Product Details

SNP ID: rs26682
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.5:52993936 on Build GRCh38
Set Membership: HapMap
Context Sequence [VIC/FAM]: TTGGCAAGTGAAAGAAATGGAAGGT[G/T]GGTGGAGTTCTTTTTTTCCAGTTGT
Phenotype: MIM: 192974
Polymorphism: G/T, Transversion 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