Product Details

SNP ID: rs12276274
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.11:104887434 on Build GRCh38
Set Membership: HapMap
Context Sequence [VIC/FAM]: TGGAGAAGAGAGGGAAACCAATGCT[A/G]AATAAAGATGGACCTCCAACTTCCA
Phenotype: MIM: 608633
Polymorphism: A/G, Transition substitution
Allele Nomenclature
Literature Links: CASP12 PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001191016.2		Intron			NP_001177945.2