NM_001267550.2(TTN):c.101708G>A (p.Arg33903His) AND not provided

Clinical significance:Conflicting interpretations of pathogenicity, Likely benign(1);Uncertain significance(1) (Last evaluated: May 20, 2020)

Review status:1 star out of maximum of 4 stars

criteria provided, conflicting interpretations

Based on:
2 submissions [Details]
Record status:
current
Accession:
RCV000172164.4

Allele description [Variation Report for NM_001267550.2(TTN):c.101708G>A (p.Arg33903His)]

NM_001267550.2(TTN):c.101708G>A (p.Arg33903His)

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.101708G>A (p.Arg33903His)
HGVS:
  • NC_000002.12:g.178534907C>T
  • NG_011618.3:g.300896G>A
  • NG_051363.1:g.17081C>T
  • NM_001256850.1:c.96785G>A
  • NM_001267550.2:c.101708G>AMANE SELECT
  • NM_003319.4:c.74513G>A
  • NM_133378.4:c.94004G>A
  • NM_133432.3:c.74888G>A
  • NM_133437.4:c.75089G>A
  • NP_001243779.1:p.Arg32262His
  • NP_001254479.2:p.Arg33903His
  • NP_003310.4:p.Arg24838His
  • NP_596869.4:p.Arg31335His
  • NP_597676.3:p.Arg24963His
  • NP_597681.4:p.Arg25030His
  • LRG_391:g.300896G>A
  • NC_000002.11:g.179399634C>T
Protein change:
R24838H
Links:
dbSNP: rs72629782
NCBI 1000 Genomes Browser:
rs72629782
Molecular consequence:
  • NM_001256850.1:c.96785G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001267550.2:c.101708G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_003319.4:c.74513G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_133378.4:c.94004G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_133432.3:c.74888G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_133437.4:c.75089G>A - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Identifiers:
MedGen: CN517202

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Assertion and evidence details

Submission AccessionSubmitterReview Status
(Assertion method)
Clinical Significance
(Last evaluated)
OriginMethodCitations
SCV000051094Biesecker Lab/Clinical Genomics Section,National Institutes of Health - ClinSeqcriteria provided, single submitter
Uncertain significance
(Jun 24, 2013)
unknownresearch

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

SCV000713891GeneDxcriteria provided, single submitter
Likely benign
(May 20, 2020)
germlineclinical testing

Citation Link

Description

The study set was not selected for affection status in relation to any cancer. Pathogenicity categories were based on literature curation. See Pubmed ID:23861362 for details.

SCV000051094

Medical sequencing

SCV000051094

Summary from all submissions

EthnicityOriginAffectedIndividualsFamiliesChromosomes testedNumber TestedFamily historyMethod
not providedgermlineyesnot providednot providednot providednot providednot providedclinical testing
not providedunknownunknown1not providednot providednot providednot providedresearch

Citations

PubMed

Interpreting secondary cardiac disease variants in an exome cohort.

Ng D, Johnston JJ, Teer JK, Singh LN, Peller LC, Wynter JS, Lewis KL, Cooper DN, Stenson PD, Mullikin JC, Biesecker LG; NIH Intramural Sequencing Center (NISC) Comparative Sequencing Program..

Circ Cardiovasc Genet. 2013 Aug;6(4):337-46. doi: 10.1161/CIRCGENETICS.113.000039. Epub 2013 Jul 16.

PubMed [citation]
PMID:
23861362
PMCID:
PMC3887521

Details of each submission

From Biesecker Lab/Clinical Genomics Section,National Institutes of Health - ClinSeq, SCV000051094.1

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not provided1not providednot providedresearch PubMed (1)
#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1unknownunknownnot providednot providednot provided1not providednot providednot provided

From GeneDx, SCV000713891.1

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not providednot providednot providednot providedclinical testingnot provided
#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1germlineyesnot providednot providednot providednot providednot providednot providednot provided

Last Updated: Oct 8, 2021

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