Product Details

SNP ID

hCV25995988

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.12:110127771 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TTGGTTAGGGAATGAAAATTCTTTT[A/C]CAAAAGGTTTTATTGTATTGCAAGT

Phenotype

MIM: 605489

Polymorphism

A/C, Transversion 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		Intron			NP_001137251.1
NM_014055.3		Intron			NP_054774.2
NM_031473.3		Intron			NP_113661.2

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