NM_004309.6(ARHGDIA):c.458_*278delinsTCTCCTGTCTCGTTGCTGCTTCTGCCTGTG (p.Ala153fs) AND not provided

Germline classification:
Uncertain significance (1 submission)
Last evaluated:
Nov 2, 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:
RCV003577005.1

Allele description

NM_004309.6(ARHGDIA):c.458_*278delinsTCTCCTGTCTCGTTGCTGCTTCTGCCTGTG (p.Ala153fs)

Gene:
ARHGDIA:Rho GDP dissociation inhibitor alpha [Gene - OMIM - HGNC]
Variant type:
Indel
Cytogenetic location:
17q25.3
Genomic location:
Preferred name:
NM_004309.6(ARHGDIA):c.458_*278delinsTCTCCTGTCTCGTTGCTGCTTCTGCCTGTG (p.Ala153fs)
HGVS:
  • NC_000017.11:g.81868598_81869033delinsCACAGGCAGAAGCAGCAACGAGACAGGAGA
  • NG_034210.1:g.7374_7809delinsTCTCCTGTCTCGTTGCTGCTTCTGCCTGTG
  • NG_138099.1:g.707_830delinsCACAGGCAGAAGCAGCAACGAGACAGGAGA
  • NG_138099.2:g.744_867delinsCACAGGCAGAAGCAGCAACGAGACAGGAGA
  • NG_138100.1:g.77_512delinsCACAGGCAGAAGCAGCAACGAGACAGGAGA
  • NM_001185077.3:c.458_*278delinsTCTCCTGTCTCGTTGCTGCTTCTGCCTGTG
  • NM_001185078.3:c.416-90_*278delinsTCTCCTGTCTCGTTGCTGCTTCTGCCTGTG
  • NM_001301240.2:c.458_503-14delinsTCTCCTGTCTCGTTGCTGCTTCTGCCTGTG
  • NM_001301241.2:c.458_503-14delinsTCTCCTGTCTCGTTGCTGCTTCTGCCTGTG
  • NM_001301242.2:c.435+23_781delinsTCTCCTGTCTCGTTGCTGCTTCTGCCTGTG
  • NM_001301243.2:c.593_*278delinsTCTCCTGTCTCGTTGCTGCTTCTGCCTGTG
  • NM_004309.6:c.458_*278delinsTCTCCTGTCTCGTTGCTGCTTCTGCCTGTGMANE SELECT
  • NP_001172006.1:p.Ala153fs
  • NP_001288172.1:p.Ala198fs
  • NP_004300.1:p.Ala153fs
  • NC_000017.10:g.79826474_79826909delinsCACAGGCAGAAGCAGCAACGAGACAGGAGA
  • NR_125441.2:n.448_883delinsTCTCCTGTCTCGTTGCTGCTTCTGCCTGTG
Protein change:
A153fs
Molecular consequence:
  • NM_001185077.3:c.458_*278delinsTCTCCTGTCTCGTTGCTGCTTCTGCCTGTG - frameshift variant - [Sequence Ontology: SO:0001589]
  • NM_001301243.2:c.593_*278delinsTCTCCTGTCTCGTTGCTGCTTCTGCCTGTG - frameshift variant - [Sequence Ontology: SO:0001589]
  • NM_004309.6:c.458_*278delinsTCTCCTGTCTCGTTGCTGCTTCTGCCTGTG - frameshift variant - [Sequence Ontology: SO:0001589]
  • NR_125441.2:n.448_883delinsTCTCCTGTCTCGTTGCTGCTTCTGCCTGTG - non-coding transcript variant - [Sequence Ontology: SO:0001619]
  • NM_001185078.3:c.416-90_*278delinsTCTCCTGTCTCGTTGCTGCTTCTGCCTGTG - splice acceptor variant - [Sequence Ontology: SO:0001574]
  • NM_001301242.2:c.435+23_781delinsTCTCCTGTCTCGTTGCTGCTTCTGCCTGTG - splice acceptor variant - [Sequence Ontology: SO:0001574]
  • NM_001301240.2:c.458_503-14delinsTCTCCTGTCTCGTTGCTGCTTCTGCCTGTG - splice donor variant - [Sequence Ontology: SO:0001575]
  • NM_001301241.2:c.458_503-14delinsTCTCCTGTCTCGTTGCTGCTTCTGCCTGTG - splice donor variant - [Sequence Ontology: SO:0001575]

Condition(s)

Synonyms:
none provided
Identifiers:
MedGen: C3661900

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Assertion and evidence details

Help
Submission AccessionSubmitterReview Status
(Assertion method)		Clinical Significance
(Last evaluated)		OriginMethodCitations
SCV004338161Invitae
criteria provided, single submitter

(Invitae Variant Classification Sherloc (09022015))		Uncertain significance
(Nov 2, 2023) 		germlineclinical testing

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

Help

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 Invitae, SCV004338161.1

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

Description

This sequence change results in a frameshift in the ARHGDIA gene (p.Ala153Valfs*88). While this is not anticipated to result in nonsense mediated decay, it is expected to disrupt the last 52 amino acid(s) of the ARHGDIA protein and extend the protein by 35 additional amino acid residues. This variant is not present in population databases (gnomAD no frequency). This variant has not been reported in the literature in individuals affected with ARHGDIA-related conditions. Experimental studies and prediction algorithms are not available or were not evaluated, and the functional significance of this variant is currently unknown. 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.

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

Last Updated: Feb 20, 2024