Product Details

SNP ID
rs149321431
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.17:41567625 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TCCTCCCCTGGACCCACTTCCTCCA[A/C]CATAGCCACCTCCACTTCCTCCTCC
Phenotype
MIM: 607606
Polymorphism
A/C, Transversion Substitution
Allele Nomenclature
Literature Links
KRT9 PubMed Links
Additional Information
For this assay, SNP(s) [rs3890472] are located under a primer 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

Gene
KRT9
Gene Name
keratin 9
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_000226.3 1586 Missense Mutation GGT,GTT G507V NP_000217.2

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