Product Details

SNP ID: rs3213641
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.7:25226804 on Build GRCh38
Set Membership: HapMap
Context Sequence [VIC/FAM]: TGGGGCAGGTTAGGAACACGTCTCA[C/T]GAGGCTCACCTCCATATTTCTTCCA
Phenotype: MIM: 616984
Polymorphism: C/T, Transition substitution
Allele Nomenclature
Literature Links: NPVF PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_022150.3	408	Missense Mutation	ATG,GTG	M121V	NP_071433.3