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NM_001110556.2(FLNA):c.2401_2402insCT (p.Gln801fs) AND Heterotopia, periventricular, X-linked dominant

Germline classification:
Likely pathogenic (1 submission)
Last evaluated:
Jun 8, 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:
RCV002267691.1

Allele description [Variation Report for NM_001110556.2(FLNA):c.2401_2402insCT (p.Gln801fs)]

NM_001110556.2(FLNA):c.2401_2402insCT (p.Gln801fs)

Gene:
FLNA:filamin A [Gene - OMIM - HGNC]
Variant type:
Insertion
Cytogenetic location:
Xq28
Genomic location:
Preferred name:
NM_001110556.2(FLNA):c.2401_2402insCT (p.Gln801fs)
HGVS:
  • NC_000023.11:g.154362663_154362664insAG
  • NG_011506.2:g.16975_16976insCT
  • NM_001110556.2:c.2401_2402insCTMANE SELECT
  • NM_001456.4:c.2401_2402insCT
  • NP_001104026.1:p.Gln801fs
  • NP_001447.2:p.Gln801fs
  • LRG_1340t1:c.2401_2402insCT
  • LRG_1340:g.16975_16976insCT
  • LRG_1340p1:p.Gln801fs
  • NC_000023.10:g.153591031_153591032insAG
Protein change:
Q801fs
Links:
dbSNP: rs2148114607
NCBI 1000 Genomes Browser:
rs2148114607
Molecular consequence:
  • NM_001110556.2:c.2401_2402insCT - frameshift variant - [Sequence Ontology: SO:0001589]
  • NM_001456.4:c.2401_2402insCT - frameshift variant - [Sequence Ontology: SO:0001589]

Condition(s)

Name:
Heterotopia, periventricular, X-linked dominant (PVNH1)
Synonyms:
PERIVENTRICULAR NODULAR HETEROTOPIA 1; X-linked periventricular heterotopia; Heterotopia familial nodular; See all synonyms [MedGen]
Identifiers:
MONDO: MONDO:0010233; MedGen: C1848213; Orphanet: 2149; Orphanet: 82004; OMIM: 300049

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Assertion and evidence details

Help
Submission AccessionSubmitterReview Status
(Assertion method)		Clinical Significance
(Last evaluated)		OriginMethodCitations
SCV002549864Institute of Human Genetics, University of Leipzig Medical Center
criteria provided, single submitter

(ACMG Guidelines, 2015)		Likely pathogenic
(Jun 8, 2022) 		maternalclinical testing

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

Help

Summary from all submissions

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

Citations

PubMed

Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology.

Richards S, Aziz N, Bale S, Bick D, Das S, Gastier-Foster J, Grody WW, Hegde M, Lyon E, Spector E, Voelkerding K, Rehm HL; ACMG Laboratory Quality Assurance Committee..

Genet Med. 2015 May;17(5):405-24. doi: 10.1038/gim.2015.30. Epub 2015 Mar 5.

PubMed [citation]
PMID:
25741868
PMCID:
PMC4544753

Details of each submission

From Institute of Human Genetics, University of Leipzig Medical Center, SCV002549864.1

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

Description

_x000D_ Criteria applied: PVS1, PM2_SUP

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

Last Updated: May 26, 2024