NM_004082.5(DCTN1):c.3010C>G (p.Leu1004Val) AND Inborn genetic diseases

Germline classification:: Likely benign (1 submission)
Last evaluated:: Jan 2, 2024
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:: RCV002438188.2

Allele description [Variation Report for NM_004082.5(DCTN1):c.3010C>G (p.Leu1004Val)]

NM_004082.5(DCTN1):c.3010C>G (p.Leu1004Val)

Gene:

DCTN1:dynactin subunit 1 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

2p13.1

Genomic location:

Preferred name:

NM_004082.5(DCTN1):c.3010C>G (p.Leu1004Val)

HGVS:

NC_000002.12:g.74365534G>C
NG_008735.2:g.31554C>G
NM_001135040.3:c.2950C>G
NM_001135041.3:c.2608C>G
NM_001190836.2:c.2899C>G
NM_001190837.2:c.2989C>G
NM_001378991.1:c.2959C>G
NM_001378992.1:c.2941C>G
NM_004082.5:c.3010C>GMANE SELECT
NM_023019.4:c.2608C>G
NP_001128512.1:p.Leu984Val
NP_001128513.1:p.Leu870Val
NP_001177765.1:p.Leu967Val
NP_001177766.1:p.Leu997Val
NP_001365920.1:p.Leu987Val
NP_001365921.1:p.Leu981Val
NP_004073.2:p.Leu1004Val
NP_004073.2:p.Leu1004Val
NP_075408.1:p.Leu870Val
LRG_237t1:c.3010C>G
LRG_237:g.31554C>G
LRG_237p1:p.Leu1004Val
NC_000002.11:g.74592661G>C
NM_004082.4:c.3010C>G
NR_033935.2:n.3073C>G

Protein change:

L1004V

Links:

dbSNP: rs758387062

NCBI 1000 Genomes Browser:

rs758387062

Molecular consequence:

NM_001135040.3:c.2950C>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001135041.3:c.2608C>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001190836.2:c.2899C>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001190837.2:c.2989C>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001378991.1:c.2959C>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001378992.1:c.2941C>G - missense variant - [Sequence Ontology: SO:0001583]
NM_004082.5:c.3010C>G - missense variant - [Sequence Ontology: SO:0001583]
NM_023019.4:c.2608C>G - missense variant - [Sequence Ontology: SO:0001583]
NR_033935.2:n.3073C>G - non-coding transcript variant - [Sequence Ontology: SO:0001619]

Condition(s)

Name:: Inborn genetic diseases
Identifiers:: MeSH: D030342; MedGen: C0950123

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV002753333	Ambry Genetics	criteria provided, single submitter (Ambry Variant Classification Scheme 2023)	Likely benign (Jan 2, 2024)	germline	clinical testing	Citation Link

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV002753333

Ambry Genetics

criteria provided, single submitter

(Ambry Variant Classification Scheme 2023)

Likely benign
(Jan 2, 2024)

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, SCV002753333.2

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

#	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 13, 2024

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