Product Details

SNP ID

rs4392721

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.6:43773464 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GGCGAGGGGAGGAATGATCTGATGC[A/G]GGTGGGGAGGGTTAGAGGAGGCCTC

Phenotype

MIM: 192240

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

VEGFA PubMed Links

Additional Information

For this assay, SNP(s) [rs76248721] are located under a probe 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

VEGFA

Gene Name

vascular endothelial growth factor A

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001025366.2		Intron			NP_001020537.2
NM_001025367.2		Intron			NP_001020538.2
NM_001025368.2		Intron			NP_001020539.2
NM_001025369.2		Intron			NP_001020540.2
NM_001025370.2		Intron			NP_001020541.2
NM_001033756.2		Intron			NP_001028928.1
NM_001171622.1		Intron			NP_001165093.1
NM_001171623.1		Intron			NP_001165094.1
NM_001171624.1		Intron			NP_001165095.1
NM_001171625.1		Intron			NP_001165096.1
NM_001171626.1		Intron			NP_001165097.1
NM_001171627.1		Intron			NP_001165098.1
NM_001171628.1		Intron			NP_001165099.1
NM_001171629.1		Intron			NP_001165100.1
NM_001171630.1		Intron			NP_001165101.1
NM_001204384.1		Intron			NP_001191313.1
NM_001204385.1		Intron			NP_001191314.1
NM_001287044.1		Intron			NP_001273973.1
NM_001317010.1		Intron			NP_001303939.1
NM_003376.5		Intron			NP_003367.4

View Full Product Details