Product Details

SNP ID
rs79066821
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.13:80336864 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
AGGCCTGTTAACCCGGTCATAACAC[A/C]CCTGGCACAATTTAAGGCAACCCTT
Phenotype
MIM: 602466
Polymorphism
A/C, 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 1387 Missense Mutation NP_001305465.1
NM_001318537.1 1387 Missense Mutation NP_001305466.1
NM_001318538.1 1387 Missense Mutation NP_001305467.1
NM_005842.3 1387 Missense Mutation NP_005833.1

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