Product Details

SNP ID
rs145066542
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.22:36758362 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CCTTCTCCCGGTACAGCTGGTGGAA[C/T]TGCTTGGCAAGGCAGTGGAAAGGGG
Phenotype
MIM: 615870
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
IFT27 PubMed Links

Gene Details

Gene
IFT27
Gene Name
intraflagellar transport 27
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001177701.2 940 Silent Mutation CAA,CAG Q170Q NP_001171172.1
NM_006860.4 940 Silent Mutation CAA,CAG Q169Q NP_006851.1
XM_006724106.2 940 Silent Mutation CAA,CAG Q170Q XP_006724169.1
XM_017028540.1 940 Silent Mutation CAA,CAG Q129Q XP_016884029.1
Gene
LOC105373021
Gene Name
uncharacterized LOC105373021
There are no transcripts associated with this gene.

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