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NM_001005361.3(DNM2):c.1020T>G (p.Phe340Leu) AND not provided

Germline classification:
Uncertain significance (1 submission)
Last evaluated:
Jan 10, 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:
RCV003313666.1

Allele description [Variation Report for NM_001005361.3(DNM2):c.1020T>G (p.Phe340Leu)]

NM_001005361.3(DNM2):c.1020T>G (p.Phe340Leu)

Gene:
DNM2:dynamin 2 [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
19p13.2
Genomic location:
Preferred name:
NM_001005361.3(DNM2):c.1020T>G (p.Phe340Leu)
HGVS:
  • NC_000019.10:g.10793747T>G
  • NG_008792.1:g.80669T>G
  • NM_001005360.3:c.1020T>G
  • NM_001005361.3:c.1020T>GMANE SELECT
  • NM_001005362.3:c.1020T>G
  • NM_001190716.2:c.1020T>G
  • NM_004945.4:c.1020T>G
  • NP_001005360.1:p.Phe340Leu
  • NP_001005360.1:p.Phe340Leu
  • NP_001005361.1:p.Phe340Leu
  • NP_001005361.1:p.Phe340Leu
  • NP_001005362.1:p.Phe340Leu
  • NP_001177645.1:p.Phe340Leu
  • NP_004936.2:p.Phe340Leu
  • LRG_238t1:c.1020T>G
  • LRG_238t2:c.1020T>G
  • LRG_238:g.80669T>G
  • LRG_238p1:p.Phe340Leu
  • LRG_238p2:p.Phe340Leu
  • NC_000019.9:g.10904423T>G
  • NM_001005360.2:c.1020T>G
  • NM_001005361.2:c.1020T>G
Protein change:
F340L
Molecular consequence:
  • NM_001005360.3:c.1020T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001005361.3:c.1020T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001005362.3:c.1020T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001190716.2:c.1020T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_004945.4:c.1020T>G - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Synonyms:
none provided
Identifiers:
MedGen: CN517202

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Assertion and evidence details

Help
Submission AccessionSubmitterReview Status
(Assertion method)		Clinical Significance
(Last evaluated)		OriginMethodCitations
SCV004012726GeneDx
criteria provided, single submitter

(GeneDx Variant Classification Process June 2021)		Uncertain significance
(Jan 10, 2023) 		germlineclinical testing

Citation Link

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Summary from all submissions

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

Details of each submission

From GeneDx, SCV004012726.1

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

Description

Not observed at significant frequency in large population cohorts (gnomAD); Missense variants in this gene are often considered pathogenic (HGMD); In silico analysis supports that this missense variant has a deleterious effect on protein structure/function; Has not been previously published as pathogenic or benign to our knowledge; De novo variant with confirmed parentage in a patient referred for genetic testing at GeneDx; however, the reported clinical features are only partially consistent with the features typically observed in individuals with pathogenic variants in this gene; This variant is associated with the following publications: (PMID: 16227997)

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

Last Updated: Jul 22, 2023