NM_001005361.3(DNM2):c.1218C>T (p.Asp406=) AND not specified

Germline classification:: Benign (2 submissions)
Last evaluated:: Aug 22, 2016
Review status:: 2 stars out of maximum of 4 stars
criteria provided, multiple submitters, no conflicts

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:: RCV000429576.13

Allele description [Variation Report for NM_001005361.3(DNM2):c.1218C>T (p.Asp406=)]

NM_001005361.3(DNM2):c.1218C>T (p.Asp406=)

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.1218C>T (p.Asp406=)

HGVS:

NC_000019.10:g.10797401C>T
NG_008792.1:g.84323C>T
NM_001005360.3:c.1336-1085C>T
NM_001005361.3:c.1218C>TMANE SELECT
NM_001005362.3:c.1218C>T
NM_001190716.2:c.1336-1085C>T
NM_004945.4:c.1336-1085C>T
NP_001005361.1:p.Asp406=
NP_001005361.1:p.Asp406=
NP_001005362.1:p.Asp406=
LRG_238t1:c.1336-1085C>T
LRG_238t2:c.1218C>T
LRG_238:g.84323C>T
LRG_238p2:p.Asp406=
NC_000019.9:g.10908077C>T
NM_001005360.2:c.1336-1085C>T
NM_001005361.2:c.1218C>T
p.Asp406Asp

Links:

dbSNP: rs147668465

NCBI 1000 Genomes Browser:

rs147668465

Molecular consequence:

NM_001005360.3:c.1336-1085C>T - intron variant - [Sequence Ontology: SO:0001627]
NM_001190716.2:c.1336-1085C>T - intron variant - [Sequence Ontology: SO:0001627]
NM_004945.4:c.1336-1085C>T - intron variant - [Sequence Ontology: SO:0001627]
NM_001005361.3:c.1218C>T - synonymous variant - [Sequence Ontology: SO:0001819]
NM_001005362.3:c.1218C>T - synonymous variant - [Sequence Ontology: SO:0001819]

Observations:

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
SCV000522790	GeneDx	criteria provided, single submitter (GeneDx Variant Classification (06012015))	Benign (Jan 30, 2016)	germline	clinical testing	Citation Link,
SCV000711575	Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine	criteria provided, single submitter (LMM Criteria)	Benign (Aug 22, 2016)	germline	clinical testing	PubMed (1) [See all records that cite this PMID]

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV000522790

GeneDx

criteria provided, single submitter

(GeneDx Variant Classification (06012015))

Benign
(Jan 30, 2016)

germline

clinical testing

Citation Link,

SCV000711575

Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine

criteria provided, single submitter

(LMM Criteria)

Benign
(Aug 22, 2016)

germline

clinical testing

PubMed (1)
[See all records that cite this PMID]

Help

Summary from all submissions

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

Citations

PubMed

A systematic approach to assessing the clinical significance of genetic variants.

Duzkale H, Shen J, McLaughlin H, Alfares A, Kelly MA, Pugh TJ, Funke BH, Rehm HL, Lebo MS.

Clin Genet. 2013 Nov;84(5):453-63. doi: 10.1111/cge.12257.

PubMed [citation]

PMID:: 24033266
PMCID:: PMC3995020

Details of each submission

From GeneDx, SCV000522790.4

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

Description

This variant is considered likely benign or benign based on one or more of the following criteria: it is a conservative change, it occurs at a poorly conserved position in the protein, it is predicted to be benign by multiple in silico algorithms, and/or has population frequency not consistent with disease.

#	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		not provided	not provided	not provided	not provided

From Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine, SCV000711575.1

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

Description

p. Asp406Asp in exon 10B of DNM2: This variant is not expected to have clinical significance because it does not alter an amino acid residue and is not located within the splice consensus sequence. It has been identified in 0.6% (106/16350) of South Asian chromosomes, including 1 homozygote by the Exome Aggregation Con sortium (ExAC, http://exac.broadinstitute.org; dbSNP rs147668465).

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

Last Updated: Apr 15, 2024

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