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NM_004294.4(MTRF1):c.248G>A (p.Ser83Asn) AND not specified

Germline classification:
Likely benign (1 submission)
Last evaluated:
May 17, 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:
RCV004286108.1

Allele description [Variation Report for NM_004294.4(MTRF1):c.248G>A (p.Ser83Asn)]

NM_004294.4(MTRF1):c.248G>A (p.Ser83Asn)

Gene:
MTRF1:mitochondrial translation release factor 1 [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
13q14.11
Genomic location:
Preferred name:
NM_004294.4(MTRF1):c.248G>A (p.Ser83Asn)
HGVS:
  • NC_000013.11:g.41260660C>T
  • NM_001354073.1:c.248G>A
  • NM_001354074.1:c.248G>A
  • NM_001354075.1:c.248G>A
  • NM_001354076.1:c.248G>A
  • NM_004294.4:c.248G>AMANE SELECT
  • NP_001341002.1:p.Ser83Asn
  • NP_001341003.1:p.Ser83Asn
  • NP_001341004.1:p.Ser83Asn
  • NP_001341005.1:p.Ser83Asn
  • NP_004285.2:p.Ser83Asn
  • NC_000013.10:g.41834796C>T
  • NM_004294.2:c.248G>A
Protein change:
S83N
Molecular consequence:
  • NM_001354073.1:c.248G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001354074.1:c.248G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001354075.1:c.248G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001354076.1:c.248G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_004294.4:c.248G>A - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Synonyms:
AllHighlyPenetrant
Identifiers:
MedGen: CN169374

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Assertion and evidence details

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Submission AccessionSubmitterReview Status
(Assertion method)		Clinical Significance
(Last evaluated)		OriginMethodCitations
SCV003938258Ambry Genetics
criteria provided, single submitter

(Ambry Variant Classification Scheme 2023)		Likely benign
(May 17, 2023) 		germlineclinical testing

Citation Link

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Summary from all submissions

EthnicityOriginAffectedIndividualsFamiliesChromosomes testedNumber TestedFamily historyMethod
not providedgermlineunknownnot providednot providednot providednot providednot providedclinical testing

Details of each submission

From Ambry Genetics, SCV003938258.2

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not providednot providednot providednot providedclinical testingnot provided

Description

This alteration is classified as likely benign based on a combination of the following: seen in unaffected individuals, population frequency, intact protein function, lack of segregation with disease, co-occurrence, RNA analysis, in silico models, amino acid conservation, lack of disease association in case-control studies, and/or the mechanism of disease or impacted region is inconsistent with a known cause of pathogenicity.

#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1germlineunknownnot providednot providednot providednot providednot providednot providednot provided

Last Updated: Oct 26, 2024