Product Details

SNP ID: rs10065679
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.5:52993582 on Build GRCh38
Set Membership: HapMap
Context Sequence [VIC/FAM]: CGGCTGTGTCAGTTAAATTCCTTCC[A/G]AAGTGGATGATGACTACTCCCTGTC
Phenotype: MIM: 192974
Polymorphism: A/G, Transition substitution
Allele Nomenclature
Literature Links: ITGA2 PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_002203.3		Intron			NP_002194.2