NM_001267550.2(TTN):c.88787C>G (p.Thr29596Ser) AND Cardiovascular phenotype

Germline classification:
Uncertain significance (1 submission)
Last evaluated:
Mar 17, 2020
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:
RCV002354434.2

Allele description [Variation Report for NM_001267550.2(TTN):c.88787C>G (p.Thr29596Ser)]

NM_001267550.2(TTN):c.88787C>G (p.Thr29596Ser)

Genes:
TTN-AS1:TTN antisense RNA 1 [Gene - HGNC]
TTN:titin [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
2q31.2
Genomic location:
Preferred name:
NM_001267550.2(TTN):c.88787C>G (p.Thr29596Ser)
HGVS:
  • NC_000002.12:g.178554560G>C
  • NG_011618.3:g.281243C>G
  • NG_051363.1:g.36734G>C
  • NM_001256850.1:c.83864C>G
  • NM_001267550.2:c.88787C>GMANE SELECT
  • NM_003319.4:c.61592C>G
  • NM_133378.4:c.81083C>G
  • NM_133432.3:c.61967C>G
  • NM_133437.4:c.62168C>G
  • NP_001243779.1:p.Thr27955Ser
  • NP_001254479.2:p.Thr29596Ser
  • NP_003310.4:p.Thr20531Ser
  • NP_596869.4:p.Thr27028Ser
  • NP_597676.3:p.Thr20656Ser
  • NP_597681.4:p.Thr20723Ser
  • LRG_391:g.281243C>G
  • NC_000002.11:g.179419287G>C
  • NM_001267550.1:c.88787C>G
  • NM_001267550.2:c.88787C>G
  • NM_003319.4:c.61592C>G
Protein change:
T20531S
Links:
dbSNP: rs786205371
NCBI 1000 Genomes Browser:
rs786205371
Molecular consequence:
  • NM_001256850.1:c.83864C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001267550.2:c.88787C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_003319.4:c.61592C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_133378.4:c.81083C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_133432.3:c.61967C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_133437.4:c.62168C>G - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Name:
Cardiovascular phenotype
Identifiers:
MedGen: CN230736

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Assertion and evidence details

Help
Submission AccessionSubmitterReview Status
(Assertion method)		Clinical Significance
(Last evaluated)		OriginMethodCitations
SCV002654496Ambry Genetics
criteria provided, single submitter

(Ambry Variant Classification Scheme 2023)		Uncertain significance
(Mar 17, 2020) 		germlineclinical testing

Citation Link

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Summary from all submissions

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

Details of each submission

From Ambry Genetics, SCV002654496.2

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

Description

The p.T20531S variant (also known as c.61592C>G), located in coding exon 159 of the TTN gene, results from a C to G substitution at nucleotide position 61592. The threonine at codon 20531 is replaced by serine, an amino acid with similar properties. This amino acid position is not well conserved in available vertebrate species. In addition, this alteration is predicted to be tolerated by in silico analysis. Since supporting evidence is limited at this time, the clinical significance of this alteration remains unclear.

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

Last Updated: Jul 29, 2024