Product Details

SNP ID: rs148114656
Assay Type: Functionally Tested
NCBI dbSNP Submissions: NA
Location: Chr.12:52424717 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: AGGTTTCCACCTCCAATGCTGCTGC[C/T]GCTTCCATAGCCACTGGAAAGAGTA
Phenotype: MIM: 609025
Polymorphism: C/T, Transition Substitution
Allele Nomenclature
Literature Links: KRT75 PubMed Links
Additional Information: For this assay, SNP(s) [rs298104] 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_004693.2	1478	Missense Mutation			NP_004684.2