NM_001267550.2(TTN):c.27485C>T (p.Thr9162Met) AND Left ventricular hypertrophy

Clinical significance:Uncertain significance (Last evaluated: Nov 4, 2015)

Review status:(0/4) 0 stars out of maximum of 4 stars

no assertion criteria provided

Based on:
1 submission [Details]
Record status:
current
Accession:
RCV000678758.1

Allele description [Variation Report for NM_001267550.2(TTN):c.27485C>T (p.Thr9162Met)]

NM_001267550.2(TTN):c.27485C>T (p.Thr9162Met)

Gene:
TTN:titin [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
2q31.2
Genomic location:
Preferred name:
NM_001267550.2(TTN):c.27485C>T (p.Thr9162Met)
HGVS:
  • NC_000002.12:g.178712437G>A
  • NG_011618.3:g.123366C>T
  • NM_001256850.1:c.26534C>T
  • NM_001267550.2:c.27485C>TMANE SELECT
  • NM_003319.4:c.13282+25645C>T
  • NM_133378.4:c.23753C>T
  • NM_133432.3:c.13657+25645C>T
  • NM_133437.4:c.13858+25645C>T
  • NP_001243779.1:p.Thr8845Met
  • NP_001254479.2:p.Thr9162Met
  • NP_596869.4:p.Thr7918Met
  • LRG_391:g.123366C>T
  • NC_000002.11:g.179577164G>A
  • NM_001267550.1:c.27485C>T
Protein change:
T7918M
Links:
dbSNP: rs199793620
NCBI 1000 Genomes Browser:
rs199793620
Molecular consequence:
  • NM_003319.4:c.13282+25645C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_133432.3:c.13657+25645C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_133437.4:c.13858+25645C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001256850.1:c.26534C>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001267550.2:c.27485C>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_133378.4:c.23753C>T - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Name:
Left ventricular hypertrophy
Identifiers:
MedGen: C0149721; Human Phenotype Ontology: HP:0001712

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Assertion and evidence details

Submission AccessionSubmitterReview Status
(Assertion method)
Clinical Significance
(Last evaluated)
OriginMethodCitations
SCV000804937Clinical Molecular Genetics Laboratory,Johns Hopkins All Children's Hospitalno assertion criteria providedUncertain significance
(Nov 4, 2015)
germlineclinical testing

Summary from all submissions

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

Details of each submission

From Clinical Molecular Genetics Laboratory,Johns Hopkins All Children's Hospital, SCV000804937.1

#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: Nov 27, 2021

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