Product Details

SNP ID: rs199273
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.3:37452470 on Build GRCh38
Set Membership: HapMap
Context Sequence [VIC/FAM]: GGATCCCCGCGGGCGCCTACAACCT[C/T]GACCCGCAGCGCCCCGTGCACTTCC
Phenotype: MIM: 603963
Polymorphism: C/T, Transition substitution
Allele Nomenclature
Literature Links: ITGA9 PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_002207.2	149	Silent Mutation	CTC,CTT	L32L	NP_002198.2