Product Details

SNP ID: rs1049299
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.16:75204232 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: ACACGGGCGTACACAGCGGGCGTGG[A/T]GGTAGAGCAGGTGCGGCTGCCCCAG
Phenotype
Polymorphism: A/T, Transversion substitution
Allele Nomenclature
Literature Links: CTRB2 PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001025200.3	754	Missense Mutation	ACC,TCC	T241S	NP_001020371.3