U.S. flag

An official website of the United States government

NM_002230.4(JUP):c.274G>T (p.Gly92Cys) AND multiple conditions

Germline classification:
Uncertain significance (1 submission)
Last evaluated:
Jan 17, 2022
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:
RCV000645198.6

Allele description [Variation Report for NM_002230.4(JUP):c.274G>T (p.Gly92Cys)]

NM_002230.4(JUP):c.274G>T (p.Gly92Cys)

Gene:
JUP:junction plakoglobin [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
17q21.2
Genomic location:
Preferred name:
NM_002230.4(JUP):c.274G>T (p.Gly92Cys)
HGVS:
  • NC_000017.11:g.41769612C>A
  • NG_009090.2:g.22101G>T
  • NM_001352773.2:c.274G>T
  • NM_001352774.2:c.274G>T
  • NM_001352775.2:c.274G>T
  • NM_001352776.2:c.274G>T
  • NM_001352777.2:c.274G>T
  • NM_002230.4:c.274G>TMANE SELECT
  • NM_021991.4:c.274G>T
  • NP_001339702.1:p.Gly92Cys
  • NP_001339703.1:p.Gly92Cys
  • NP_001339704.1:p.Gly92Cys
  • NP_001339705.1:p.Gly92Cys
  • NP_001339706.1:p.Gly92Cys
  • NP_002221.1:p.Gly92Cys
  • NP_068831.1:p.Gly92Cys
  • LRG_401t2:c.274G>T
  • LRG_401:g.22101G>T
  • NC_000017.10:g.39925864C>A
  • NM_002230.2:c.274G>T
Protein change:
G92C
Links:
dbSNP: rs781875765
NCBI 1000 Genomes Browser:
rs781875765
Molecular consequence:
  • NM_001352773.2:c.274G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001352774.2:c.274G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001352775.2:c.274G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001352776.2:c.274G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001352777.2:c.274G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_002230.4:c.274G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_021991.4:c.274G>T - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Name:
Naxos disease (NXD)
Synonyms:
KERATOSIS PALMOPLANTARIS WITH ARRHYTHMOGENIC CARDIOMYOPATHY; PALMOPLANTAR KERATODERMA WITH ARRHYTHMOGENIC RIGHT VENTRICULAR CARDIOMYOPATHY AND WOOLLY HAIR; WOOLLY HAIR, PALMOPLANTAR KERATODERMA, AND CARDIAC ABNORMALITIES; See all synonyms [MedGen]
Identifiers:
MONDO: MONDO:0011017; MedGen: C1832600; Orphanet: 34217; OMIM: 601214
Name:
Arrhythmogenic right ventricular dysplasia 12
Synonyms:
ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 12; Arrhythmogenic right ventricular cardiomyopathy, type 12
Identifiers:
MONDO: MONDO:0012684; MedGen: C1969081; OMIM: 611528

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
SCV000766940Labcorp Genetics (formerly Invitae), Labcorp
criteria provided, single submitter

(Invitae Variant Classification Sherloc (09022015))		Uncertain significance
(Jan 17, 2022) 		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, SCV000766940.5

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

Description

This sequence change replaces glycine, which is neutral and non-polar, with cysteine, which is neutral and slightly polar, at codon 92 of the JUP protein (p.Gly92Cys). The frequency data for this variant in the population databases is considered unreliable, as metrics indicate poor data quality at this position in the gnomAD database. This variant has not been reported in the literature in individuals affected with JUP-related conditions. ClinVar contains an entry for this variant (Variation ID: 449201). Algorithms developed to predict the effect of missense changes on protein structure and function are either unavailable or do not agree on the potential impact of this missense change (SIFT: "Deleterious"; PolyPhen-2: "Possibly Damaging"; Align-GVGD: "Class C0"). 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