Product Details

SNP ID: rs148798647
Assay Type: Functionally Tested
NCBI dbSNP Submissions: NA
Location: Chr.16:89179544 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: TCCCCCCGATCAGCGTATCCGAGAA[C/T]CACAAGCGTCTCCCCTACCCCCTGG
Phenotype: MIM: 114019
Polymorphism: C/T, Transition Substitution
Allele Nomenclature
Literature Links: CDH15 PubMed Links
Additional Information: For this assay, SNP(s) [rs2287358] are located under a probe sequence. To help evaluate the possible impact of a given SNP on your experiment, please refer to the 1000 Genomes and NCBI dbSNP databases. A higher minor allele frequency in your study population represents a higher risk to assay performance.

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_004933.2	248	Silent Mutation	AAC,AAT	N57N	NP_004924.1