Product Details

SNP ID

rs9470452

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.6:37007348 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

CTGGGTGATTCTCCCCTGCCTCTCC[C/T]GGGATCTTTGCCAAGCTCGTCCTGT

Phenotype

MIM: 605091

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

FGD2 PubMed Links

Gene Details

Gene

FGD2

Gene Name

FYVE, RhoGEF and PH domain containing 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_173558.3		Intron			NP_775829.2
XM_011514372.2		Intron			XP_011512674.1
XM_011514373.2		Intron			XP_011512675.1
XM_017010429.1		Intron			XP_016865918.1

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