Product Details

SNP ID
rs140262266
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.X:43767598 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
AATGTCTCTCCAAAAAGGTGGTGGT[A/G]ATGGGCTGTGCAGGGACATCCTAGG
Phenotype
MIM: 309860
Polymorphism
A/G, 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 1567 Silent Mutation ATC,ATT I477I NP_000889.3
XM_005272608.3 1567 Silent Mutation ATC,ATT I461I XP_005272665.1
XM_017029523.1 1567 Silent Mutation ATC,ATT I461I XP_016885012.1
XM_017029524.1 1567 Silent Mutation ATC,ATT I461I XP_016885013.1

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