Product Details

SNP ID: rs77017418
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.19:29610532 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: CAAGGCGGTGGTCCTGGAGTACTTC[A/C]CCCGCCACAAGCGCAAGGAGAAGAA
Phenotype: MIM: 606114
Polymorphism: A/C, Transversion substitution
Allele Nomenclature
Literature Links: POP4 PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_006627.2	240	Missense Mutation	ACC,CCC	T62P	NP_006618.1