NM_002016.2(FLG):c.5871_5872inv (p.Gly1958Arg) AND not provided

Germline classification:: Uncertain significance (1 submission)
Last evaluated:: Jun 6, 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:: RCV002466988.1

Allele description [Variation Report for NM_002016.2(FLG):c.5871_5872inv (p.Gly1958Arg)]

NM_002016.2(FLG):c.5871_5872inv (p.Gly1958Arg)

Genes:

FLG-AS1:FLG antisense RNA 1 [Gene - HGNC]
FLG:filaggrin [Gene - OMIM - HGNC]

Variant type:

Inversion

Cytogenetic location:

1q21.3

Genomic location:

Preferred name:

NM_002016.2(FLG):c.5871_5872inv (p.Gly1958Arg)

HGVS:

NC_000001.11:g.152309014_152309015inv
NG_016190.1:g.21189_21190inv
NM_002016.2:c.5871_5872invMANE SELECT
NP_002007.1:p.Gly1958Arg
NP_002007.1:p.Gly1958Arg
LRG_1028t1:c.5871_5872invTG
LRG_1028:g.21189_21190inv
LRG_1028p1:p.Gly1958Arg
NC_000001.10:g.152281490_152281491inv
NM_002016.1:c.5871_5872delinsCA
NM_002016.1:c.5871_5872invTG

Protein change:

G1958R

Molecular consequence:

NM_002016.2:c.5871_5872inv - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Synonyms:: none provided
Identifiers:: MedGen: CN517202

Recent activity

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GSM4803158[Accession] (3)
GEO DataSets
F-box/WD repeat-containing protein 9 isoform X1 [Homo sapiens]
F-box/WD repeat-containing protein 9 isoform X1 [Homo sapiens]
gi|2462568098|ref|XP_054178309.1|

Protein

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV002762008	GeneDx	criteria provided, single submitter (GeneDx Variant Classification Process June 2021)	Uncertain significance (Jun 6, 2022)	germline	clinical testing	Citation Link

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV002762008

GeneDx

criteria provided, single submitter

(GeneDx Variant Classification Process June 2021)

Uncertain significance
(Jun 6, 2022)

germline

clinical testing

Citation Link

Help

Summary from all submissions

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

Details of each submission

From GeneDx, SCV002762008.1

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

Description

Not observed at significant frequency in large population cohorts (gnomAD); In silico analysis supports that this variant does not alter protein structure/function; Has not been previously published as pathogenic or benign to our knowledge

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

Last Updated: Oct 14, 2023

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