Product Details

SNP ID: rs149857832
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.17:42844664 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: ATAGTCCTGGCGTTCCTGGCACTGT[C/T]CCTCATTACCATCTTTGCCCTGGCC
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	73	Missense Mutation	TCC,TTC	S13F	NP_001149.2
NM_009590.2	73	Missense Mutation	TCC,TTC	S13F	NP_033720.2

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

There are no transcripts associated with this gene.

Gene: PSME3
Gene Name: proteasome activator subunit 3

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001267045.1	73	Intron			NP_001253974.1
NM_005789.3	73	Intron			NP_005780.2
NM_176863.2	73	Intron			NP_789839.1
XM_011524177.2	73	Intron			XP_011522479.1

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