U.S. flag

An official website of the United States government

NM_001110556.2(FLNA):c.720+4C>T AND multiple conditions

Germline classification:
Uncertain significance (1 submission)
Last evaluated:
Jul 30, 2020
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:
RCV001305674.5

Allele description [Variation Report for NM_001110556.2(FLNA):c.720+4C>T]

NM_001110556.2(FLNA):c.720+4C>T

Gene:
FLNA:filamin A [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
Xq28
Genomic location:
Preferred name:
NM_001110556.2(FLNA):c.720+4C>T
HGVS:
  • NC_000023.11:g.154367637G>A
  • NG_011506.2:g.12002C>T
  • NM_001110556.2:c.720+4C>TMANE SELECT
  • NM_001456.4:c.720+4C>T
  • LRG_1340t1:c.720+4C>T
  • LRG_1340:g.12002C>T
  • NC_000023.10:g.153596005G>A
  • NG_011506.1:g.12002C>T
Links:
dbSNP: rs1557179583
NCBI 1000 Genomes Browser:
rs1557179583
Molecular consequence:
  • NM_001110556.2:c.720+4C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001456.4:c.720+4C>T - intron variant - [Sequence Ontology: SO:0001627]

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
Name:
Melnick-Needles syndrome (MNS)
Synonyms:
Melnick-Needles osteodysplasty; Osteodysplasty of Melnick and Needles
Identifiers:
MONDO: MONDO:0010650; MedGen: C0025237; Orphanet: 2484; OMIM: 309350
Name:
Oto-palato-digital syndrome, type II (OPD2)
Synonyms:
OPD II SYNDROME; Oto-palato-digital syndrome type 2; Andre syndrome; See all synonyms [MedGen]
Identifiers:
MONDO: MONDO:0010571; MedGen: C1844696; Orphanet: 669; Orphanet: 90652; OMIM: 304120
Name:
Frontometaphyseal dysplasia (FMD1)
Identifiers:
MONDO: MONDO:0015942; MedGen: C0265293; OMIM: PS305620

Recent activity

Clear Turn Off Turn On
  • Exserohilum rostratum
    Exserohilum rostratum
    Molecular Identification of Eight Novel Fungal Pathogens of Date Palm Root Rot in Egypt
    BioProject

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

See more...

Assertion and evidence details

Help
Submission AccessionSubmitterReview Status
(Assertion method)		Clinical Significance
(Last evaluated)		OriginMethodCitations
SCV001495019Labcorp Genetics (formerly Invitae), Labcorp
criteria provided, single submitter

(Invitae Variant Classification Sherloc (09022015))		Uncertain significance
(Jul 30, 2020) 		germlineclinical testing

PubMed (3)
[See all records that cite these PMIDs]

Help

Summary from all submissions

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

Citations

PubMed

Aberrant 5' splice sites in human disease genes: mutation pattern, nucleotide structure and comparison of computational tools that predict their utilization.

Buratti E, Chivers M, Královicová J, Romano M, Baralle M, Krainer AR, Vorechovsky I.

Nucleic Acids Res. 2007;35(13):4250-63. Epub 2007 Jun 18.

PubMed [citation]
PMID:
17576681
PMCID:
PMC1934990

Statistical features of human exons and their flanking regions.

Zhang MQ.

Hum Mol Genet. 1998 May;7(5):919-32.

PubMed [citation]
PMID:
9536098
See all PubMed Citations (3)

Details of each submission

From Labcorp Genetics (formerly Invitae), Labcorp, SCV001495019.4

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not providednot providednot providednot providedclinical testing PubMed (3)

Description

This variant is not present in population databases (ExAC no frequency). This sequence change falls in intron 4 of the FLNA gene. It does not directly change the encoded amino acid sequence of the FLNA protein, but it affects a nucleotide within the consensus splice site of the intron. This variant has not been reported in the literature in individuals with FLNA-related conditions. Nucleotide substitutions within the consensus splice site are a relatively common cause of aberrant splicing (PMID: 17576681, 9536098). Algorithms developed to predict the effect of sequence changes on RNA splicing suggest that this variant is not likely to affect RNA splicing, but this prediction has not been confirmed by published transcriptional studies. 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: Sep 29, 2024