Product Details

SNP ID
rs140052190
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.X:43767514 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TTTTGTGGGCCAGGAAGCCAAGAGC[C/T]GTTGCTGAAAAGATGGTGGTCAATC
Phenotype
MIM: 309860
Polymorphism
C/T, Transition 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 1651 Silent Mutation ACA,ACG T505T NP_000889.3
XM_005272608.3 1651 Silent Mutation ACA,ACG T489T XP_005272665.1
XM_017029523.1 1651 Silent Mutation ACA,ACG T489T XP_016885012.1
XM_017029524.1 1651 Silent Mutation ACA,ACG T489T XP_016885013.1

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