Product Details

SNP ID

rs200799879

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.13:80337391 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CCGTGCTTATGGATCTGGACAGAGG[C/G]GCTCGTGCAGAAGAATGGACCTGCG

Phenotype

MIM: 602466

Polymorphism

C/G, Transversion Substitution

Allele Nomenclature

Literature Links

SPRY2 PubMed Links

Additional Information

For this assay, SNP(s) [rs504122] 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

SPRY2

Gene Name

sprouty RTK signaling antagonist 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001318536.1	860	Silent Mutation	GCC,GCG	A105A	NP_001305465.1
NM_001318537.1	860	Silent Mutation	GCC,GCG	A105A	NP_001305466.1
NM_001318538.1	860	Silent Mutation	GCC,GCG	A105A	NP_001305467.1
NM_005842.3	860	Silent Mutation	GCC,GCG	A105A	NP_005833.1

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