Product Details

SNP ID

rs6324

Assay Type

DME

NCBI dbSNP Submissions

NA

Location

Chr.X:43767568 on Build GRCh38

Set Membership

HapMap DME Validated Inventoried

Context Sequence [VIC/FAM]

TCAGCCTGAGCAGGCCTGGCACGGA[A/G]GGCAAATGTCTCTCCAAAAAGGTGG

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	1597	Silent Mutation	CCC,CCT	P487P	NP_000889.3
XM_005272608.3	1597	Silent Mutation	CCC,CCT	P471P	XP_005272665.1
XM_017029523.1	1597	Silent Mutation	CCC,CCT	P471P	XP_016885012.1
XM_017029524.1	1597	Silent Mutation	CCC,CCT	P471P	XP_016885013.1

View Full Product Details