Product Details

SNP ID
rs202166263
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.13:80337414 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GGGGCTCGTGCAGAAGAATGGACCT[G/T]CGAGTGCTGGAGCCTAGGAGGCTGG
Phenotype
MIM: 602466
Polymorphism
G/T, Transversion substitution
Allele Nomenclature
Literature Links
SPRY2 PubMed Links

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_001318536.1 837 Missense Mutation AAG,CAG K98Q NP_001305465.1
NM_001318537.1 837 Missense Mutation AAG,CAG K98Q NP_001305466.1
NM_001318538.1 837 Missense Mutation AAG,CAG K98Q NP_001305467.1
NM_005842.3 837 Missense Mutation AAG,CAG K98Q NP_005833.1

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