Product Details

SNP ID: rs10034385
Assay Type: Functionally Tested
NCBI dbSNP Submissions: NA
Location: Chr.4:176684662 on Build GRCh38
Set Membership: HapMap
Context Sequence [VIC/FAM]: CCTCCCATCCTAGACTTCCAGTTTC[C/T]AGTAGCGGTGAGAGGACAAATTATC
Phenotype: MIM: 601528
Polymorphism: C/T, Transition Substitution
Allele Nomenclature
Literature Links: VEGFC PubMed Links
Additional Information: For this assay, SNP(s) [rs114475399] 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

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_005429.4		Intron			NP_005420.1