Product Details

SNP ID: rs9494888
Assay Type: Functionally Tested
NCBI dbSNP Submissions: NA
Location: Chr.6:99613722 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: TCACCACCACGCGCACCACCACCAC[A/C]ATCCCAAGTGCCTGCTCGCTGGGGA
Phenotype: MIM: 616741
Polymorphism: A/C, Transversion Substitution
Allele Nomenclature
Literature Links: PRDM13 PubMed Links
Additional Information: For this assay, SNP(s) [rs577768379] 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_021620.3	1348	Missense Mutation	AAT,CAT	N363H	NP_067633.2