NM_001267550.2(TTN):c.97612C>T (p.Arg32538Cys) AND not specified

Clinical significance:Likely benign (Last evaluated: Jan 18, 2019)

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:
RCV000184180.3

Allele description [Variation Report for NM_001267550.2(TTN):c.97612C>T (p.Arg32538Cys)]

NM_001267550.2(TTN):c.97612C>T (p.Arg32538Cys)

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.97612C>T (p.Arg32538Cys)
Other names:
p.R29970C:CGC>TGC
HGVS:
  • NC_000002.12:g.178541465G>A
  • NG_011618.3:g.294338C>T
  • NG_051363.1:g.23639G>A
  • NM_001256850.1:c.92689C>T
  • NM_001267550.2:c.97612C>TMANE SELECT
  • NM_003319.4:c.70417C>T
  • NM_133378.4:c.89908C>T
  • NM_133432.3:c.70792C>T
  • NM_133437.4:c.70993C>T
  • NP_001243779.1:p.Arg30897Cys
  • NP_001254479.2:p.Arg32538Cys
  • NP_003310.4:p.Arg23473Cys
  • NP_596869.4:p.Arg29970Cys
  • NP_597676.3:p.Arg23598Cys
  • NP_597681.4:p.Arg23665Cys
  • LRG_391:g.294338C>T
  • NC_000002.11:g.179406192G>A
  • NM_133379.3:c.*204120C>T
Protein change:
R23473C
Links:
dbSNP: rs761050391
NCBI 1000 Genomes Browser:
rs761050391
Molecular consequence:
  • NM_001256850.1:c.92689C>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001267550.2:c.97612C>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_003319.4:c.70417C>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_133378.4:c.89908C>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_133432.3:c.70792C>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_133437.4:c.70993C>T - missense variant - [Sequence Ontology: SO:0001583]
Observations:
1

Condition(s)

Synonyms:
AllHighlyPenetrant
Identifiers:
MedGen: CN169374

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Assertion and evidence details

Submission AccessionSubmitterReview Status
(Assertion method)
Clinical Significance
(Last evaluated)
OriginMethodCitations
SCV000236800GeneDxcriteria provided, single submitter
Likely benign
(Mar 16, 2017)
germlineclinical testing

Citation Link,

SCV000713221Laboratory for Molecular Medicine, Partners HealthCare Personalized Medicinecriteria provided, single submitter
Likely benign
(Jan 18, 2019)
germlineclinical testing

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

Summary from all submissions

EthnicityOriginAffectedIndividualsFamiliesChromosomes testedNumber TestedFamily historyMethod
not providedgermlinenot provided11not providednot providednot providedclinical testing
not providedgermlineyesnot providednot providednot providednot providednot providedclinical testing

Citations

PubMed

A systematic approach to assessing the clinical significance of genetic variants.

Duzkale H, Shen J, McLaughlin H, Alfares A, Kelly MA, Pugh TJ, Funke BH, Rehm HL, Lebo MS.

Clin Genet. 2013 Nov;84(5):453-63. doi: 10.1111/cge.12257.

PubMed [citation]
PMID:
24033266
PMCID:
PMC3995020

Details of each submission

From GeneDx, SCV000236800.8

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

Description

This variant is considered likely benign or benign based on one or more of the following criteria: it is a conservative change, it occurs at a poorly conserved position in the protein, it is predicted to be benign by multiple in silico algorithms, and/or has population frequency not consistent with disease.

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

From Laboratory for Molecular Medicine, Partners HealthCare Personalized Medicine, SCV000713221.2

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not provided1not providednot providedclinical testing PubMed (1)

Description

proposed classification - variant undergoing re-assessment, contact laboratory

#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1germlinenot providednot providednot providednot provided1not provided1not provided

Last Updated: Jul 10, 2021

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