Product Details

SNP ID: rs181052688
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.8:70644067 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: AAAAAAATTTAAAAATTACCCACCT[A/G]GATATATAATATCAGCTTTGATTTT
Phenotype
Polymorphism: A/G, Transition substitution
Allele Nomenclature
Literature Links: LACTB2 PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_016027.2	682	Missense Mutation	CCA,CTA	P197L	NP_057111.1

There are no transcripts associated with this gene.