Product Details

SNP ID: rs970348
Assay Type: Functionally Tested
NCBI dbSNP Submissions: NA
Location: Chr.14:22600948 on Build GRCh38
Set Membership: HapMap
Context Sequence [VIC/FAM]: GGTCCCTGGGTATGAAGGAGAAAAC[A/G]GGATGAGTTATCTGTGTTACCGCAT
Phenotype
Polymorphism: A/G, Transition Substitution
Allele Nomenclature
Literature Links: ABHD4 PubMed Links
Additional Information: For this assay, SNP(s) [rs61972419] 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_022060.2		Intron			NP_071343.2
XM_005267986.4		Intron			XP_005268043.1