Product Details

SNP ID: rs146416678
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.5:52989528 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: CGCTGCTGCTGGTGTTAGCGCTCAG[C/T]CAAGGTAAGCGGGGATTTCGCTCTG
Phenotype: MIM: 192974
Polymorphism: C/T, 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	203	Silent Mutation	AGC,AGT	S20S	NP_002194.2