U.S. flag

An official website of the United States government

NM_024675.4(PALB2):c.3082G>T (p.Gly1028Cys) AND Familial cancer of breast

Germline classification:
Uncertain significance (1 submission)
Last evaluated:
Apr 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:
RCV002299260.4

Allele description [Variation Report for NM_024675.4(PALB2):c.3082G>T (p.Gly1028Cys)]

NM_024675.4(PALB2):c.3082G>T (p.Gly1028Cys)

Gene:
PALB2:partner and localizer of BRCA2 [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
16p12.2
Genomic location:
Preferred name:
NM_024675.4(PALB2):c.3082G>T (p.Gly1028Cys)
HGVS:
  • NC_000016.10:g.23621393C>A
  • NG_007406.1:g.24965G>T
  • NM_001407296.1:c.3022G>T
  • NM_001407297.1:c.3010G>T
  • NM_001407298.1:c.2920G>T
  • NM_001407299.1:c.3082G>T
  • NM_001407301.1:c.3082G>T
  • NM_001407302.1:c.2920G>T
  • NM_001407304.1:c.2197G>T
  • NM_001407305.1:c.2197G>T
  • NM_001407306.1:c.2197G>T
  • NM_001407307.1:c.2035G>T
  • NM_001407308.1:c.2197G>T
  • NM_001407309.1:c.2197G>T
  • NM_001407310.1:c.2197G>T
  • NM_001407311.1:c.2197G>T
  • NM_001407312.1:c.1294G>T
  • NM_001407313.1:c.1294G>T
  • NM_001407314.1:c.616G>T
  • NM_024675.4:c.3082G>TMANE SELECT
  • NP_001394225.1:p.Gly1008Cys
  • NP_001394226.1:p.Gly1004Cys
  • NP_001394227.1:p.Gly974Cys
  • NP_001394228.1:p.Gly1028Cys
  • NP_001394230.1:p.Gly1028Cys
  • NP_001394231.1:p.Gly974Cys
  • NP_001394233.1:p.Gly733Cys
  • NP_001394234.1:p.Gly733Cys
  • NP_001394235.1:p.Gly733Cys
  • NP_001394236.1:p.Gly679Cys
  • NP_001394237.1:p.Gly733Cys
  • NP_001394238.1:p.Gly733Cys
  • NP_001394239.1:p.Gly733Cys
  • NP_001394240.1:p.Gly733Cys
  • NP_001394241.1:p.Gly432Cys
  • NP_001394242.1:p.Gly432Cys
  • NP_001394243.1:p.Gly206Cys
  • NP_078951.2:p.Gly1028Cys
  • NP_078951.2:p.Gly1028Cys
  • LRG_308t1:c.3082G>T
  • LRG_308:g.24965G>T
  • LRG_308p1:p.Gly1028Cys
  • NC_000016.9:g.23632714C>A
  • NM_024675.3:c.3082G>T
Protein change:
G1004C
Molecular consequence:
  • NM_001407296.1:c.3022G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407297.1:c.3010G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407298.1:c.2920G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407299.1:c.3082G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407301.1:c.3082G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407302.1:c.2920G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407304.1:c.2197G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407305.1:c.2197G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407306.1:c.2197G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407307.1:c.2035G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407308.1:c.2197G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407309.1:c.2197G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407310.1:c.2197G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407311.1:c.2197G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407312.1:c.1294G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407313.1:c.1294G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407314.1:c.616G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_024675.4:c.3082G>T - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Name:
Familial cancer of breast
Synonyms:
Breast cancer, familial; Hereditary breast cancer
Identifiers:
MONDO: MONDO:0016419; MedGen: C0346153; OMIM: 114480

Recent activity

Clear Turn Off Turn On

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

See more...

Assertion and evidence details

Help
Submission AccessionSubmitterReview Status
(Assertion method)		Clinical Significance
(Last evaluated)		OriginMethodCitations
SCV002593760Labcorp Genetics (formerly Invitae), Labcorp
criteria provided, single submitter

(Invitae Variant Classification Sherloc (09022015))		Uncertain significance
(Apr 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 Labcorp Genetics (formerly Invitae), Labcorp, SCV002593760.3

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

Description

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. 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 PALB2 protein function. ClinVar contains an entry for this variant (Variation ID: 1714932). This variant has not been reported in the literature in individuals affected with PALB2-related conditions. This variant is not present in population databases (gnomAD no frequency). This sequence change replaces glycine, which is neutral and non-polar, with cysteine, which is neutral and slightly polar, at codon 1028 of the PALB2 protein (p.Gly1028Cys).

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

Last Updated: Sep 29, 2024