Product Details

SNP ID

hCV64446854

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.X:43766615 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CAAAAAGAAAGGACAGCAGATATGG[G/T]CAATCAACTTTTATTTTTAATTACC

Phenotype

MIM: 309860

Polymorphism

G/T, Transversion substitution

Allele Nomenclature

Literature Links

MAOB PubMed Links

Gene Details

Gene

MAOB

Gene Name

monoamine oxidase B

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_000898.4	2590	UTR 3			NP_000889.3

View Full Product Details