Product Details

SNP ID
rs138007513
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.7:155462426 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
ACCCGAACAAAGAGGACAAGCGGCC[A/G]CGCACGGCCTTTACCGCCGAGCAGC
Phenotype
MIM: 131310
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
EN2 PubMed Links

Gene Details

Gene
EN2
Gene Name
engrailed homeobox 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001427.3 990 Silent Mutation CCA,CCG P247P NP_001418.2

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