NM_001110556.2(FLNA):c.2565+1G>C AND Heterotopia, periventricular, X-linked dominant

Germline classification:: Pathogenic (1 submission)
Last evaluated:: Oct 9, 2009
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:: RCV000170407.1

Allele description [Variation Report for NM_001110556.2(FLNA):c.2565+1G>C]

NM_001110556.2(FLNA):c.2565+1G>C

Gene:

FLNA:filamin A [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

Xq28

Genomic location:

Preferred name:

NM_001110556.2(FLNA):c.2565+1G>C

HGVS:

NC_000023.11:g.154362417C>G
NG_011506.2:g.17222G>C
NM_001110556.2:c.2565+1G>CMANE SELECT
NM_001456.4:c.2565+1G>C
LRG_1340t1:c.2565+1G>C
LRG_1340:g.17222G>C
NC_000023.10:g.153590785C>G
NM_001110556.1:c.2565+1G>C

Links:

dbSNP: rs786205186

NCBI 1000 Genomes Browser:

rs786205186

Molecular consequence:

NM_001110556.2:c.2565+1G>C - splice donor variant - [Sequence Ontology: SO:0001575]
NM_001456.4:c.2565+1G>C - splice donor variant - [Sequence Ontology: SO:0001575]

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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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV000222832	Claritas Genomics	criteria provided, single submitter (ACMG Guidelines, 2007)	Pathogenic (Oct 9, 2009)	germline	clinical testing	PubMed (1) [See all records that cite this PMID]

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV000222832

Claritas Genomics

criteria provided, single submitter

(ACMG Guidelines, 2007)

Pathogenic
(Oct 9, 2009)

germline

clinical testing

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

Help

Summary from all submissions

Ethnicity	Origin	Affected	Individuals	Families	Chromosomes tested	Number Tested	Family history	Method
not provided	germline	not provided	not provided	not provided	not provided	not provided	not provided	clinical testing

Citations

PubMed

ACMG recommendations for standards for interpretation and reporting of sequence variations: Revisions 2007.

Richards CS, Bale S, Bellissimo DB, Das S, Grody WW, Hegde MR, Lyon E, Ward BE; Molecular Subcommittee of the ACMG Laboratory Quality Assurance Committee..

Genet Med. 2008 Apr;10(4):294-300. doi: 10.1097/GIM.0b013e31816b5cae.

PubMed [citation]

PMID:: 18414213

Details of each submission

From Claritas Genomics, SCV000222832.1

#	Ethnicity	Individuals	Chromosomes Tested	Family History	Method	Citations
1	not provided	not provided	not provided	not provided	clinical testing	PubMed (1)

#	Sample				Method		Observation
#	Origin	Affected	Number tested	Tissue	Purpose	Method	Individuals	Allele frequency	Families	Co-occurrences
1	germline	not provided	not provided	not provided	not provided		not provided	not provided	not provided	not provided

Last Updated: May 26, 2024

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