Product Details

SNP ID
rs201019085
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.2:118843028 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GGTGCAGCGCCAGGCCGTTCTTGAT[G/T]CCTGTGGCTTTCTTGATCTTGGCGC
Phenotype
MIM: 131290
Polymorphism
G/T, Transversion substitution
Allele Nomenclature
Literature Links
EN1 PubMed Links

Gene Details

Gene
EN1
Gene Name
engrailed homeobox 1
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001426.3 2105 Silent Mutation GGA,GGC G363G NP_001417.3

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