Product Details

SNP ID

rs6479442

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.9:92953435 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

AGTTTGAAGCTGGGCTTGCCTCTCC[A/C]CTTTGGCCAAGATGACTAAAGCATC

Phenotype

Polymorphism

A/C, Transversion Substitution

Allele Nomenclature

Literature Links

FGD3 PubMed Links

Additional Information

For this assay, SNP(s) [rs77156202] 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

FGD3

Gene Name

FYVE, RhoGEF and PH domain containing 3

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001083536.1		Intron			NP_001077005.1
NM_001286993.1		Intron			NP_001273922.1
NM_033086.2		Intron			NP_149077.2
XM_017015274.1		Intron			XP_016870763.1

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