Product Details

SNP ID: rs2494264
Assay Type: Functionally tested
NCBI dbSNP Submissions: 38
Location: Chr.1:159297048 on Build GRCh38
Set Membership: HapMap
Context Sequence [VIC/FAM]: CTCTCATCCTTGTCTGTTAACGGCC[A/T]AAAAGGATTCCTTTAAGAGATTTCT
Phenotype: MIM: 147140
Polymorphism: A/T, Transversion substitution
Allele Nomenclature
Literature Links: FCER1A PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_002001.3		Intron			NP_001992.1