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NM_004082.5(DCTN1):c.2761C>G (p.Pro921Ala) AND multiple conditions

Germline classification:
Uncertain significance (1 submission)
Last evaluated:
Nov 6, 2022
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:
RCV003795032.2

Allele description [Variation Report for NM_004082.5(DCTN1):c.2761C>G (p.Pro921Ala)]

NM_004082.5(DCTN1):c.2761C>G (p.Pro921Ala)

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.2761C>G (p.Pro921Ala)
HGVS:
  • NC_000002.12:g.74366018G>C
  • NG_008735.2:g.31070C>G
  • NM_001135040.3:c.2701C>G
  • NM_001135041.3:c.2359C>G
  • NM_001190836.2:c.2650C>G
  • NM_001190837.2:c.2740C>G
  • NM_001378991.1:c.2710C>G
  • NM_001378992.1:c.2692C>G
  • NM_004082.5:c.2761C>GMANE SELECT
  • NM_023019.4:c.2359C>G
  • NP_001128512.1:p.Pro901Ala
  • NP_001128513.1:p.Pro787Ala
  • NP_001177765.1:p.Pro884Ala
  • NP_001177765.1:p.Pro884Ala
  • NP_001177766.1:p.Pro914Ala
  • NP_001365920.1:p.Pro904Ala
  • NP_001365921.1:p.Pro898Ala
  • NP_004073.2:p.Pro921Ala
  • NP_004073.2:p.Pro921Ala
  • NP_075408.1:p.Pro787Ala
  • NP_075408.1:p.Pro787Ala
  • LRG_237t1:c.2761C>G
  • LRG_237t2:c.2650C>G
  • LRG_237t3:c.2359C>G
  • LRG_237:g.31070C>G
  • LRG_237p1:p.Pro921Ala
  • LRG_237p2:p.Pro884Ala
  • LRG_237p3:p.Pro787Ala
  • NC_000002.11:g.74593145G>C
  • NM_001190836.1:c.2650C>G
  • NM_004082.4:c.2761C>G
  • NM_023019.3:c.2359C>G
  • NR_033935.2:n.2824C>G
Protein change:
P787A
Molecular consequence:
  • NM_001135040.3:c.2701C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001135041.3:c.2359C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001190836.2:c.2650C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001190837.2:c.2740C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001378991.1:c.2710C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001378992.1:c.2692C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_004082.5:c.2761C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_023019.4:c.2359C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NR_033935.2:n.2824C>G - non-coding transcript variant - [Sequence Ontology: SO:0001619]

Condition(s)

Name:
Amyotrophic lateral sclerosis type 1 (ALS1)
Synonyms:
AMYOTROPHIC LATERAL SCLEROSIS 1, FAMILIAL
Identifiers:
MONDO: MONDO:0007103; MedGen: C1862939; Orphanet: 803; OMIM: 105400
Name:
Perry syndrome
Synonyms:
Parkinsonism with alveolar hypoventilation and mental depression
Identifiers:
MONDO: MONDO:0008201; MedGen: C1868594; Orphanet: 178509; OMIM: 168605
Name:
Neuronopathy, distal hereditary motor, type 7B
Synonyms:
HMN VIIB; LOWER MOTOR NEURON DISEASE, DYNACTIN TYPE; NEURONOPATHY, DISTAL HEREDITARY MOTOR, AUTOSOMAL DOMINANT 14; See all synonyms [MedGen]
Identifiers:
MONDO: MONDO:0011879; MedGen: C1843315; Orphanet: 139589; OMIM: 607641

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Assertion and evidence details

Submission AccessionSubmitterReview Status
(Assertion method)
Clinical Significance
(Last evaluated)
OriginMethodCitations
SCV004588756Labcorp Genetics (formerly Invitae), Labcorp
criteria provided, single submitter

(Invitae Variant Classification Sherloc (09022015))
Uncertain significance
(Nov 6, 2022)
germlineclinical testing

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

Summary from all submissions

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

Citations

PubMed

Sherloc: a comprehensive refinement of the ACMG-AMP variant classification criteria.

Nykamp K, Anderson M, Powers M, Garcia J, Herrera B, Ho YY, Kobayashi Y, Patil N, Thusberg J, Westbrook M; Invitae Clinical Genomics Group., Topper S.

Genet Med. 2017 Oct;19(10):1105-1117. doi: 10.1038/gim.2017.37. Epub 2017 May 11. Erratum in: Genet Med. 2020 Jan;22(1):240. doi: 10.1038/s41436-019-0624-9.

PubMed [citation]
PMID:
28492532
PMCID:
PMC5632818

Details of each submission

From Labcorp Genetics (formerly Invitae), Labcorp, SCV004588756.1

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not providednot providednot providednot providedclinical testing PubMed (1)

Description

This variant has not been reported in the literature in individuals affected with DCTN1-related conditions. This variant is not present in population databases (gnomAD no frequency). This sequence change replaces proline, which is neutral and non-polar, with alanine, which is neutral and non-polar, at codon 921 of the DCTN1 protein (p.Pro921Ala). Algorithms developed to predict the effect of missense changes on protein structure and function are either unavailable or do not agree on the potential impact of this missense change (SIFT: "Deleterious"; PolyPhen-2: "Benign"; Align-GVGD: "Class C25"). In summary, the available evidence is currently insufficient to determine the role of this variant in disease. Therefore, it has been classified as a Variant of Uncertain Significance. Algorithms developed to predict the effect of sequence changes on RNA splicing suggest that this variant may disrupt the consensus splice site.

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

Last Updated: Sep 29, 2024