NM_001267550.2(TTN):c.86949A>G (p.Glu28983=) AND not provided

Clinical significance:Uncertain significance (Last evaluated: Nov 1, 2020)

Review status:2 stars out of maximum of 4 stars

criteria provided, multiple submitters, no conflicts

Based on:
2 submissions [Details]
Record status:
current
Accession:
RCV000725274.5

Allele description [Variation Report for NM_001267550.2(TTN):c.86949A>G (p.Glu28983=)]

NM_001267550.2(TTN):c.86949A>G (p.Glu28983=)

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.86949A>G (p.Glu28983=)
HGVS:
  • NC_000002.12:g.178558510T>C
  • NG_011618.3:g.277293A>G
  • NG_051363.1:g.40684T>C
  • NM_001256850.1:c.82026A>G
  • NM_001267550.2:c.86949A>GMANE SELECT
  • NM_003319.4:c.59754A>G
  • NM_133378.4:c.79245A>G
  • NM_133432.3:c.60129A>G
  • NM_133437.4:c.60330A>G
  • NP_001243779.1:p.Glu27342=
  • NP_001254479.2:p.Glu28983=
  • NP_003310.4:p.Glu19918=
  • NP_596869.4:p.Glu26415=
  • NP_597676.3:p.Glu20043=
  • NP_597681.4:p.Glu20110=
  • LRG_391:g.277293A>G
  • NC_000002.11:g.179423237T>C
Links:
dbSNP: rs375565646
NCBI 1000 Genomes Browser:
rs375565646
Molecular consequence:
  • NM_001256850.1:c.82026A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001267550.2:c.86949A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_003319.4:c.59754A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_133378.4:c.79245A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_133432.3:c.60129A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_133437.4:c.60330A>G - synonymous variant - [Sequence Ontology: SO:0001819]
Observations:
5

Condition(s)

Identifiers:
MedGen: CN517202

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Assertion and evidence details

Submission AccessionSubmitterReview Status
(Assertion method)
Clinical Significance
(Last evaluated)
OriginMethodCitations
SCV000335537EGL Genetic Diagnostics, Eurofins Clinical Diagnosticscriteria provided, single submitter
Uncertain significance
(Oct 22, 2015)
germlineclinical testing

Citation Link,

SCV001152693CeGaT Praxis fuer Humangenetik Tuebingencriteria provided, single submitter
Uncertain significance
(Nov 1, 2020)
germlineclinical testing

Citation Link

Summary from all submissions

EthnicityOriginAffectedIndividualsFamiliesChromosomes testedNumber TestedFamily historyMethod
not providedgermlineunknown2not providednot providednot providednot providedclinical testing
not providedgermlineyes3not providednot providednot providednot providedclinical testing

Details of each submission

From EGL Genetic Diagnostics, Eurofins Clinical Diagnostics, SCV000335537.3

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not provided2not providednot providedclinical testingnot provided
#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1germlineunknownnot providednot providednot provided2not providednot providednot provided

From CeGaT Praxis fuer Humangenetik Tuebingen, SCV001152693.6

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

Last Updated: Sep 6, 2021

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