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SNP ID: rs189410619
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.17:42851505 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: CCAGTGCCCAGCCTTGGACACACCC[C/T]GGCCAGAGCCAGCTGTTTGCAGACC
Phenotype: MIM: 602268 MIM: 603735 MIM: 605129
Polymorphism: C/T, Transition substitution
Allele Nomenclature
Literature Links: AOC2 PubMed Links

Gene Details

Gene: AOC2
Gene Name: amine oxidase, copper containing 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001158.3	383	Intron			NP_001149.2
NM_009590.2	383	Intron			NP_033720.2

Gene: AOC3
Gene Name: amine oxidase, copper containing 3

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001277731.1	383	Silent Mutation	CCC,CCT	P54P	NP_001264660.1
NM_001277732.1	383	Intron			NP_001264661.1
NM_003734.3	383	Silent Mutation	CCC,CCT	P54P	NP_003725.1
XM_011525419.1	383	Silent Mutation	CCC,CCT	P54P	XP_011523721.1
XM_011525420.2	383	Silent Mutation	CCC,CCT	P54P	XP_011523722.1

Gene: PSME3
Gene Name: proteasome activator subunit 3

There are no transcripts associated with this gene.

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