NM_001267550.2(TTN):c.18037T>C (p.Tyr6013His) AND Cardiomyopathy

Germline classification:: Uncertain significance (1 submission)
Last evaluated:: Jan 9, 2017
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:: RCV000769074.10

Allele description [Variation Report for NM_001267550.2(TTN):c.18037T>C (p.Tyr6013His)]

NM_001267550.2(TTN):c.18037T>C (p.Tyr6013His)

Gene:

TTN:titin [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

2q31.2

Genomic location:

Preferred name:

NM_001267550.2(TTN):c.18037T>C (p.Tyr6013His)

Other names:

p.Y5696H:TAC>CAC

HGVS:

NC_000002.12:g.178730363A>G
NG_011618.3:g.105440T>C
NM_001256850.1:c.17086T>C
NM_001267550.2:c.18037T>CMANE SELECT
NM_003319.4:c.13282+7719T>C
NM_133378.4:c.14305T>C
NM_133432.3:c.13657+7719T>C
NM_133437.4:c.13858+7719T>C
NP_001243779.1:p.Tyr5696His
NP_001254479.2:p.Tyr6013His
NP_596869.4:p.Tyr4769His
LRG_391:g.105440T>C
NC_000002.11:g.179595090A>G
NM_001267550.1:c.18037T>C
p.Tyr4769His

Protein change:

Y4769H

Links:

dbSNP: rs548015673

NCBI 1000 Genomes Browser:

rs548015673

Molecular consequence:

NM_003319.4:c.13282+7719T>C - intron variant - [Sequence Ontology: SO:0001627]
NM_133432.3:c.13657+7719T>C - intron variant - [Sequence Ontology: SO:0001627]
NM_133437.4:c.13858+7719T>C - intron variant - [Sequence Ontology: SO:0001627]
NM_001256850.1:c.17086T>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001267550.2:c.18037T>C - missense variant - [Sequence Ontology: SO:0001583]
NM_133378.4:c.14305T>C - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Name:: Cardiomyopathy (CMYO)
Synonyms:: Cardiomyopathies
Identifiers:: MONDO: MONDO:0004994; MedGen: C0878544; Human Phenotype Ontology: HP:0001638

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV000900447	CHEO Genetics Diagnostic Laboratory, Children's Hospital of Eastern Ontario - Canadian Open Genetics Repository	criteria provided, single submitter (ACMG Guidelines, 2015)	Uncertain significance (Jan 9, 2017)	germline	clinical testing	PubMed (1) [See all records that cite this PMID]

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV000900447

CHEO Genetics Diagnostic Laboratory, Children's Hospital of Eastern Ontario - Canadian Open Genetics Repository

criteria provided, single submitter

(ACMG Guidelines, 2015)

Uncertain significance
(Jan 9, 2017)

germline

clinical testing

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

Help

Summary from all submissions

Ethnicity	Origin	Affected	Individuals	Families	Chromosomes tested	Number Tested	Family history	Method
not provided	germline	unknown	not provided	not provided	not provided	not provided	not provided	clinical testing

Citations

PubMed

Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology.

Richards S, Aziz N, Bale S, Bick D, Das S, Gastier-Foster J, Grody WW, Hegde M, Lyon E, Spector E, Voelkerding K, Rehm HL; ACMG Laboratory Quality Assurance Committee.

Genet Med. 2015 May;17(5):405-24. doi: 10.1038/gim.2015.30. Epub 2015 Mar 5.

PubMed [citation]

PMID:: 25741868
PMCID:: PMC4544753

Details of each submission

From CHEO Genetics Diagnostic Laboratory, Children's Hospital of Eastern Ontario - Canadian Open Genetics Repository, SCV000900447.1

#	Ethnicity	Individuals	Chromosomes Tested	Family History	Method	Citations
1	not provided	not provided	not provided	not provided	clinical testing	PubMed (1)

#	Sample				Method		Observation
#	Origin	Affected	Number tested	Tissue	Purpose	Method	Individuals	Allele frequency	Families	Co-occurrences
1	germline	unknown	not provided	not provided	not provided		not provided	not provided	not provided	not provided

Last Updated: Nov 24, 2024

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