Product Details

SNP ID: rs13130130
Assay Type: Functionally Tested
NCBI dbSNP Submissions: NA
Location: Chr.4:109568078 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: GTAATGTGACCATAAACCTGGGGGG[A/G]AAAAATTATTTTAGAGAGTGTTTTG
Phenotype
Polymorphism: A/G, Transition Substitution
Allele Nomenclature
Literature Links: MCUB PubMed Links
Additional Information: For this assay, SNP(s) [rs112079518,rs113970980] 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_017918.4		Intron			NP_060388.2
XM_006714246.3		Intron			XP_006714309.1