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NM_001267550.2(TTN):c.22080T>C (p.Asp7360=) AND Cardiovascular phenotype

Germline classification:
Benign (1 submission)
Last evaluated:
Jan 16, 2013
Review status:
1 star out of maximum of 4 stars
criteria provided, single submitter
Somatic classification
of clinical impact:
None
Review status:
(0/4) 0 stars out of maximum of 4 stars
no assertion criteria provided
Somatic classification
of oncogenicity:
None
Review status:
(0/4) 0 stars out of maximum of 4 stars
no assertion criteria provided
Record status:
current
Accession:
RCV000248980.9

Allele description [Variation Report for NM_001267550.2(TTN):c.22080T>C (p.Asp7360=)]

NM_001267550.2(TTN):c.22080T>C (p.Asp7360=)

Gene:
TTN:titin [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
2q31.2
Genomic location:
Preferred name:
NM_001267550.2(TTN):c.22080T>C (p.Asp7360=)
Other names:
p.D6116D:GAT>GAC
HGVS:
  • NC_000002.12:g.178722819A>G
  • NG_011618.3:g.112984T>C
  • NM_001256850.1:c.21129T>C
  • NM_001267550.2:c.22080T>CMANE SELECT
  • NM_003319.4:c.13282+15263T>C
  • NM_133378.4:c.18348T>C
  • NM_133432.3:c.13657+15263T>C
  • NM_133437.4:c.13858+15263T>C
  • NP_001243779.1:p.Asp7043=
  • NP_001254479.1:p.Asp7360=
  • NP_001254479.2:p.Asp7360=
  • NP_596869.4:p.Asp6116=
  • LRG_391t1:c.22080T>C
  • LRG_391:g.112984T>C
  • LRG_391p1:p.Asp7360=
  • NC_000002.11:g.179587546A>G
  • NM_001267550.1:c.22080T>C
  • NM_001267550.2:c.22080T>C
  • NM_133379.3:c.*22766T>C
  • c.18348T>C
  • p.Asp6116Asp
Links:
dbSNP: rs16866473
NCBI 1000 Genomes Browser:
rs16866473
Molecular consequence:
  • NM_003319.4:c.13282+15263T>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_133432.3:c.13657+15263T>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_133437.4:c.13858+15263T>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001256850.1:c.21129T>C - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001267550.2:c.22080T>C - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_133378.4:c.18348T>C - synonymous variant - [Sequence Ontology: SO:0001819]
Observations:
1

Condition(s)

Name:
Cardiovascular phenotype
Identifiers:
MedGen: CN230736

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Assertion and evidence details

Help
Submission AccessionSubmitterReview Status
(Assertion method)		Clinical Significance
(Last evaluated)		OriginMethodCitations
SCV000317940Ambry Genetics
criteria provided, single submitter

(Ambry Autosomal Dominant and X-Linked criteria (10/2015))		Benign
(Jan 16, 2013) 		germlineclinical testing

Citation Link

Help

Summary from all submissions

EthnicityOriginAffectedIndividualsFamiliesChromosomes testedNumber TestedFamily historyMethod
not providedgermlineunknown1not providednot provided1not providedclinical testing

Details of each submission

From Ambry Genetics, SCV000317940.5

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not provided1not providednot providedclinical testingnot provided

Description

This alteration is classified as benign based on a combination of the following: population frequency, intact protein function, lack of segregation with disease, co-occurrence, RNA analysis, in silico models, amino acid conservation, lack of disease association in case-control studies, and/or the mechanism of disease or impacted region is inconsistent with a known cause of pathogenicity.

#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1germlineunknown1not providednot provided1not providednot providednot provided

Last Updated: Jan 4, 2025