Product Details

SNP ID: rs7613994
Assay Type: Validated
NCBI dbSNP Submissions: NA
Location: Chr.3:119181008 on Build GRCh38
Set Membership: HapMap Validated
Context Sequence [VIC/FAM]: ACACAGACTTTGTAAGGTCAGCTTA[A/C]ACGTTGTGACCAGTTTTTCAACATC
Phenotype: MIM: 602380
Polymorphism: A/C, Transversion Substitution
Allele Nomenclature
Literature Links: UPK1B PubMed Links
Additional Information: For this assay, SNP(s) [rs72955044] 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_006952.3		Intron			NP_008883.2