Product Details

SNP ID
rs544908
Assay Type
Validated
NCBI dbSNP Submissions
NA
Location
Chr.5:154044038 on Build GRCh38
Set Membership
HapMap Validated
Context Sequence [VIC/FAM]
CTGTTGCATTCACAATATAATTACA[C/T]TTCAGTCACATTGTCTTAGATACAG
Phenotype
MIM: 600491
Polymorphism
C/T, Transition Substitution
Allele Nomenclature
Literature Links
FAM114A2 PubMed Links
Additional Information
For this assay, SNP(s) [rs115393578] 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

Gene
FAM114A2
Gene Name
family with sequence similarity 114 member A2
There are no transcripts associated with this gene.

Gene
MFAP3
Gene Name
microfibrillar associated protein 3
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001135037.1 Intron NP_001128509.1
NM_001242336.1 Intron NP_001229265.1
NM_005927.4 Intron NP_005918.1

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