Product Details

SNP ID: rs2228601
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.19:19219049 on Build GRCh38
Set Membership: HapMap
Context Sequence [VIC/FAM]: TACCCTGCAGCCACGGCCAAGCGCA[A/G]CCCGAGATGCCCCTCGGATAAAGTG
Phenotype: MIM: 600826
Polymorphism: A/G, Transition substitution
Allele Nomenclature
Literature Links: NCAN PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_004386.2	307	Missense Mutation	ACC,GCC	T70A	NP_004377.2