NM_001267550.2(TTN):c.5740G>A (p.Ala1914Thr) AND not provided

Clinical significance:Conflicting interpretations of pathogenicity, Likely benign(1);Uncertain significance(1) (Last evaluated: Jul 25, 2018)

Review status:1 star out of maximum of 4 stars

criteria provided, conflicting interpretations

Based on:
2 submissions [Details]
Record status:
current
Accession:
RCV000725466.4

Allele description [Variation Report for NM_001267550.2(TTN):c.5740G>A (p.Ala1914Thr)]

NM_001267550.2(TTN):c.5740G>A (p.Ala1914Thr)

Gene:
TTN:titin [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
2q31.2
Genomic location:
Preferred name:
NM_001267550.2(TTN):c.5740G>A (p.Ala1914Thr)
HGVS:
  • NC_000002.12:g.178776124C>T
  • NG_011618.3:g.59679G>A
  • NM_001256850.1:c.5740G>A
  • NM_001267550.2:c.5740G>AMANE SELECT
  • NM_003319.4:c.5602G>A
  • NM_133378.4:c.5740G>A
  • NM_133379.5:c.5740G>A
  • NM_133432.3:c.5602G>A
  • NM_133437.4:c.5602G>A
  • NP_001243779.1:p.Ala1914Thr
  • NP_001254479.2:p.Ala1914Thr
  • NP_003310.4:p.Ala1868Thr
  • NP_596869.4:p.Ala1914Thr
  • NP_596870.2:p.Ala1914Thr
  • NP_597676.3:p.Ala1868Thr
  • NP_597681.4:p.Ala1868Thr
  • LRG_391:g.59679G>A
  • NC_000002.11:g.179640851C>T
Protein change:
A1868T
Links:
dbSNP: rs118161093
NCBI 1000 Genomes Browser:
rs118161093
Molecular consequence:
  • NM_001256850.1:c.5740G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001267550.2:c.5740G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_003319.4:c.5602G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_133378.4:c.5740G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_133379.5:c.5740G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_133432.3:c.5602G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_133437.4:c.5602G>A - missense variant - [Sequence Ontology: SO:0001583]
Observations:
3

Condition(s)

Identifiers:
MedGen: CN517202

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Assertion and evidence details

Submission AccessionSubmitterReview Status
(Assertion method)
Clinical Significance
(Last evaluated)
OriginMethodCitations
SCV000700983EGL Genetic Diagnostics, Eurofins Clinical Diagnosticscriteria provided, single submitter
Uncertain significance
(Jun 29, 2017)
germlineclinical testing

Citation Link,

SCV000730323GeneDxcriteria provided, single submitter
Likely benign
(Jul 25, 2018)
germlineclinical testing

Citation Link

Summary from all submissions

EthnicityOriginAffectedIndividualsFamiliesChromosomes testedNumber TestedFamily historyMethod
not providedgermlineunknown3not providednot providednot providednot providedclinical testing
not providedgermlineyesnot providednot providednot providednot providednot providedclinical testing

Details of each submission

From EGL Genetic Diagnostics, Eurofins Clinical Diagnostics, SCV000700983.2

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not provided3not providednot providedclinical testingnot provided
#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1germlineunknownnot providednot providednot provided3not providednot providednot provided

From GeneDx, SCV000730323.1

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

Description

This variant is associated with the following publications: (PMID: 27066551, 28771489)

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

Last Updated: Nov 27, 2021

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