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NM_001110556.2(FLNA):c.587G>A (p.Arg196Gln) AND not provided

Germline classification:
Uncertain significance (1 submission)
Last evaluated:
Jul 23, 2021
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:
RCV001560948.2

Allele description [Variation Report for NM_001110556.2(FLNA):c.587G>A (p.Arg196Gln)]

NM_001110556.2(FLNA):c.587G>A (p.Arg196Gln)

Gene:
FLNA:filamin A [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
Xq28
Genomic location:
Preferred name:
NM_001110556.2(FLNA):c.587G>A (p.Arg196Gln)
HGVS:
  • NC_000023.11:g.154367877C>T
  • NG_011506.2:g.11762G>A
  • NM_001110556.1:c.587G>A
  • NM_001110556.2:c.587G>AMANE SELECT
  • NM_001456.4:c.587G>A
  • NP_001104026.1:p.Arg196Gln
  • NP_001447.2:p.Arg196Gln
  • LRG_1340t1:c.587G>A
  • LRG_1340:g.11762G>A
  • LRG_1340p1:p.Arg196Gln
  • NC_000023.10:g.153596245C>T
  • NM_001456.3:c.587G>A
Protein change:
R196Q
Links:
dbSNP: rs1569551872
NCBI 1000 Genomes Browser:
rs1569551872
Molecular consequence:
  • NM_001110556.2:c.587G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001456.4:c.587G>A - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Synonyms:
none provided
Identifiers:
MedGen: C3661900

Assertion and evidence details

Help
Submission AccessionSubmitterReview Status
(Assertion method)		Clinical Significance
(Last evaluated)		OriginMethodCitations
SCV001783456GeneDx
criteria provided, single submitter

(GeneDx Variant Classification Process June 2021)		Uncertain significance
(Jul 23, 2021) 		germlineclinical testing

Citation Link

Help

Summary from all submissions

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

Details of each submission

From GeneDx, SCV001783456.1

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

Description

Not observed at a significant frequency in large population cohorts (Lek et al., 2016); In silico analysis, which includes protein predictors and evolutionary conservation, supports that this variant does not alter protein structure/function; Has not been previously published as pathogenic or benign to our knowledge; Different missense changes at this residue (R196W, R196G) have been reported the Human Gene Mutation Database (Stenson et al., 2014)

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

Last Updated: Oct 26, 2024