NM_001267550.2(TTN):c.10100G>A (p.Arg3367Gln) AND not provided

Germline classification:: Benign/Likely benign (4 submissions)
Last evaluated:: Oct 2, 2023
Review status:: 2 stars out of maximum of 4 stars
criteria provided, multiple submitters, no conflicts

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:: RCV001528575.20

Allele description [Variation Report for NM_001267550.2(TTN):c.10100G>A (p.Arg3367Gln)]

NM_001267550.2(TTN):c.10100G>A (p.Arg3367Gln)

Gene:

TTN:titin [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

2q31.2

Genomic location:

Preferred name:

NM_001267550.2(TTN):c.10100G>A (p.Arg3367Gln)

Other names:

p.R3367Q:CGG>CAG

HGVS:

NC_000002.12:g.178764191C>T
NG_011618.3:g.71612G>A
NM_001256850.1:c.10100G>A
NM_001267550.2:c.10100G>AMANE SELECT
NM_003319.4:c.9962G>A
NM_133378.4:c.10100G>A
NM_133379.5:c.10100G>A
NM_133432.3:c.9962G>A
NM_133437.4:c.9962G>A
NP_001243779.1:p.Arg3367Gln
NP_001254479.2:p.Arg3367Gln
NP_003310.4:p.Arg3321Gln
NP_596869.4:p.Arg3367Gln
NP_596870.2:p.Arg3367Gln
NP_597676.3:p.Arg3321Gln
NP_597681.4:p.Arg3321Gln
LRG_391:g.71612G>A
NC_000002.11:g.179628918C>T
NM_001267550.1:c.10100G>A
Q8WZ42:p.Arg3367Gln
c.10100G>A

Protein change:

R3321Q

Links:

UniProtKB: Q8WZ42#VAR_040123; dbSNP: rs34819099

NCBI 1000 Genomes Browser:

rs34819099

Molecular consequence:

NM_001256850.1:c.10100G>A - missense variant - [Sequence Ontology: SO:0001583]
NM_001267550.2:c.10100G>A - missense variant - [Sequence Ontology: SO:0001583]
NM_003319.4:c.9962G>A - missense variant - [Sequence Ontology: SO:0001583]
NM_133378.4:c.10100G>A - missense variant - [Sequence Ontology: SO:0001583]
NM_133379.5:c.10100G>A - missense variant - [Sequence Ontology: SO:0001583]
NM_133432.3:c.9962G>A - missense variant - [Sequence Ontology: SO:0001583]
NM_133437.4:c.9962G>A - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Synonyms:: none provided
Identifiers:: MedGen: C3661900

Recent activity

Clear Turn Off Turn On

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

Help

Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV001473125	ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories	criteria provided, single submitter (ARUP Molecular Germline Variant Investigation Process 2024)	Benign (Oct 2, 2023)	germline	clinical testing	Citation Link,
SCV001740514	Diagnostic Laboratory, Department of Genetics, University Medical Center Groningen - VKGL Data-share Consensus	no assertion criteria provided	Likely benign	germline	clinical testing
SCV001800293	Laboratory of Diagnostic Genome Analysis, Leiden University Medical Center (LUMC) - VKGL Data-share Consensus	no assertion criteria provided	Likely benign	germline	clinical testing
SCV005260134	Breakthrough Genomics, Breakthrough Genomics	criteria provided, single submitter (ACMG Guidelines, 2015)	Likely benign	germline	not provided	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	yes	not provided	not provided	not provided	not provided	not provided	clinical testing, not provided
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 ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories, SCV001473125.5

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

#	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

From Diagnostic Laboratory, Department of Genetics, University Medical Center Groningen - VKGL Data-share Consensus, SCV001740514.3

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

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

From Laboratory of Diagnostic Genome Analysis, Leiden University Medical Center (LUMC) - VKGL Data-share Consensus, SCV001800293.1

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

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

From Breakthrough Genomics, Breakthrough Genomics, SCV005260134.1

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

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

Last Updated: Nov 10, 2024

ClinVar

Relating variation to medicine