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NM_000268.4(NF2):c.1232G>A (p.Arg411His) AND Hereditary cancer-predisposing syndrome

Germline classification:
Likely benign (1 submission)
Last evaluated:
May 19, 2023
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:
RCV001010465.4

Allele description [Variation Report for NM_000268.4(NF2):c.1232G>A (p.Arg411His)]

NM_000268.4(NF2):c.1232G>A (p.Arg411His)

Gene:
NF2:NF2, moesin-ezrin-radixin like (MERLIN) tumor suppressor [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
22q12.2
Genomic location:
Preferred name:
NM_000268.4(NF2):c.1232G>A (p.Arg411His)
HGVS:
  • NC_000022.11:g.29673378G>A
  • NG_009057.1:g.74823G>A
  • NM_000268.4:c.1232G>AMANE SELECT
  • NM_016418.5:c.1232G>A
  • NM_181825.3:c.1232G>A
  • NM_181828.3:c.1106G>A
  • NM_181829.3:c.1109G>A
  • NM_181830.3:c.983G>A
  • NM_181831.3:c.983G>A
  • NM_181832.3:c.1232G>A
  • NM_181833.3:c.448-21374G>A
  • NP_000259.1:p.Arg411His
  • NP_000259.1:p.Arg411His
  • NP_057502.2:p.Arg411His
  • NP_861546.1:p.Arg411His
  • NP_861966.1:p.Arg369His
  • NP_861967.1:p.Arg370His
  • NP_861968.1:p.Arg328His
  • NP_861969.1:p.Arg328His
  • NP_861970.1:p.Arg411His
  • LRG_511t1:c.1232G>A
  • LRG_511t2:c.1232G>A
  • LRG_511:g.74823G>A
  • LRG_511p1:p.Arg411His
  • LRG_511p2:p.Arg411His
  • NC_000022.10:g.30069367G>A
  • NM_000268.3(NF2):c.1232G>A
  • NM_000268.3:c.1232G>A
  • NR_156186.2:n.1714G>A
  • p.Arg411His
Protein change:
R328H
Links:
dbSNP: rs201214090
NCBI 1000 Genomes Browser:
rs201214090
Molecular consequence:
  • NM_181833.3:c.448-21374G>A - intron variant - [Sequence Ontology: SO:0001627]
  • NM_000268.4:c.1232G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_016418.5:c.1232G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_181825.3:c.1232G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_181828.3:c.1106G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_181829.3:c.1109G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_181830.3:c.983G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_181831.3:c.983G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_181832.3:c.1232G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NR_156186.2:n.1714G>A - non-coding transcript variant - [Sequence Ontology: SO:0001619]

Condition(s)

Name:
Hereditary cancer-predisposing syndrome
Synonyms:
Neoplastic Syndromes, Hereditary; Tumor predisposition; Cancer predisposition; See all synonyms [MedGen]
Identifiers:
MONDO: MONDO:0015356; MeSH: D009386; MedGen: C0027672

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Assertion and evidence details

Help
Submission AccessionSubmitterReview Status
(Assertion method)		Clinical Significance
(Last evaluated)		OriginMethodCitations
SCV001170667Ambry Genetics
criteria provided, single submitter

(Ambry Variant Classification Scheme 2023)		Likely benign
(May 19, 2023) 		germlineclinical testing

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

Citation Link

Help

Summary from all submissions

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

Citations

PubMed

Pathogenic Mutations in Cancer-Predisposing Genes: A Survey of 300 Patients with Whole-Genome Sequencing and Lifetime Electronic Health Records.

He KY, Zhao Y, McPherson EW, Li Q, Xia F, Weng C, Wang K, He MM.

PLoS One. 2016;11(12):e0167847. doi: 10.1371/journal.pone.0167847.

PubMed [citation]
PMID:
27930734
PMCID:
PMC5145192

Details of each submission

From Ambry Genetics, SCV001170667.5

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

Description

This alteration is classified as likely benign based on a combination of the following: seen in unaffected individuals, population frequency, intact protein function, lack of segregation with disease, co-occurrence, RNA analysis, in silico models, amino acid conservation, lack of disease association in case-control studies, and/or the mechanism of disease or impacted region is inconsistent with a known cause of pathogenicity.

#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1germlineunknownnot providednot providednot providednot providednot providednot providednot provided

Last Updated: Oct 8, 2024