Product Details

SNP ID: rs150228591
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.14:75279895 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: GTTCTAGGACTTCTGCACGGACCTG[A/G]CCGTCTCCAGTGCCAACTTCATTCC
Phenotype: MIM: 164810
Polymorphism: A/G, Transition substitution
Allele Nomenclature
Literature Links: FOS PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_005252.3	365	Missense Mutation	ACC,GCC	T54A	NP_005243.1