Product Details

SNP ID: rs5760192
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.22:20721371 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: TCCAGATGAACTGGTGTGCCAGAAG[C/T]TGGGATTTAGACGCTGCCCACAGAA
Phenotype: MIM: 600286
Polymorphism: C/T, Transition substitution
Allele Nomenclature
Literature Links: PI4KA PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_058004.3	5130	Silent Mutation	CAA,CAG	Q1681Q	NP_477352.3