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NM_001018005.2(TPM1):c.713G>T (p.Arg238Leu) AND Hypertrophic cardiomyopathy

Germline classification:
Uncertain significance (1 submission)
Last evaluated:
Dec 9, 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:
RCV000824326.7

Allele description [Variation Report for NM_001018005.2(TPM1):c.713G>T (p.Arg238Leu)]

NM_001018005.2(TPM1):c.713G>T (p.Arg238Leu)

Gene:
TPM1:tropomyosin 1 [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
15q22.2
Genomic location:
Preferred name:
NM_001018005.2(TPM1):c.713G>T (p.Arg238Leu)
HGVS:
  • NC_000015.10:g.63062586G>T
  • NG_007557.1:g.24948G>T
  • NM_000366.6:c.713G>T
  • NM_001018004.2:c.713G>T
  • NM_001018005.2:c.713G>TMANE SELECT
  • NM_001018006.2:c.713G>T
  • NM_001018007.2:c.713G>T
  • NM_001018008.2:c.605G>T
  • NM_001018020.2:c.713G>T
  • NM_001301244.2:c.713G>T
  • NM_001301289.2:c.605G>T
  • NM_001330344.2:c.605G>T
  • NM_001330346.2:c.605G>T
  • NM_001330351.2:c.605G>T
  • NM_001365776.1:c.713G>T
  • NM_001365777.1:c.713G>T
  • NM_001365778.1:c.839G>T
  • NM_001365779.1:c.713G>T
  • NM_001365780.1:c.605G>T
  • NM_001365781.2:c.605G>T
  • NM_001365782.1:c.605G>T
  • NP_000357.3:p.Arg238Leu
  • NP_001018004.1:p.Arg238Leu
  • NP_001018005.1:p.Arg238Leu
  • NP_001018006.1:p.Arg238Leu
  • NP_001018007.1:p.Arg238Leu
  • NP_001018008.1:p.Arg202Leu
  • NP_001018020.1:p.Arg238Leu
  • NP_001288173.1:p.Arg238Leu
  • NP_001288218.1:p.Arg202Leu
  • NP_001317273.1:p.Arg202Leu
  • NP_001317275.1:p.Arg202Leu
  • NP_001317280.1:p.Arg202Leu
  • NP_001352705.1:p.Arg238Leu
  • NP_001352706.1:p.Arg238Leu
  • NP_001352707.1:p.Arg280Leu
  • NP_001352708.1:p.Arg238Leu
  • NP_001352709.1:p.Arg202Leu
  • NP_001352710.1:p.Arg202Leu
  • NP_001352711.1:p.Arg202Leu
  • LRG_387t1:c.713G>T
  • LRG_387:g.24948G>T
  • LRG_387p1:p.Arg238Leu
  • NC_000015.9:g.63354785G>T
  • NM_001018005.1:c.713G>T
Protein change:
R202L
Links:
dbSNP: rs777716347
NCBI 1000 Genomes Browser:
rs777716347
Molecular consequence:
  • NM_000366.6:c.713G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001018004.2:c.713G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001018005.2:c.713G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001018006.2:c.713G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001018007.2:c.713G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001018008.2:c.605G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001018020.2:c.713G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001301244.2:c.713G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001301289.2:c.605G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001330344.2:c.605G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001330346.2:c.605G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001330351.2:c.605G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001365776.1:c.713G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001365777.1:c.713G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001365778.1:c.839G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001365779.1:c.713G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001365780.1:c.605G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001365781.2:c.605G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001365782.1:c.605G>T - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Name:
Hypertrophic cardiomyopathy
Synonyms:
HYPERTROPHIC MYOCARDIOPATHY
Identifiers:
MONDO: MONDO:0005045; MeSH: D002312; MedGen: C0007194; Human Phenotype Ontology: HP:0001639

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Assertion and evidence details

Help
Submission AccessionSubmitterReview Status
(Assertion method)		Clinical Significance
(Last evaluated)		OriginMethodCitations
SCV000965220Labcorp Genetics (formerly Invitae), Labcorp
criteria provided, single submitter

(Invitae Variant Classification Sherloc (09022015))		Uncertain significance
(Dec 9, 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, SCV000965220.6

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

Description

ClinVar contains an entry for this variant (Variation ID: 665938). This missense change has been observed in individual(s) with clinical features of TPM1-related conditions (Invitae). This variant is not present in population databases (gnomAD no frequency). This sequence change replaces arginine, which is basic and polar, with leucine, which is neutral and non-polar, at codon 238 of the TPM1 protein (p.Arg238Leu). Algorithms developed to predict the effect of missense changes on protein structure and function (SIFT, PolyPhen-2, Align-GVGD) all suggest that this variant is likely to be disruptive. This variant disrupts the p.Arg238 amino acid residue in TPM1. Other variant(s) that disrupt this residue have been observed in individuals with TPM1-related conditions (Invitae), which suggests that this may be a clinically significant amino acid residue. 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