Product Details

SNP ID
rs3824067
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.7:155461246 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
GGGGCCAGATGCTCCCTAAAGCCGA[A/T]TCATACACCGCACAAATTGAAACCC
Phenotype
MIM: 131310
Polymorphism
A/T, Transversion 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 Intron NP_001418.2

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