NM_022489.4(INF2):c.2509C>T (p.Arg837Cys) AND INF2-related disorder

Germline classification:: Likely benign (1 submission)
Last evaluated:: Dec 20, 2022
Review status:: (0/4) 0 stars out of maximum of 4 stars
no assertion criteria provided

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:: RCV003937959.2

Allele description [Variation Report for NM_022489.4(INF2):c.2509C>T (p.Arg837Cys)]

NM_022489.4(INF2):c.2509C>T (p.Arg837Cys)

Gene:

INF2:inverted formin 2 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

14q32.33

Genomic location:

Preferred name:

NM_022489.4(INF2):c.2509C>T (p.Arg837Cys)

HGVS:

NC_000014.9:g.104712452C>T
NG_027684.1:g.27847C>T
NM_001031714.4:c.2509C>T
NM_022489.4:c.2509C>TMANE SELECT
NP_001026884.3:p.Arg837Cys
NP_071934.3:p.Arg837Cys
NC_000014.8:g.105178789C>T
NM_022489.3:c.2509C>T

Protein change:

R837C

Links:

dbSNP: rs201534539

NCBI 1000 Genomes Browser:

rs201534539

Molecular consequence:

NM_001031714.4:c.2509C>T - missense variant - [Sequence Ontology: SO:0001583]
NM_022489.4:c.2509C>T - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Name:: INF2-related disorder
Synonyms:: INF2-related condition
Identifiers:

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV004748167	PreventionGenetics, part of Exact Sciences	no assertion criteria provided	Likely benign (Dec 20, 2022)	germline	clinical testing

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV004748167

PreventionGenetics, part of Exact Sciences

no assertion criteria provided

Likely benign
(Dec 20, 2022)

germline

clinical testing

Help

Summary from all submissions

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

Details of each submission

From PreventionGenetics, part of Exact Sciences, SCV004748167.2

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

Description

This variant is classified as likely benign based on ACMG/AMP sequence variant interpretation guidelines (Richards et al. 2015 PMID: 25741868, with internal and published modifications).

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

Last Updated: Jan 13, 2025

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