NM_001110556.2(FLNA):c.3256G>A (p.Ala1086Thr) AND FG syndrome 2

Germline classification:: Uncertain significance (1 submission)
Last evaluated:: Nov 3, 2017
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:: RCV001007866.1

Allele description [Variation Report for NM_001110556.2(FLNA):c.3256G>A (p.Ala1086Thr)]

NM_001110556.2(FLNA):c.3256G>A (p.Ala1086Thr)

Gene:

FLNA:filamin A [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

Xq28

Genomic location:

Preferred name:

NM_001110556.2(FLNA):c.3256G>A (p.Ala1086Thr)

HGVS:

NC_000023.11:g.154360539C>T
NG_011506.2:g.19100G>A
NM_001110556.2:c.3256G>AMANE SELECT
NM_001456.4:c.3256G>A
NP_001104026.1:p.Ala1086Thr
NP_001447.2:p.Ala1086Thr
NP_001447.2:p.Ala1086Thr
LRG_1340t1:c.3256G>A
LRG_1340:g.19100G>A
LRG_1340p1:p.Ala1086Thr
NC_000023.10:g.153588907C>T
NC_000023.10:g.153588907C>T
NM_001456.3:c.3256G>A

Protein change:

A1086T

Links:

dbSNP: rs782632029

NCBI 1000 Genomes Browser:

rs782632029

Molecular consequence:

NM_001110556.2:c.3256G>A - missense variant - [Sequence Ontology: SO:0001583]
NM_001456.4:c.3256G>A - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Name:: FG syndrome 2 (FGS2)
Identifiers:: MONDO: MONDO:0010297; MedGen: C1845902; OMIM: 300321

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV001167566	Genomic Medicine Lab, University of California San Francisco - CSER	criteria provided, single submitter (ACMG Guidelines, 2015)	Uncertain significance (Nov 3, 2017)	maternal	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

SCV001167566

Genomic Medicine Lab, University of California San Francisco - CSER

criteria provided, single submitter

(ACMG Guidelines, 2015)

Uncertain significance
(Nov 3, 2017)

maternal

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	maternal	unknown	not provided	not provided	not provided	not provided	not provided	clinical 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 Genomic Medicine Lab, University of California San Francisco - CSER, SCV001167566.1

#	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	maternal	unknown	not provided	not provided	not provided		not provided	not provided	not provided	not provided

Last Updated: Sep 29, 2024

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