Product Details

SNP ID

rs35279564

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.7:128835777 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

ACCTGATGAGTGTGCCAGATTCCGC[A/G]GAGGCAGGAAGAGGTTTAAAACCCC

Phenotype

MIM: 102565

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

FLNC PubMed Links

Additional Information

For this assay, SNP(s) [rs74448849] 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

FLNC

Gene Name

filamin C

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001127487.1		Intron			NP_001120959.1
NM_001458.4		Intron			NP_001449.3

View Full Product Details