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NM_001267550.2(TTN):c.58939G>A (p.Gly19647Arg) AND Cardiovascular phenotype

Germline classification:
Uncertain significance (1 submission)
Last evaluated:
Mar 29, 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:
RCV002322178.9

Allele description [Variation Report for NM_001267550.2(TTN):c.58939G>A (p.Gly19647Arg)]

NM_001267550.2(TTN):c.58939G>A (p.Gly19647Arg)

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.58939G>A (p.Gly19647Arg)
HGVS:
  • NC_000002.12:g.178593269C>T
  • NG_011618.3:g.242534G>A
  • NG_051363.1:g.75443C>T
  • NM_001256850.1:c.54016G>A
  • NM_001267550.2:c.58939G>AMANE SELECT
  • NM_003319.4:c.31744G>A
  • NM_133378.4:c.51235G>A
  • NM_133432.3:c.32119G>A
  • NM_133437.4:c.32320G>A
  • NP_001243779.1:p.Gly18006Arg
  • NP_001254479.2:p.Gly19647Arg
  • NP_003310.4:p.Gly10582Arg
  • NP_596869.4:p.Gly17079Arg
  • NP_597676.3:p.Gly10707Arg
  • NP_597681.4:p.Gly10774Arg
  • LRG_391:g.242534G>A
  • NC_000002.11:g.179457996C>T
  • NM_001267550.2:c.58939G>A
Protein change:
G10582R
Links:
dbSNP: rs201430346
NCBI 1000 Genomes Browser:
rs201430346
Molecular consequence:
  • NM_001256850.1:c.54016G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001267550.2:c.58939G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_003319.4:c.31744G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_133378.4:c.51235G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_133432.3:c.32119G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_133437.4:c.32320G>A - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Name:
Cardiovascular phenotype
Identifiers:
MedGen: CN230736

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Assertion and evidence details

Submission AccessionSubmitterReview Status
(Assertion method)
Clinical Significance
(Last evaluated)
OriginMethodCitations
SCV002609731Ambry Genetics
criteria provided, single submitter

(Ambry Variant Classification Scheme 2023)
Uncertain significance
(Mar 29, 2019)
germlineclinical testing

Citation Link

Summary from all submissions

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

Details of each submission

From Ambry Genetics, SCV002609731.2

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

Description

The p.G10582R variant (also known as c.31744G>A), located in coding exon 126 of the TTN gene, results from a G to A substitution at nucleotide position 31744. The glycine at codon 10582 is replaced by arginine, an amino acid with dissimilar properties. This amino acid position is highly conserved in available vertebrate species. In addition, the in silico prediction for this alteration is inconclusive. 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: Nov 24, 2024