Product Details

SNP ID

rs10112249

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.8:81441268 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

CAAGAGGTTGTCCATTTTTTTCCAT[C/T]GCATGGTTACTATTCTTTCCCCAGA

Phenotype

MIM: 170715

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

PMP2 PubMed Links

Gene Details

Gene

PMP2

Gene Name

peripheral myelin protein 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_002677.3	2627	UTR 3			NP_002668.1

View Full Product Details