Product Details

SNP ID
rs16831157
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.3:160268497 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
ACTTTTGACGGTAAGCAAGAACTGT[A/G]TCAACATGTGTTTTGTATTTTACAG
Phenotype
MIM: 611177
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
IFT80 PubMed Links

Gene Details

Gene
IFT80
Gene Name
intraflagellar transport 80
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001190241.1 2572 Silent Mutation GAC,GAT D576D NP_001177170.1
NM_001190242.1 2572 Silent Mutation GAC,GAT D576D NP_001177171.1
NM_020800.2 2572 Silent Mutation GAC,GAT D713D NP_065851.1

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