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NM_144991.3(TSPEAR):c.1697A>G (p.Tyr566Cys) AND not provided

Germline classification:
Likely pathogenic (1 submission)
Last evaluated:
Dec 21, 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:
RCV002529321.3

Allele description [Variation Report for NM_144991.3(TSPEAR):c.1697A>G (p.Tyr566Cys)]

NM_144991.3(TSPEAR):c.1697A>G (p.Tyr566Cys)

Genes:
LOC126653398:CDK7 strongly-dependent group 2 enhancer GRCh37_chr21:45928270-45929469 [Gene]
TSPEAR-AS1:TSPEAR antisense RNA 1 [Gene - HGNC]
TSPEAR:thrombospondin type laminin G domain and EAR repeats [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
21q22.3
Genomic location:
Preferred name:
NM_144991.3(TSPEAR):c.1697A>G (p.Tyr566Cys)
HGVS:
  • NC_000021.9:g.44509256T>C
  • NG_033806.1:g.207323A>G
  • NM_001272037.2:c.1493A>G
  • NM_144991.3:c.1697A>GMANE SELECT
  • NP_001258966.1:p.Tyr498Cys
  • NP_659428.2:p.Tyr566Cys
  • NC_000021.8:g.45929139T>C
  • NM_144991.2:c.1697A>G
  • NR_103707.1:n.1219T>C
Protein change:
Y498C
Links:
dbSNP: rs782088056
NCBI 1000 Genomes Browser:
rs782088056
Molecular consequence:
  • NM_001272037.2:c.1493A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_144991.3:c.1697A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NR_103707.1:n.1219T>C - non-coding transcript variant - [Sequence Ontology: SO:0001619]

Condition(s)

Synonyms:
none provided
Identifiers:
MedGen: C3661900

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Assertion and evidence details

Submission AccessionSubmitterReview Status
(Assertion method)
Clinical Significance
(Last evaluated)
OriginMethodCitations
SCV003502360Labcorp Genetics (formerly Invitae), Labcorp
criteria provided, single submitter

(Invitae Variant Classification Sherloc (09022015))
Likely pathogenic
(Dec 21, 2023)
germlineclinical testing

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

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, SCV003502360.2

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

Description

This sequence change replaces tyrosine, which is neutral and polar, with cysteine, which is neutral and slightly polar, at codon 566 of the TSPEAR protein (p.Tyr566Cys). This variant is present in population databases (rs782088056, gnomAD 0.007%). This missense change has been observed in individual(s) with clinical features of ectodermal dysplasia (Invitae). In at least one individual the data is consistent with being in trans (on the opposite chromosome) from a pathogenic variant. ClinVar contains an entry for this variant (Variation ID: 505194). 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) has been performed at Invitae for this missense variant, however the output from this modeling did not meet the statistical confidence thresholds required to predict the impact of this variant on TSPEAR protein function. In summary, the currently available evidence indicates that the variant is pathogenic, but additional data are needed to prove that conclusively. Therefore, this variant has been classified as Likely Pathogenic.

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

Last Updated: Sep 29, 2024