Product Details

SNP ID

rs142492595

Assay Type

Functionally tested

NCBI dbSNP Submissions

17

Location

Chr.1:232805198 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TCACTGTCTTTTACCACTTATATCC[C/T]CAGCATTATCATCAATTGTCTTAAT

Phenotype

Polymorphism

C/T, 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	307	Missense Mutation	CCA,TCA	P59S	NP_061963.2

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