Product Details

SNP ID: rs77879475
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.5:71719387 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: GGGTACCCGTGCCCAGGAGGACGCC[A/G]AGCTCCAGCCCCGAGCCCTGGACAT
Phenotype: MIM: 602606
Polymorphism: A/G, Transition substitution
Allele Nomenclature
Literature Links: CARTPT PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_004291.3	225	Missense Mutation	AAG,GAG	K32E	NP_004282.1