NM_001267550.2(TTN):c.11311+1799G>C AND not provided

Clinical significance:Likely benign (Last evaluated: Jun 24, 2013)

Review status:1 star out of maximum of 4 stars

criteria provided, single submitter

Based on:
1 submission [Details]
Record status:
current
Accession:
RCV000172721.4

Allele description [Variation Report for NM_001267550.2(TTN):c.11311+1799G>C]

NM_001267550.2(TTN):c.11311+1799G>C

Gene:
TTN:titin [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
2q31.2
Genomic location:
Preferred name:
NM_001267550.2(TTN):c.11311+1799G>C
Other names:
p.S3692T:AGT>ACT
HGVS:
  • NC_000002.12:g.178751325C>G
  • NG_011618.3:g.84478G>C
  • NM_001256850.1:c.10360+1799G>C
  • NM_001267550.2:c.11311+1799G>CMANE SELECT
  • NM_003319.4:c.10222+1799G>C
  • NM_133378.4:c.10360+1799G>C
  • NM_133379.5:c.11075G>C
  • NM_133432.3:c.10597+1799G>C
  • NM_133437.4:c.10798+1799G>C
  • NP_596870.2:p.Ser3692Thr
  • LRG_391t2:c.11075G>C
  • LRG_391:g.84478G>C
  • NC_000002.11:g.179616052C>G
  • NM_133379.3:c.11075G>C
  • NM_133379.4:c.11075G>C
  • c.11075G>C
Protein change:
S3692T
Links:
dbSNP: rs147314430
NCBI 1000 Genomes Browser:
rs147314430
Molecular consequence:
  • NM_001256850.1:c.10360+1799G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001267550.2:c.11311+1799G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_003319.4:c.10222+1799G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_133378.4:c.10360+1799G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_133432.3:c.10597+1799G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_133437.4:c.10798+1799G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_133379.5:c.11075G>C - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Identifiers:
MedGen: CN517202

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Assertion and evidence details

Submission AccessionSubmitterReview Status
(Assertion method)
Clinical Significance
(Last evaluated)
OriginMethodCitations
SCV000051330Biesecker Lab/Clinical Genomics Section,National Institutes of Health - ClinSeqcriteria provided, single submitter
Likely benign
(Jun 24, 2013)
unknownresearch

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

Description

The study set was not selected for affection status in relation to any cancer. Pathogenicity categories were based on literature curation. See Pubmed ID:23861362 for details.

SCV000051330

Medical sequencing

SCV000051330

Summary from all submissions

EthnicityOriginAffectedIndividualsFamiliesChromosomes testedNumber TestedFamily historyMethod
not providedunknownunknown3not providednot providednot providednot providedresearch

Citations

PubMed

Interpreting secondary cardiac disease variants in an exome cohort.

Ng D, Johnston JJ, Teer JK, Singh LN, Peller LC, Wynter JS, Lewis KL, Cooper DN, Stenson PD, Mullikin JC, Biesecker LG; NIH Intramural Sequencing Center (NISC) Comparative Sequencing Program..

Circ Cardiovasc Genet. 2013 Aug;6(4):337-46. doi: 10.1161/CIRCGENETICS.113.000039. Epub 2013 Jul 16.

PubMed [citation]
PMID:
23861362
PMCID:
PMC3887521

Details of each submission

From Biesecker Lab/Clinical Genomics Section,National Institutes of Health - ClinSeq, SCV000051330.1

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not provided3not providednot providedresearch PubMed (1)
#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1unknownunknownnot providednot providednot provided3not providednot providednot provided

Last Updated: Sep 6, 2021

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