NM_001267550.2(TTN):c.27654T>G (p.Val9218=) AND Myopathy, myofibrillar, 9, with early respiratory failure

Clinical significance:Benign (Last evaluated: Jan 12, 2018)

Review status:1 star out of maximum of 4 stars

criteria provided, single submitter

Based on:
1 submission [Details]
Record status:
current
Accession:
RCV000339169.2

Allele description [Variation Report for NM_001267550.2(TTN):c.27654T>G (p.Val9218=)]

NM_001267550.2(TTN):c.27654T>G (p.Val9218=)

Gene:
TTN:titin [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
2q31.2
Genomic location:
Preferred name:
NM_001267550.2(TTN):c.27654T>G (p.Val9218=)
HGVS:
  • NC_000002.12:g.178712176A>C
  • NG_011618.3:g.123627T>G
  • NM_001256850.1:c.26703T>G
  • NM_001267550.2:c.27654T>GMANE SELECT
  • NM_003319.4:c.13282+25906T>G
  • NM_133378.4:c.23922T>G
  • NM_133432.3:c.13657+25906T>G
  • NM_133437.4:c.13858+25906T>G
  • NP_001243779.1:p.Val8901=
  • NP_001254479.2:p.Val9218=
  • NP_596869.4:p.Val7974=
  • LRG_391:g.123627T>G
  • NC_000002.11:g.179576903A>C
Links:
dbSNP: rs780101457
NCBI 1000 Genomes Browser:
rs780101457
Molecular consequence:
  • NM_003319.4:c.13282+25906T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_133432.3:c.13657+25906T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_133437.4:c.13858+25906T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001256850.1:c.26703T>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001267550.2:c.27654T>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_133378.4:c.23922T>G - synonymous variant - [Sequence Ontology: SO:0001819]

Condition(s)

Name:
Myopathy, myofibrillar, 9, with early respiratory failure (MFM9)
Synonyms:
EDSTROM MYOPATHY; MYOPATHY, PROXIMAL, WITH EARLY RESPIRATORY MUSCLE INVOLVEMENT; Hereditary myopathy with early respiratory failure; See all synonyms [MedGen]
Identifiers:
MONDO: MONDO:0011362; MedGen: C1863599; Orphanet: 178464; Orphanet: 34521; OMIM: 603689

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Assertion and evidence details

Submission AccessionSubmitterReview Status
(Assertion method)
Clinical Significance
(Last evaluated)
OriginMethodCitations
SCV000423923Illumina Clinical Services Laboratory,Illuminacriteria provided, single submitter
Benign
(Jan 12, 2018)
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 Illumina Clinical Services Laboratory,Illumina, SCV000423923.3

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

Description

This variant was observed in the ICSL laboratory as part of a predisposition screen in an ostensibly healthy population. It had not been previously curated by ICSL or reported in the Human Gene Mutation Database (HGMD: prior to June 1st, 2018), and was therefore a candidate for classification through an automated scoring system. Utilizing variant allele frequency, disease prevalence and penetrance estimates, and inheritance mode, an automated score was calculated to assess if this variant is too frequent to cause the disease. Based on the score and internal cut-off values, a variant classified as benign is not then subjected to further curation. The score for this variant resulted in a classification of benign for this disease.

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

Last Updated: Nov 27, 2021

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