15-286C>T | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 1/5 | chr1 | 53940383 | ||||||
chr1:53940413
|
C | T | 1 | a0001c0001t0001g0136 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-15-316G>A | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 1/5 | chr1 | 53940413 | ||||||
chr1:53940421
|
T | C | 10 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(7): Show | 11 | HG01109.hp1 HG02280.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.-15-324A>G | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 1/5 | chr1 | 53940421 | ||||||
chr1:53940447
|
A | G | 1 | a0001c0001t0001g0142 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-15-350T>C | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 1/5 | chr1 | 53940447 | ||||||
chr1:53940476
|
A | G | 5 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(2): Show | 5 | HG02280.hp2 HG02615.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.-15-379T>C | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 1/5 | chr1 | 53940476 | ||||||
chr1:53940694
|
A | G | 4 | a0001c0001t0002g0032a0001c0001t0002g0153a0001c0001t0002g0154others(1): Show | 5 | HG01109.hp1 HG02922.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.-15-597T>C | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 1/5 | chr1 | 53940694 | ||||||
chr1:53940840
|
G | C | 4 | a0001c0001t0001g0011a0001c0001t0001g0026a0001c0001t0001g0111others(1): Show | 8 | HG01243.hp1 HG02280.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.-15-743C>G | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 1/5 | chr1 | 53940840 | ||||||
chr1:53940891
|
C | G | 1 | a0001c0001t0001g0055 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-15-794G>C | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 1/5 | chr1 | 53940891 | ||||||
chr1:53940895
|
A | C | 1 | a0001c0001t0001g0048 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-15-798T>G | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 1/5 | chr1 | 53940895 | ||||||
chr1:53940954
|
A | T | 4 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0054others(1): Show | 4 | HG02615.hp2 HG02717.hp2 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.-15-857T>A | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 1/5 | chr1 | 53940954 | ||||||
chr1:53940954
|
AT | A | 6 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(3): Show | 6 | HG02280.hp2 HG02572.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.-15-858delA | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 1/5 | chr1 | 53940954 | ||||||
chr1:53940954
|
ATT | A | 7 | a0001c0001t0001g0004a0001c0001t0001g0012a0001c0001t0001g0031others(4): Show | 19 | HG00280.hp1 HG00558.hp1 HG00673.hp1 others(16): Show |
intron_variant | MODIFIER | c.-15-859_-15-858del others(2): Show |
IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 1/5 | chr1 | 53940954 | ||||||
chr1:53941064
|
G | T | 1 | a0001c0001t0001g0048 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-15-967C>A | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 1/5 | chr1 | 53941064 | ||||||
chr1:53941087
|
C | T | 3 | a0001c0001t0001g0022a0001c0001t0001g0101a0001c0001t0001g0102 | 4 | HG01257.hp1 HG01515.hp1 HG02055.hp2 others(1): Show |
intron_variant | MODIFIER | c.-15-990G>A | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 1/5 | chr1 | 53941087 | ||||||
chr1:53941151
|
C | T | 4 | a0001c0001t0001g0007a0001c0001t0001g0049a0001c0001t0001g0050others(1): Show | 8 | HG00423.hp2 HG00438.hp1 HG02083.hp2 others(5): Show |
intron_variant | MODIFIER | c.-15-1054G>A | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 1/5 | chr1 | 53941151 | ||||||
chr1:53941169
|
A | G | 1 | a0001c0001t0001g0042 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-15-1072T>C | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 1/5 | chr1 | 53941169 | ||||||
chr1:53941204
|
T | A | 1 | a0001c0001t0001g0048 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-15-1107A>T | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 1/5 | chr1 | 53941204 | ||||||
chr1:53941278
|
C | T | 10 | a0001c0001t0001g0009a0001c0001t0001g0013a0001c0001t0001g0021others(7): Show | 16 | HG00408.hp2 HG02040.hp2 HG02074.hp1 others(13): Show |
intron_variant | MODIFIER | c.-15-1181G>A | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 1/5 | chr1 | 53941278 | ||||||
chr1:53941283
|
G | A | 6 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(3): Show | 6 | HG02280.hp2 HG02572.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.-15-1186C>T | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 1/5 | chr1 | 53941283 | ||||||
chr1:53941327
|
T | C | 1 | a0001c0001t0001g0151 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-15-1230A>G | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 1/5 | chr1 | 53941327 | ||||||
chr1:53941386
|
G | A | 4 | a0001c0001t0001g0011a0001c0001t0001g0026a0001c0001t0001g0111others(1): Show | 8 | HG01243.hp1 HG02280.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.-15-1289C>T | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 1/5 | chr1 | 53941386 | ||||||
chr1:53941405
|
T | G | 2 | a0001c0001t0001g0024a0001c0001t0001g0099 | 3 | HG01496.hp1 HG01934.hp2 HG02273.hp1 |
intron_variant | MODIFIER | c.-15-1308A>C | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 1/5 | chr1 | 53941405 | ||||||
chr1:53941430
|
