Product Details

SNP ID: rs200112350
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.16:75206129 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: GCCAGGGCCAGGAGCCGGGGACGGC[A/G]TCCTCCCCATTCACGATCCTGGACA
Phenotype
Polymorphism: A/G, Transition 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	150	Silent Mutation	GAC,GAT	D39D	NP_001020371.3