Product Details

SNP ID: rs11868927
Assay Type: Validated
NCBI dbSNP Submissions: NA
Location: Chr.17:40959552 on Build GRCh38
Set Membership: Validated
Context Sequence [VIC/FAM]: TATGATCACAGCTCCTAAAGGTGAC[A/G]GCATTGATGACCATTGTGCTCACAT
Phenotype: MIM: 616678
Polymorphism: A/G, Transition Substitution
Allele Nomenclature
Literature Links: KRT39 PubMed Links
Additional Information: For this assay, SNP(s) [rs138086132] 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

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_213656.3		Intron			NP_998821.3