T | C | 4 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0138others(1): Show | 4 | HG02280.hp2 HG02615.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.-15-1333A>G | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 1/5 | chr1 | 53941430 | ||||||
chr1:53941848
|
C | T | 71 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(68): Show | 109 | HG00099.hp1 HG00280.hp1 HG00558.hp1 others(106): Show |
intron_variant | MODIFIER | c.-15-1751G>A | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 1/5 | chr1 | 53941848 | ||||||
chr1:53941890
|
C | T | 3 | a0001c0001t0001g0011a0001c0001t0001g0111a0001c0001t0001g0112 | 6 | HG02572.hp2 HG02647.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.-15-1793G>A | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 1/5 | chr1 | 53941890 | ||||||
chr1:53941938
|
T | C | 1 | a0001c0001t0001g0110 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-15-1841A>G | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 1/5 | chr1 | 53941938 | ||||||
chr1:53942106
|
G | C | 5 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(2): Show | 5 | HG02280.hp2 HG02615.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.-15-2009C>G | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 1/5 | chr1 | 53942106 | ||||||
chr1:53942191
|
T | G | 1 | a0001c0001t0001g0100 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.-15-2094A>C | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 1/5 | chr1 | 53942191 | ||||||
chr1:53942225
|
A | G | 4 | a0001c0001t0002g0032a0001c0001t0002g0153a0001c0001t0002g0154others(1): Show | 5 | HG01109.hp1 HG02922.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.-15-2128T>C | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 1/5 | chr1 | 53942225 | ||||||
chr1:53942436
|
G | T | 4 | a0001c0001t0002g0032a0001c0001t0002g0153a0001c0001t0002g0154others(1): Show | 5 | HG01109.hp1 HG02922.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.-15-2339C>A | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 1/5 | chr1 | 53942436 | ||||||
chr1:53942469
|
C | T | 4 | a0001c0001t0002g0032a0001c0001t0002g0153a0001c0001t0002g0154others(1): Show | 5 | HG01109.hp1 HG02922.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.-15-2372G>A | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 1/5 | chr1 | 53942469 | ||||||
chr1:53942606
|
T | C | 2 | a0001c0001t0001g0101a0001c0001t0001g0102 | 2 | HG01257.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.-15-2509A>G | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 1/5 | chr1 | 53942606 | ||||||
chr1:53942633
|
T | C | 10 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(7): Show | 11 | HG01109.hp1 HG02280.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.-15-2536A>G | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 1/5 | chr1 | 53942633 | ||||||
chr1:53942752
|
T | C | 4 | a0001c0001t0002g0032a0001c0001t0002g0153a0001c0001t0002g0154others(1): Show | 5 | HG01109.hp1 HG02922.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.-15-2655A>G | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 1/5 | chr1 | 53942752 | ||||||
chr1:53942769
|
A | C | 10 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(7): Show | 11 | HG01109.hp1 HG02280.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.-15-2672T>G | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 1/5 | chr1 | 53942769 | ||||||
chr1:53942878
|
C | T | 4 | a0001c0001t0001g0019a0001c0001t0001g0121a0001c0001t0001g0122others(1): Show | 6 | HG00099.hp1 HG01070.hp1 HG01255.hp1 others(3): Show |
intron_variant | MODIFIER | c.-16+2677G>A | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 1/5 | chr1 | 53942878 | ||||||
chr1:53942892
|
A | C | 1 | a0001c0001t0001g0042 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-16+2663T>G | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 1/5 | chr1 | 53942892 | ||||||
chr1:53942912
|
C | G | 71 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(68): Show | 109 | HG00099.hp1 HG00280.hp1 HG00558.hp1 others(106): Show |
intron_variant | MODIFIER | c.-16+2643G>C | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 1/5 | chr1 | 53942912 | ||||||
chr1:53942962
|
A | T | 4 | a0001c0001t0001g0011a0001c0001t0001g0026a0001c0001t0001g0111others(1): Show | 8 | HG01243.hp1 HG02280.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.-16+2593T>A | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 1/5 | chr1 | 53942962 | ||||||
chr1:53943021
|
C | T | 1 | a0001c0001t0001g0120 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-16+2534G>A | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 1/5 | chr1 | 53943021 | ||||||
chr1:53943076
|
C | CT | 9 | a0001c0001t0001g0005a0001c0001t0001g0037a0001c0001t0001g0113others(6): Show | 15 | HG02109.hp1 HG02145.hp1 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.-16+2478dupA | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 1/5 | chr1 | 53943076 | ||||||
chr1:53943164
|
T | G | 6 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(3): Show | 6 | HG02280.hp2 HG02572.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.-16+2391A>C | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 1/5 | chr1 | 53943164 | ||||||
chr1:53943207
|
A | C | 4 | a0001c0001t0001g0011a0001c0001t0001g0026a0001c0001t0001g0111others(1): Show | 8 | HG01243.hp1 HG02280.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.-16+2348T>G | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 1/5 | chr1 | 53943207 | ||||||
chr1:53943245
|
