Product Details

SNP ID

rs2279622

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.5:180601743 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

GACACGCCAGTCCCACGTTGGACGA[C/T]GTGCAGAGGAAGGGGGAGGTCCACG

Phenotype

MIM: 136352

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

FLT4 PubMed Links

Additional Information

For this assay, SNP(s) [rs80139920] 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

FLT4

Gene Name

fms related tyrosine kinase 4

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_002020.4	6077	Intron			NP_002011.2
NM_182925.4	6077	UTR 3			NP_891555.2
XM_011534478.2	6077	UTR 3			XP_011532780.1
XM_011534484.2	6077	UTR 3			XP_011532786.1
XM_017009263.1	6077	UTR 3			XP_016864752.1
XM_017009264.1	6077	Intron			XP_016864753.1
XM_017009265.1	6077	Intron			XP_016864754.1
XM_017009266.1	6077	Intron			XP_016864755.1
XM_017009267.1	6077	Intron			XP_016864756.1
XM_017009268.1	6077	UTR 3			XP_016864757.1

View Full Product Details