Product Details

SNP ID

rs4681774

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.3:58011875 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TGGGCATGTGTTGCTTAGAAAATGG[C/T]GCCTGTTAATTAAATAAGGTGCTGT

Phenotype

MIM: 603381

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

FLNB PubMed Links

Additional Information

For this assay, SNP(s) [rs115861088] 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

FLNB

Gene Name

filamin B

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001164317.1		Intron			NP_001157789.1
NM_001164318.1		Intron			NP_001157790.1
NM_001164319.1		Intron			NP_001157791.1
NM_001457.3		Intron			NP_001448.2
XM_005264978.1		Intron			XP_005265035.1

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