G | C | 10 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(7): Show | 11 | HG01109.hp1 HG02280.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.-16+2310C>G | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 1/5 | chr1 | 53943245 | ||||||
chr1:53943275
|
A | G | 1 | a0001c0001t0003g0033 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-16+2280T>C | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 1/5 | chr1 | 53943275 | ||||||
chr1:53943415
|
G | GGT | 4 | a0001c0001t0002g0032a0001c0001t0002g0153a0001c0001t0002g0154others(1): Show | 5 | HG01109.hp1 HG02922.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.-16+2138_-16+2139d others(4): Show |
IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 1/5 | chr1 | 53943415 | ||||||
chr1:53943482
|
G | GGA | 59 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(56): Show | 96 | HG00099.hp1 HG00280.hp1 HG00558.hp1 others(93): Show |
intron_variant | MODIFIER | c.-16+2071_-16+2072d others(4): Show |
IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 1/5 | chr1 | 53943482 | ||||||
chr1:53943511
|
G | A | 10 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(7): Show | 11 | HG01109.hp1 HG02280.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.-16+2044C>T | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 1/5 | chr1 | 53943511 | ||||||
chr1:53943593
|
G | A | 1 | a0001c0001t0001g0135 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-16+1962C>T | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 1/5 | chr1 | 53943593 | ||||||
chr1:53943620
|
G | A | 4 | a0001c0001t0002g0032a0001c0001t0002g0153a0001c0001t0002g0154others(1): Show | 5 | HG01109.hp1 HG02922.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.-16+1935C>T | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 1/5 | chr1 | 53943620 | ||||||
chr1:53943882
|
A | G | 1 | a0001c0001t0001g0141 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.-16+1673T>C | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 1/5 | chr1 | 53943882 | ||||||
chr1:53943885
|
G | C | 3 | a0001c0001t0001g0008a0001c0001t0001g0103a0001c0001t0001g0104 | 7 | HG00544.hp1 HG03490.hp1 HG03492.hp2 others(4): Show |
intron_variant | MODIFIER | c.-16+1670C>G | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 1/5 | chr1 | 53943885 | ||||||
chr1:53943981
|
G | T | 6 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(3): Show | 6 | HG02280.hp2 HG02572.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.-16+1574C>A | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 1/5 | chr1 | 53943981 | ||||||
chr1:53944138
|
T | C | 4 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0138others(1): Show | 4 | HG02280.hp2 HG02615.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.-16+1417A>G | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 1/5 | chr1 | 53944138 | ||||||
chr1:53944279
|
G | A | 8 | a0001c0001t0001g0025a0001c0001t0001g0105a0001c0001t0001g0106others(5): Show | 9 | HG01891.hp1 HG02615.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.-16+1276C>T | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 1/5 | chr1 | 53944279 | ||||||
chr1:53944344
|
T | A | 17 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0012others(14): Show | 38 | HG00280.hp1 HG00558.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.-16+1211A>T | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 1/5 | chr1 | 53944344 | ||||||
chr1:53944415
|
CA | C | 6 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(3): Show | 6 | HG02280.hp2 HG02572.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.-16+1139delT | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 1/5 | chr1 | 53944415 | ||||||
chr1:53944517
|
T | C | 59 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(56): Show | 96 | HG00099.hp1 HG00280.hp1 HG00558.hp1 others(93): Show |
intron_variant | MODIFIER | c.-16+1038A>G | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 1/5 | chr1 | 53944517 | ||||||
chr1:53944787
|
T | A | 10 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(7): Show | 11 | HG01109.hp1 HG02280.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.-16+768A>T | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 1/5 | chr1 | 53944787 | ||||||
chr1:53944938
|
C | T | 1 | a0001c0001t0001g0037 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-16+617G>A | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 1/5 | chr1 | 53944938 | ||||||
chr1:53944982
|
T | C | 18 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0012others(15): Show | 39 | HG00280.hp1 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.-16+573A>G | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 1/5 | chr1 | 53944982 | ||||||
chr1:53945057
|
G | T | 1 | a0001c0001t0001g0036 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-16+498C>A | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 1/5 | chr1 | 53945057 | ||||||
chr1:53945066
|
A | C | 1 | a0001c0001t0001g0035 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.-16+489T>G | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 1/5 | chr1 | 53945066 | ||||||
chr1:53945176
|
T | C | 1 | a0001c0001t0001g0152 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.-16+379A>G | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 1/5 | chr1 | 53945176 | ||||||
chr1:53945240
|
C | T | 1 | a0001c0001t0001g0034 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.-16+315G>A | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 1/5 | chr1 | 53945240 |