Product Details

SNP ID
rs150531803
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.12:110128956 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
ATGTGTGTTTCTCTCTTAGGAGTAC[C/T]TTTCGTCAGGGTTTGGTGATTGGAA
Phenotype
MIM: 605489
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
IFT81 PubMed Links

Gene Details

Gene
IFT81
Gene Name
intraflagellar transport 81
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001143779.1 495 Silent Mutation ACC,ACT T85T NP_001137251.1
NM_014055.3 495 Silent Mutation ACC,ACT T85T NP_054774.2
NM_031473.3 495 Silent Mutation ACC,ACT T85T NP_113661.2
XM_011538232.2 495 Silent Mutation ACC,ACT T85T XP_011536534.1
XM_017019217.1 495 Silent Mutation ACC,ACT T85T XP_016874706.1
XM_017019218.1 495 UTR 5 XP_016874707.1

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