Product Details

SNP ID
rs2233069
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.15:23644697 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GCCCTCTCATCCAAGGGAGACAAGG[A/G]CTGTGCCTCCACCTTGGAATTATCC
Phenotype
MIM: 605283
Polymorphism
A/G, Transition Substitution
Allele Nomenclature
Literature Links
MAGEL2 PubMed Links

Gene Details

Gene
MAGEL2
Gene Name
MAGE family member L2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_019066.4 3150 Missense Mutation CCC,TCC P1016S NP_061939.3

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