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NM_000053.4(ATP7B):c.1153G>C (p.Glu385Gln) AND Wilson disease

Germline classification:
Uncertain significance (1 submission)
Last evaluated:
Dec 15, 2021
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:
RCV001966467.4

Allele description [Variation Report for NM_000053.4(ATP7B):c.1153G>C (p.Glu385Gln)]

NM_000053.4(ATP7B):c.1153G>C (p.Glu385Gln)

Gene:
ATP7B:ATPase copper transporting beta [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
13q14.3
Genomic location:
Preferred name:
NM_000053.4(ATP7B):c.1153G>C (p.Glu385Gln)
HGVS:
  • NC_000013.11:g.51974067C>G
  • NG_008806.1:g.42428G>C
  • NM_000053.4:c.1153G>CMANE SELECT
  • NM_001005918.3:c.1153G>C
  • NM_001243182.2:c.820G>C
  • NM_001330578.2:c.1153G>C
  • NM_001330579.2:c.1153G>C
  • NP_000044.2:p.Glu385Gln
  • NP_001005918.1:p.Glu385Gln
  • NP_001230111.1:p.Glu274Gln
  • NP_001317507.1:p.Glu385Gln
  • NP_001317508.1:p.Glu385Gln
  • NC_000013.10:g.52548203C>G
Protein change:
E274Q
Links:
dbSNP: rs772069735
NCBI 1000 Genomes Browser:
rs772069735
Molecular consequence:
  • NM_000053.4:c.1153G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001005918.3:c.1153G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001243182.2:c.820G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001330578.2:c.1153G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001330579.2:c.1153G>C - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Name:
Wilson disease (WND)
Synonyms:
Wilson's disease; Hepatolenticular degeneration
Identifiers:
MONDO: MONDO:0010200; MedGen: C0019202; Orphanet: 905; OMIM: 277900

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Assertion and evidence details

Help
Submission AccessionSubmitterReview Status
(Assertion method)		Clinical Significance
(Last evaluated)		OriginMethodCitations
SCV002254489Labcorp Genetics (formerly Invitae), Labcorp
criteria provided, single submitter

(Invitae Variant Classification Sherloc (09022015))		Uncertain significance
(Dec 15, 2021) 		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 Labcorp Genetics (formerly Invitae), Labcorp, SCV002254489.3

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

Description

This sequence change replaces glutamic acid, which is acidic and polar, with glutamine, which is neutral and polar, at codon 385 of the ATP7B protein (p.Glu385Gln). This variant is not present in population databases (gnomAD no frequency). This variant has not been reported in the literature in individuals affected with ATP7B-related conditions. 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 not expected to disrupt ATP7B 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: Sep 29, 2024