Product Details

SNP ID

rs202208990

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.4:176687380 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CTGGGGAAGAGTTTGTTTTTACAGA[A/C]ACACTGGCATGAGTTTCTGTCTAGT

Phenotype

MIM: 601528

Polymorphism

A/C, Transversion substitution

Allele Nomenclature

Literature Links

VEGFC PubMed Links

Gene Details

Gene

VEGFC

Gene Name

vascular endothelial growth factor C

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_005429.4	1386	Missense Mutation	GTC,TTC	V318F	NP_005420.1

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