Product Details

SNP ID

rs2733703

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.12:32408860 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GATGACCTGAGATATCTTGATTTTC[C/T]TACCTCATTGGTTCTTCAACTTTCT

Phenotype

MIM: 611104

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

FGD4 PubMed Links

Additional Information

For this assay, SNP(s) [rs77850101] 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

FGD4

Gene Name

FYVE, RhoGEF and PH domain containing 4

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001304480.1		Intron			NP_001291409.1
NM_001304481.1		Intron			NP_001291410.1
NM_001304483.1		Intron			NP_001291412.1
NM_001304484.1		Intron			NP_001291413.1
NM_139241.3		Intron			NP_640334.2
XM_005253304.4		Intron			XP_005253361.1
XM_005253307.3		Intron			XP_005253364.1
XM_005253308.4		Intron			XP_005253365.1
XM_005253309.1		Intron			XP_005253366.1
XM_005253310.3		Intron			XP_005253367.1
XM_011520554.1		Intron			XP_011518856.1
XM_011520555.1		Intron			XP_011518857.1
XM_011520556.1		Intron			XP_011518858.1
XM_011520557.1		Intron			XP_011518859.1
XM_011520558.2		Intron			XP_011518860.1
XM_011520559.2		Intron			XP_011518861.1
XM_017018803.1		Intron			XP_016874292.1
XM_017018804.1		Intron			XP_016874293.1
XM_017018805.1		Intron			XP_016874294.1

View Full Product Details