NM_181723.3(MICU3):c.947G>A (p.Arg316His) AND not specified

Germline classification:: Uncertain significance (1 submission)
Last evaluated:: Jun 2, 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:: RCV004304973.1

Allele description [Variation Report for NM_181723.3(MICU3):c.947G>A (p.Arg316His)]

NM_181723.3(MICU3):c.947G>A (p.Arg316His)

Gene:

MICU3:mitochondrial calcium uptake family member 3 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

8p22

Genomic location:

Preferred name:

NM_181723.3(MICU3):c.947G>A (p.Arg316His)

HGVS:

NC_000008.11:g.17098516G>A
NM_001349810.2:c.929G>A
NM_001413217.1:c.908G>A
NM_001413218.1:c.889-5875G>A
NM_001413219.1:c.850-5875G>A
NM_001413221.1:c.419G>A
NM_001413222.1:c.761G>A
NM_001413223.1:c.899G>A
NM_001413224.1:c.888+7932G>A
NM_001413225.1:c.626G>A
NM_001413226.1:c.788G>A
NM_181723.3:c.947G>AMANE SELECT
NP_001336739.1:p.Arg310His
NP_001400146.1:p.Arg303His
NP_001400150.1:p.Arg140His
NP_001400151.1:p.Arg254His
NP_001400152.1:p.Arg300His
NP_001400154.1:p.Arg209His
NP_001400155.1:p.Arg263His
NP_859074.1:p.Arg316His
NC_000008.10:g.16956025G>A
NM_181723.2:c.947G>A
NR_146233.2:n.1176G>A
NR_182122.1:n.989G>A
NR_182123.1:n.1015G>A
NR_182124.1:n.1047G>A

Protein change:

R140H

Molecular consequence:

NM_001413218.1:c.889-5875G>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001413219.1:c.850-5875G>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001413224.1:c.888+7932G>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001349810.2:c.929G>A - missense variant - [Sequence Ontology: SO:0001583]
NM_001413217.1:c.908G>A - missense variant - [Sequence Ontology: SO:0001583]
NM_001413221.1:c.419G>A - missense variant - [Sequence Ontology: SO:0001583]
NM_001413222.1:c.761G>A - missense variant - [Sequence Ontology: SO:0001583]
NM_001413223.1:c.899G>A - missense variant - [Sequence Ontology: SO:0001583]
NM_001413225.1:c.626G>A - missense variant - [Sequence Ontology: SO:0001583]
NM_001413226.1:c.788G>A - missense variant - [Sequence Ontology: SO:0001583]
NM_181723.3:c.947G>A - missense variant - [Sequence Ontology: SO:0001583]
NR_146233.2:n.1176G>A - non-coding transcript variant - [Sequence Ontology: SO:0001619]
NR_182122.1:n.989G>A - non-coding transcript variant - [Sequence Ontology: SO:0001619]
NR_182123.1:n.1015G>A - non-coding transcript variant - [Sequence Ontology: SO:0001619]
NR_182124.1:n.1047G>A - non-coding transcript variant - [Sequence Ontology: SO:0001619]

Condition(s)

Synonyms:: AllHighlyPenetrant
Identifiers:: MedGen: CN169374

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV003963800	Ambry Genetics	criteria provided, single submitter (Ambry Variant Classification Scheme 2023)	Uncertain significance (Jun 2, 2023)	germline	clinical testing	Citation Link

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV003963800

Ambry Genetics

criteria provided, single submitter

(Ambry Variant Classification Scheme 2023)

Uncertain significance
(Jun 2, 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	unknown	not provided	not provided	not provided	not provided	not provided	clinical testing

Details of each submission

From Ambry Genetics, SCV003963800.2

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

Description

The c.947G>A (p.R316H) alteration is located in exon 9 (coding exon 9) of the MICU3 gene. This alteration results from a G to A substitution at nucleotide position 947, causing the arginine (R) at amino acid position 316 to be replaced by a histidine (H). Based on insufficient or conflicting evidence, the clinical significance of this alteration remains unclear.

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

Last Updated: Oct 26, 2024

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