Product Details

SNP ID
rs12567597
Assay Type
Functionally tested
NCBI dbSNP Submissions
34
Location
Chr.1:232805608 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
GGGAGGCCTCGTCGCCGCGCGGTCT[G/T]TGCCCCGCCGTGGCCTTCCGCCTGC
Phenotype
Polymorphism
G/T, Transversion substitution
Allele Nomenclature
Literature Links
MAP10 PubMed Links

Gene Details

Gene
MAP10
Gene Name
microtubule associated protein 10
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_019090.2 717 Silent Mutation CTG,CTT L195L NP_061963.2

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