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NM_001018005.2(TPM1):c.271C>T (p.Arg91Cys) AND not provided

Germline classification:
Uncertain significance (1 submission)
Last evaluated:
May 14, 2019
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:
RCV001760087.2

Allele description [Variation Report for NM_001018005.2(TPM1):c.271C>T (p.Arg91Cys)]

NM_001018005.2(TPM1):c.271C>T (p.Arg91Cys)

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.271C>T (p.Arg91Cys)
HGVS:
  • NC_000015.10:g.63057015C>T
  • NG_007557.1:g.19377C>T
  • NM_000366.6:c.271C>T
  • NM_001018004.2:c.271C>T
  • NM_001018005.2:c.271C>TMANE SELECT
  • NM_001018006.2:c.271C>T
  • NM_001018007.2:c.271C>T
  • NM_001018008.2:c.163C>T
  • NM_001018020.2:c.271C>T
  • NM_001301244.2:c.271C>T
  • NM_001301289.2:c.163C>T
  • NM_001330344.2:c.163C>T
  • NM_001330346.2:c.163C>T
  • NM_001330351.2:c.163C>T
  • NM_001365776.1:c.271C>T
  • NM_001365777.1:c.271C>T
  • NM_001365778.1:c.397C>T
  • NM_001365779.1:c.271C>T
  • NM_001365780.1:c.163C>T
  • NM_001365781.2:c.163C>T
  • NM_001365782.1:c.163C>T
  • NP_000357.3:p.Arg91Cys
  • NP_001018004.1:p.Arg91Cys
  • NP_001018005.1:p.Arg91Cys
  • NP_001018006.1:p.Arg91Cys
  • NP_001018007.1:p.Arg91Cys
  • NP_001018008.1:p.Arg55Cys
  • NP_001018020.1:p.Arg91Cys
  • NP_001288173.1:p.Arg91Cys
  • NP_001288218.1:p.Arg55Cys
  • NP_001317273.1:p.Arg55Cys
  • NP_001317275.1:p.Arg55Cys
  • NP_001317280.1:p.Arg55Cys
  • NP_001352705.1:p.Arg91Cys
  • NP_001352706.1:p.Arg91Cys
  • NP_001352707.1:p.Arg133Cys
  • NP_001352708.1:p.Arg91Cys
  • NP_001352709.1:p.Arg55Cys
  • NP_001352710.1:p.Arg55Cys
  • NP_001352711.1:p.Arg55Cys
  • LRG_387t1:c.271C>T
  • LRG_387:g.19377C>T
  • LRG_387p1:p.Arg91Cys
  • NC_000015.9:g.63349214C>T
  • NC_000015.9:g.63349214C>T
  • NM_001018005.1:c.271C>T
Protein change:
R133C
Links:
dbSNP: rs1266444831
NCBI 1000 Genomes Browser:
rs1266444831
Molecular consequence:
  • NM_000366.6:c.271C>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001018004.2:c.271C>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001018005.2:c.271C>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001018006.2:c.271C>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001018007.2:c.271C>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001018008.2:c.163C>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001018020.2:c.271C>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001301244.2:c.271C>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001301289.2:c.163C>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001330344.2:c.163C>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001330346.2:c.163C>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001330351.2:c.163C>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001365776.1:c.271C>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001365777.1:c.271C>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001365778.1:c.397C>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001365779.1:c.271C>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001365780.1:c.163C>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001365781.2:c.163C>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001365782.1:c.163C>T - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Synonyms:
none provided
Identifiers:
MedGen: C3661900

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Assertion and evidence details

Help
Submission AccessionSubmitterReview Status
(Assertion method)		Clinical Significance
(Last evaluated)		OriginMethodCitations
SCV001989797GeneDx
criteria provided, single submitter

(GeneDx Variant Classification Process June 2021)		Uncertain significance
(May 14, 2019) 		germlineclinical testing

Citation Link

Help

Summary from all submissions

EthnicityOriginAffectedIndividualsFamiliesChromosomes testedNumber TestedFamily historyMethod
not providedgermlineyesnot providednot providednot providednot providednot providedclinical testing

Details of each submission

From GeneDx, SCV001989797.2

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not providednot providednot providednot providedclinical testingnot provided

Description

Has not been previously published as pathogenic or benign to our knowledge; Not observed at a significant frequency in large population cohorts (Lek et al., 2016); In silico analysis, which includes protein predictors and evolutionary conservation, supports a deleterious effect; Missense variants in nearby residues (I92M, I92T, V95A) have been reported in the Human Gene Mutation Database and at GeneDx in association with cardiomyopathy (Stenson et al., 2014); however additional evidence is needed to definitively determine pathogenicity

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

Last Updated: Sep 29, 2024