Product Details

SNP ID: rs7922366
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.10:97649508 on Build GRCh38
Set Membership: HapMap
Context Sequence [VIC/FAM]: AGCTTCATTCTAACCAAGTAGCAGA[A/G]TCTTTTTCCTGCTGTGATTTTTCTC
Phenotype: MIM: 609763
Polymorphism: A/G, Transition substitution
Allele Nomenclature
Literature Links: PI4K2A PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_018425.3		Intron			NP_060895.1