Product Details

SNP ID: rs148293871
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.16:75207128 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: CAGGAGGGCCCAGCAGGAGAGGAGC[A/C]AGAGGAAAGCCATGGTGCCGCTGGC
Phenotype
Polymorphism: A/C, 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	47	Missense Mutation	TGG,TTG	W5L	NP_001020371.3