NM_003242.6(TGFBR2):c.690G>A (p.Thr230=) AND Familial thoracic aortic aneurysm and aortic dissection

Germline classification:: Conflicting interpretations of pathogenicity (5 submissions)
Last evaluated:: Dec 19, 2023
Review status:: criteria provided, conflicting classifications

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:: RCV000266417.27

Allele description [Variation Report for NM_003242.6(TGFBR2):c.690G>A (p.Thr230=)]

NM_003242.6(TGFBR2):c.690G>A (p.Thr230=)

Gene:

TGFBR2:transforming growth factor beta receptor 2 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

3p24.1

Genomic location:

Preferred name:

NM_003242.6(TGFBR2):c.690G>A (p.Thr230=)

HGVS:

NC_000003.12:g.30671873G>A
NG_007490.1:g.70372G>A
NM_001024847.3:c.765G>A
NM_001407126.1:c.873G>A
NM_001407127.1:c.798G>A
NM_001407128.1:c.717G>A
NM_001407129.1:c.693G>A
NM_001407130.1:c.690G>A
NM_001407132.1:c.585G>A
NM_001407133.1:c.585G>A
NM_001407134.1:c.585G>A
NM_001407135.1:c.585G>A
NM_001407136.1:c.585G>A
NM_001407137.1:c.405G>A
NM_001407138.1:c.330G>A
NM_001407139.1:c.530-16514G>A
NM_003242.6:c.690G>AMANE SELECT
NP_001020018.1:p.Thr255=
NP_001020018.1:p.Thr255=
NP_001394055.1:p.Thr291=
NP_001394056.1:p.Thr266=
NP_001394057.1:p.Thr239=
NP_001394058.1:p.Thr231=
NP_001394059.1:p.Thr230=
NP_001394061.1:p.Thr195=
NP_001394062.1:p.Thr195=
NP_001394063.1:p.Thr195=
NP_001394064.1:p.Thr195=
NP_001394065.1:p.Thr195=
NP_001394066.1:p.Thr135=
NP_001394067.1:p.Thr110=
NP_003233.4:p.Thr230=
LRG_779t1:c.765G>A
LRG_779t2:c.690G>A
LRG_779:g.70372G>A
LRG_779p1:p.Thr255=
LRG_779p2:p.Thr230=
NC_000003.11:g.30713365G>A
NM_001024847.2:c.765G>A
NM_003242.5:c.690G>A

Links:

dbSNP: rs201560560

NCBI 1000 Genomes Browser:

rs201560560

Molecular consequence:

NM_001407139.1:c.530-16514G>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001024847.3:c.765G>A - synonymous variant - [Sequence Ontology: SO:0001819]
NM_001407126.1:c.873G>A - synonymous variant - [Sequence Ontology: SO:0001819]
NM_001407127.1:c.798G>A - synonymous variant - [Sequence Ontology: SO:0001819]
NM_001407128.1:c.717G>A - synonymous variant - [Sequence Ontology: SO:0001819]
NM_001407129.1:c.693G>A - synonymous variant - [Sequence Ontology: SO:0001819]
NM_001407130.1:c.690G>A - synonymous variant - [Sequence Ontology: SO:0001819]
NM_001407132.1:c.585G>A - synonymous variant - [Sequence Ontology: SO:0001819]
NM_001407133.1:c.585G>A - synonymous variant - [Sequence Ontology: SO:0001819]
NM_001407134.1:c.585G>A - synonymous variant - [Sequence Ontology: SO:0001819]
NM_001407135.1:c.585G>A - synonymous variant - [Sequence Ontology: SO:0001819]
NM_001407136.1:c.585G>A - synonymous variant - [Sequence Ontology: SO:0001819]
NM_001407137.1:c.405G>A - synonymous variant - [Sequence Ontology: SO:0001819]
NM_001407138.1:c.330G>A - synonymous variant - [Sequence Ontology: SO:0001819]
NM_003242.6:c.690G>A - synonymous variant - [Sequence Ontology: SO:0001819]

Condition(s)

Name:: Familial thoracic aortic aneurysm and aortic dissection (TAAD)
Synonyms:: Thoracic aortic aneurysm and aortic dissection; Thoracic aortic aneurysms and dissections
Identifiers:: MONDO: MONDO:0019625; MedGen: C4707243; Orphanet: 91387; OMIM: PS607086

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gi|1130413394|ref|NM_010861.4|

Nucleotide
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MFNG [Equus asinus]
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Gene ID:106837591

Gene

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV000442851	Illumina Laboratory Services, Illumina	criteria provided, single submitter (ICSL Variant Classification 20161018)	Uncertain significance (Jun 14, 2016)	germline	clinical testing	ICSL_Variant_Classification_20161018.pdf, Citation Link,
SCV001007059	Labcorp Genetics (formerly Invitae), Labcorp	criteria provided, single submitter (Invitae Variant Classification Sherloc (09022015))	Benign (Dec 19, 2023)	germline	clinical testing	PubMed (1) [See all records that cite this PMID]
SCV001353190	Color Diagnostics, LLC DBA Color Health	criteria provided, single submitter (ACMG Guidelines, 2015)	Likely benign (Jan 7, 2019)	germline	clinical testing	PubMed (1) [See all records that cite this PMID]
SCV002042884	CHEO Genetics Diagnostic Laboratory, Children's Hospital of Eastern Ontario	criteria provided, single submitter (ACMG Guidelines, 2015)	Likely benign (Nov 19, 2020)	germline	clinical testing	PubMed (1) [See all records that cite this PMID]
SCV002668185	Ambry Genetics	criteria provided, single submitter (Ambry Variant Classification Scheme 2023)	Likely benign (Mar 30, 2018)	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	unknown	not provided	not provided	not provided	not provided	not provided	clinical testing

Citations

PubMed

Sherloc: a comprehensive refinement of the ACMG-AMP variant classification criteria.

Nykamp K, Anderson M, Powers M, Garcia J, Herrera B, Ho YY, Kobayashi Y, Patil N, Thusberg J, Westbrook M; Invitae Clinical Genomics Group., Topper S.

Genet Med. 2017 Oct;19(10):1105-1117. doi: 10.1038/gim.2017.37. Epub 2017 May 11. Erratum in: Genet Med. 2020 Jan;22(1):240. doi: 10.1038/s41436-019-0624-9.

PubMed [citation]

PMID:: 28492532
PMCID:: PMC5632818

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 Illumina Laboratory Services, Illumina, SCV000442851.2

#	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 Labcorp Genetics (formerly Invitae), Labcorp, SCV001007059.5

#	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 Color Diagnostics, LLC DBA Color Health, SCV001353190.1

#	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 CHEO Genetics Diagnostic Laboratory, Children's Hospital of Eastern Ontario, SCV002042884.1

#	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 Ambry Genetics, SCV002668185.2

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

Description

This alteration is classified as likely benign based on a combination of the following: seen in unaffected individuals, 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.

#	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 3, 2024

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