NM_000898.5(MAOB):c.1431C>T (p.Ile477=) AND not provided

Germline classification:: Likely benign (1 submission)
Last evaluated:: Feb 1, 2023
Review status:: 1 star out of maximum of 4 stars
criteria provided, single submitter

Somatic classification of clinical impact:: None
Review status:: (0/4) 0 stars out of maximum of 4 stars
no assertion criteria provided

Somatic classification of oncogenicity:: None
Review status:: (0/4) 0 stars out of maximum of 4 stars
no assertion criteria provided

Record status:: current
Accession:: RCV003438133.10

Allele description [Variation Report for NM_000898.5(MAOB):c.1431C>T (p.Ile477=)]

NM_000898.5(MAOB):c.1431C>T (p.Ile477=)

Gene:

MAOB:monoamine oxidase B [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

Xp11.3

Genomic location:

Preferred name:

NM_000898.5(MAOB):c.1431C>T (p.Ile477=)

HGVS:

NC_000023.11:g.43767598G>A
NG_008723.2:g.119878C>T
NM_000898.5:c.1431C>TMANE SELECT
NP_000889.3:p.Ile477=
NC_000023.10:g.43626845G>A

Molecular consequence:

NM_000898.5:c.1431C>T - synonymous variant - [Sequence Ontology: SO:0001819]

Observations:

Condition(s)

Synonyms:: none provided
Identifiers:: MedGen: C3661900

Recent activity

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PREDICTED: Rattus norvegicus exocyst complex component 1 (Exoc1), transcript var...
PREDICTED: Rattus norvegicus exocyst complex component 1 (Exoc1), transcript variant X6, mRNA
gi|2678894914|ref|XM_063273077.1|

Nucleotide
Arabidopsis thaliana Flavin-binding monooxygenase family protein (AT1G12160), mR...
Arabidopsis thaliana Flavin-binding monooxygenase family protein (AT1G12160), mRNA
gi|1063682759|ref|NM_101088.4|

Nucleotide
PD_0153
PD_0153

biosample
MIGS Eukaryotic sample from Eulemur macaco
MIGS Eukaryotic sample from Eulemur macaco

biosample
Pulmonary Edema
Pulmonary Edema
Excessive accumulation of extravascular fluid in the lung, an indication of a serious underlying disease or disorder. Pulmonary edema prevents efficient PULMONARY GAS EXCHANGE...<br/>Year introduced: WET LUNG was see RESPIRATORY DISTRESS SYNDROME, ADULT 1977-1991

MeSH

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV004164912	CeGaT Center for Human Genetics Tuebingen	criteria provided, single submitter (CeGaT Center For Human Genetics Tuebingen Variant Classification Criteria Version 2)	Likely benign (Feb 1, 2023)	germline	clinical testing	Citation Link

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV004164912

CeGaT Center for Human Genetics Tuebingen

criteria provided, single submitter

(CeGaT Center For Human Genetics Tuebingen Variant Classification Criteria Version 2)

Likely benign
(Feb 1, 2023)

germline

clinical testing

Citation Link

Help

Summary from all submissions

Ethnicity	Origin	Affected	Individuals	Families	Chromosomes tested	Number Tested	Family history	Method
not provided	germline	yes	1	not provided	not provided	not provided	not provided	clinical testing

Details of each submission

From CeGaT Center for Human Genetics Tuebingen, SCV004164912.10

#	Ethnicity	Individuals	Chromosomes Tested	Family History	Method	Citations
1	not provided	1	not provided	not provided	clinical testing	not provided

Description

MAOB: BP4, BP7, BS2

#	Sample				Method		Observation
#	Origin	Affected	Number tested	Tissue	Purpose	Method	Individuals	Allele frequency	Families	Co-occurrences
1	germline	yes	not provided	not provided	not provided		1	not provided	not provided	not provided

Last Updated: Oct 20, 2024

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