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NM_004448.4(ERBB2):c.100C>T (p.Arg34Trp) AND not provided

Germline classification:
Uncertain significance (1 submission)
Last evaluated:
May 23, 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:
RCV003053273.2

Allele description

NM_004448.4(ERBB2):c.100C>T (p.Arg34Trp)

Gene:
ERBB2:erb-b2 receptor tyrosine kinase 2 [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
17q12
Genomic location:
Preferred name:
NM_004448.4(ERBB2):c.100C>T (p.Arg34Trp)
HGVS:
  • NC_000017.11:g.39707016C>T
  • NG_007503.1:g.23877C>T
  • NM_001005862.3:c.10C>T
  • NM_001289936.2:c.55C>T
  • NM_001289937.2:c.100C>T
  • NM_001289938.2:c.10C>T
  • NM_001382782.1:c.10C>T
  • NM_001382783.1:c.10C>T
  • NM_001382784.1:c.100C>T
  • NM_001382785.1:c.100C>T
  • NM_001382786.1:c.100C>T
  • NM_001382787.1:c.100C>T
  • NM_001382788.1:c.100C>T
  • NM_001382789.1:c.100C>T
  • NM_001382790.1:c.100C>T
  • NM_001382791.1:c.100C>T
  • NM_001382792.1:c.100C>T
  • NM_001382793.1:c.100C>T
  • NM_001382794.1:c.100C>T
  • NM_001382795.1:c.100C>T
  • NM_001382796.1:c.100C>T
  • NM_001382797.1:c.100C>T
  • NM_001382798.1:c.100C>T
  • NM_001382799.1:c.100C>T
  • NM_001382800.1:c.100C>T
  • NM_001382801.1:c.100C>T
  • NM_001382802.1:c.100C>T
  • NM_001382803.1:c.100C>T
  • NM_001382804.1:c.74-4912C>T
  • NM_001382805.1:c.100C>T
  • NM_001382806.1:c.100C>T
  • NM_004448.4:c.100C>TMANE SELECT
  • NP_001005862.1:p.Arg4Trp
  • NP_001005862.1:p.Arg4Trp
  • NP_001276865.1:p.Arg19Trp
  • NP_001276865.1:p.Arg19Trp
  • NP_001276866.1:p.Arg34Trp
  • NP_001276867.1:p.Arg4Trp
  • NP_001276867.1:p.Arg4Trp
  • NP_001369711.1:p.Arg4Trp
  • NP_001369712.1:p.Arg4Trp
  • NP_001369713.1:p.Arg34Trp
  • NP_001369714.1:p.Arg34Trp
  • NP_001369715.1:p.Arg34Trp
  • NP_001369716.1:p.Arg34Trp
  • NP_001369717.1:p.Arg34Trp
  • NP_001369718.1:p.Arg34Trp
  • NP_001369719.1:p.Arg34Trp
  • NP_001369720.1:p.Arg34Trp
  • NP_001369721.1:p.Arg34Trp
  • NP_001369722.1:p.Arg34Trp
  • NP_001369723.1:p.Arg34Trp
  • NP_001369724.1:p.Arg34Trp
  • NP_001369725.1:p.Arg34Trp
  • NP_001369726.1:p.Arg34Trp
  • NP_001369727.1:p.Arg34Trp
  • NP_001369728.1:p.Arg34Trp
  • NP_001369729.1:p.Arg34Trp
  • NP_001369730.1:p.Arg34Trp
  • NP_001369731.1:p.Arg34Trp
  • NP_001369732.1:p.Arg34Trp
  • NP_001369734.1:p.Arg34Trp
  • NP_001369735.1:p.Arg34Trp
  • NP_004439.2:p.Arg34Trp
  • NP_004439.2:p.Arg34Trp
  • LRG_724t1:c.10C>T
  • LRG_724t2:c.100C>T
  • LRG_724t3:c.10C>T
  • LRG_724t4:c.55C>T
  • LRG_724:g.23877C>T
  • LRG_724p1:p.Arg4Trp
  • LRG_724p2:p.Arg34Trp
  • LRG_724p3:p.Arg4Trp
  • LRG_724p4:p.Arg19Trp
  • NC_000017.10:g.37863269C>T
  • NM_001005862.2:c.10C>T
  • NM_001289936.1:c.55C>T
  • NM_001289938.1:c.10C>T
  • NM_004448.3:c.100C>T
  • NR_110535.2:n.275C>T
Protein change:
R19W
Molecular consequence:
  • NM_001382804.1:c.74-4912C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001005862.3:c.10C>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001289936.2:c.55C>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001289937.2:c.100C>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001289938.2:c.10C>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001382782.1:c.10C>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001382783.1:c.10C>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001382784.1:c.100C>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001382785.1:c.100C>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001382786.1:c.100C>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001382787.1:c.100C>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001382788.1:c.100C>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001382789.1:c.100C>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001382790.1:c.100C>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001382791.1:c.100C>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001382792.1:c.100C>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001382793.1:c.100C>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001382794.1:c.100C>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001382795.1:c.100C>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001382796.1:c.100C>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001382797.1:c.100C>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001382798.1:c.100C>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001382799.1:c.100C>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001382800.1:c.100C>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001382801.1:c.100C>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001382802.1:c.100C>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001382803.1:c.100C>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001382805.1:c.100C>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001382806.1:c.100C>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_004448.4:c.100C>T - missense variant - [Sequence Ontology: SO:0001583]
  • NR_110535.2:n.275C>T - non-coding transcript variant - [Sequence Ontology: SO:0001619]

Condition(s)

Synonyms:
none provided
Identifiers:
MedGen: C3661900

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Assertion and evidence details

Help
Submission AccessionSubmitterReview Status
(Assertion method)		Clinical Significance
(Last evaluated)		OriginMethodCitations
SCV003450606Invitae
criteria provided, single submitter

(Invitae Variant Classification Sherloc (09022015))		Uncertain significance
(May 23, 2023) 		germlineclinical testing

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

Help

Summary from all submissions

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

Citations

PubMed

Sherloc: a comprehensive refinement of the ACMG-AMP variant classification criteria.

Nykamp K, Anderson M, Powers M, Garcia J, Herrera B, Ho YY, Kobayashi Y, Patil N, Thusberg J, Westbrook M; Invitae Clinical Genomics Group., Topper S.

Genet Med. 2017 Oct;19(10):1105-1117. doi: 10.1038/gim.2017.37. Epub 2017 May 11. Erratum in: Genet Med. 2020 Jan;22(1):240. doi: 10.1038/s41436-019-0624-9.

PubMed [citation]
PMID:
28492532
PMCID:
PMC5632818

Details of each submission

From Invitae, SCV003450606.2

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

Description

This sequence change replaces arginine, which is basic and polar, with tryptophan, which is neutral and slightly polar, at codon 34 of the ERBB2 protein (p.Arg34Trp). This variant is present in population databases (rs149937802, gnomAD 0.02%). This variant has not been reported in the literature in individuals affected with ERBB2-related conditions. ClinVar contains an entry for this variant (Variation ID: 2144187). Advanced modeling of protein sequence and biophysical properties (such as structural, functional, and spatial information, amino acid conservation, physicochemical variation, residue mobility, and thermodynamic stability) performed at Invitae indicates that this missense variant is expected to disrupt ERBB2 protein function. In summary, the available evidence is currently insufficient to determine the role of this variant in disease. Therefore, it has been classified as a Variant of Uncertain Significance.

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

Last Updated: Feb 20, 2024