Product Details

SNP ID: rs144660633
Assay Type: Functionally Tested
NCBI dbSNP Submissions: NA
Location: Chr.4:4862762 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: ACAAGACGAACCGTAAGCCGCGGAC[A/G]CCCTTCACCACCGCGCAGCTGCTGG
Phenotype: MIM: 142983
Polymorphism: A/G, Transition Substitution
Allele Nomenclature
Literature Links: MSX1 PubMed Links
Additional Information: For this assay, SNP(s) [rs1042484] 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_002448.3	766	Silent Mutation	ACA,ACG	T177T	NP_002439.2