Product Details

SNP ID
rs201361420
Assay Type
Functionally tested
NCBI dbSNP Submissions
11
Location
Chr.1:232805678 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GGTTTACCCTCCTGACGGCCCCGGC[A/G]CTCCCGCCGCCGAACCGTGGCCCGG
Phenotype
Polymorphism
A/G, Transition 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_019090.2 787 Missense Mutation ACT,GCT T219A NP_061963.2

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