Product Details

SNP ID: rs13477828
Assay Type: Pre Designed
NCBI dbSNP Submissions: NA
Location: Chr.4:88196852 on Build GRCm38
Set Membership
Context Sequence [VIC/FAM]: TGACGTCATTGGAGAAGAGTCTGCC[A/G]CTAGTGACTGGCTGGCTACAGTGGA
Phenotype
Polymorphism: A/G, Transition substitution
Allele Nomenclature
Literature Links: Focad PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001081184.1	1369	Missense Mutation			NP_001074653.1