NM_001267550.2(TTN):c.105384A>G (p.Ala35128=) AND not specified

Germline classification:: Benign (6 submissions)
Last evaluated:: Aug 19, 2019
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:: RCV000040958.32

Allele description [Variation Report for NM_001267550.2(TTN):c.105384A>G (p.Ala35128=)]

NM_001267550.2(TTN):c.105384A>G (p.Ala35128=)

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.105384A>G (p.Ala35128=)

Other names:

p.A33487A:GCA>GCG

HGVS:

NC_000002.12:g.178531231T>C
NG_011618.3:g.304572A>G
NG_051363.1:g.13405T>C
NM_001256850.1:c.100461A>G
NM_001267550.2:c.105384A>GMANE SELECT
NM_003319.4:c.78189A>G
NM_133378.4:c.97680A>G
NM_133432.3:c.78564A>G
NM_133437.4:c.78765A>G
NP_001243779.1:p.Ala33487=
NP_001254479.1:p.Ala35128=
NP_001254479.2:p.Ala35128=
NP_003310.4:p.Ala26063=
NP_596869.4:p.Ala32560=
NP_597676.3:p.Ala26188=
NP_597681.4:p.Ala26255=
LRG_391t1:c.105384A>G
LRG_391:g.304572A>G
LRG_391p1:p.Ala35128=
NC_000002.11:g.179395958T>C
NM_001267550.1:c.105384A>G
NM_001267550.2:c.105384A>G
NM_133379.3:c.*214354A>G
NP_596869.4:p.(=)
c.97680A>G
p.Ala32560Ala

Links:

dbSNP: rs3813250

NCBI 1000 Genomes Browser:

rs3813250

Molecular consequence:

NM_001256850.1:c.100461A>G - synonymous variant - [Sequence Ontology: SO:0001819]
NM_001267550.2:c.105384A>G - synonymous variant - [Sequence Ontology: SO:0001819]
NM_003319.4:c.78189A>G - synonymous variant - [Sequence Ontology: SO:0001819]
NM_133378.4:c.97680A>G - synonymous variant - [Sequence Ontology: SO:0001819]
NM_133432.3:c.78564A>G - synonymous variant - [Sequence Ontology: SO:0001819]
NM_133437.4:c.78765A>G - synonymous variant - [Sequence Ontology: SO:0001819]

Observations:

924

Condition(s)

Synonyms:: AllHighlyPenetrant
Identifiers:: MedGen: CN169374

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
SCV000064649	Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine	criteria provided, single submitter (LMM Criteria)	Benign (Sep 27, 2011)	germline	clinical testing	PubMed (1) [See all records that cite this PMID]
SCV000114515	Eurofins Ntd Llc (ga)	criteria provided, single submitter (EGL Classification Definitions 2015)	Benign (Feb 12, 2016)	germline	clinical testing	Citation Link,
SCV000153437	Genetic Services Laboratory, University of Chicago	criteria provided, single submitter (ACMG Guidelines, 2007)	Benign (Aug 15, 2013)	germline	clinical testing	PubMed (1) [See all records that cite this PMID]
SCV000169476	GeneDx	criteria provided, single submitter (GeneDx Variant Classification (06012015))	Benign (Oct 31, 2012)	germline	clinical testing	Citation Link,
SCV000315651	PreventionGenetics, part of Exact Sciences	criteria provided, single submitter (ACMG Guidelines, 2015)	Benign	germline	clinical testing	PubMed (1) [See all records that cite this PMID]
SCV001360512	Women's Health and Genetics/Laboratory Corporation of America, LabCorp	criteria provided, single submitter (LabCorp Variant Classification Summary - May 2015)	Benign (Aug 19, 2019)	germline	clinical testing	Citation Link

Help

Summary from all submissions

Ethnicity	Origin	Affected	Individuals	Families	Chromosomes tested	Number Tested	Family history	Method
not provided	germline	not provided	928	924	not provided	not provided	not provided	clinical testing
not provided	germline	yes	not provided	not provided	not provided	not provided	not provided	clinical testing
	germline	unknown	6	not provided	not provided	not provided	not provided	clinical 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

ACMG recommendations for standards for interpretation and reporting of sequence variations: Revisions 2007.

Richards CS, Bale S, Bellissimo DB, Das S, Grody WW, Hegde MR, Lyon E, Ward BE; Molecular Subcommittee of the ACMG Laboratory Quality Assurance Committee.

Genet Med. 2008 Apr;10(4):294-300. doi: 10.1097/GIM.0b013e31816b5cae.

PubMed [citation]

PMID:: 18414213

See all PubMed Citations (3)

Details of each submission

From Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine, SCV000064649.6

#	Ethnicity	Individuals	Chromosomes Tested	Family History	Method	Citations
1	not provided	928	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	not provided	not provided	not provided	not provided		928	not provided	924	not provided

From Eurofins Ntd Llc (ga), SCV000114515.8

#	Ethnicity	Individuals	Chromosomes Tested	Family History	Method	Citations
1	not provided	6	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		6	not provided	not provided	not provided

From Genetic Services Laboratory, University of Chicago, SCV000153437.1

#	Ethnicity	Individuals	Chromosomes Tested	Family History	Method	Citations
1		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

From GeneDx, SCV000169476.11

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

#	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 PreventionGenetics, part of Exact Sciences, SCV000315651.1

#	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

From Women's Health and Genetics/Laboratory Corporation of America, LabCorp, SCV001360512.1

#	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	unknown	not provided	not provided	not provided		not provided	not provided	not provided	not provided

Last Updated: Nov 30, 2024

ClinVar

Relating variation to medicine