Product Details

SNP ID: rs186118079
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.X:76429338 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: CCTGAGAGACTGTGAGAGCCCCAAC[A/T]CCATTAGTATTATGGGCCTCAATAC
Phenotype: MIM: 300759
Polymorphism: A/T, Transversion substitution
Allele Nomenclature
Literature Links: MAGEE1 PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_020932.2	1686	Missense Mutation	ACC,TCC	T470S	NP_065983.1