NM_003242.6(TGFBR2):c.464C>T (p.Thr155Ile) AND Familial thoracic aortic aneurysm and aortic dissection

Germline classification:: Likely benign (2 submissions)
Last evaluated:: Mar 8, 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:: RCV000777996.11

Allele description [Variation Report for NM_003242.6(TGFBR2):c.464C>T (p.Thr155Ile)]

NM_003242.6(TGFBR2):c.464C>T (p.Thr155Ile)

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.464C>T (p.Thr155Ile)

HGVS:

NC_000003.12:g.30671647C>T
NG_007490.1:g.70146C>T
NM_001024847.3:c.539C>T
NM_001407126.1:c.647C>T
NM_001407127.1:c.572C>T
NM_001407128.1:c.491C>T
NM_001407129.1:c.467C>T
NM_001407130.1:c.464C>T
NM_001407132.1:c.359C>T
NM_001407133.1:c.359C>T
NM_001407134.1:c.359C>T
NM_001407135.1:c.359C>T
NM_001407136.1:c.359C>T
NM_001407137.1:c.179C>T
NM_001407138.1:c.104C>T
NM_003242.6:c.464C>TMANE SELECT
NP_001020018.1:p.Thr180Ile
NP_001020018.1:p.Thr180Ile
NP_001394055.1:p.Thr216Ile
NP_001394056.1:p.Thr191Ile
NP_001394057.1:p.Thr164Ile
NP_001394058.1:p.Thr156Ile
NP_001394059.1:p.Thr155Ile
NP_001394061.1:p.Thr120Ile
NP_001394062.1:p.Thr120Ile
NP_001394063.1:p.Thr120Ile
NP_001394064.1:p.Thr120Ile
NP_001394065.1:p.Thr120Ile
NP_001394066.1:p.Thr60Ile
NP_001394067.1:p.Thr35Ile
NP_003233.4:p.Thr155Ile
LRG_779t1:c.539C>T
LRG_779t2:c.464C>T
LRG_779:g.70146C>T
LRG_779p1:p.Thr180Ile
LRG_779p2:p.Thr155Ile
NC_000003.11:g.30713139C>T
NM_001024847.2:c.539C>T
NM_003242.5:c.464C>T

Protein change:

T120I

Links:

dbSNP: rs727504406

NCBI 1000 Genomes Browser:

rs727504406

Molecular consequence:

NM_001024847.3:c.539C>T - missense variant - [Sequence Ontology: SO:0001583]
NM_001407126.1:c.647C>T - missense variant - [Sequence Ontology: SO:0001583]
NM_001407127.1:c.572C>T - missense variant - [Sequence Ontology: SO:0001583]
NM_001407128.1:c.491C>T - missense variant - [Sequence Ontology: SO:0001583]
NM_001407129.1:c.467C>T - missense variant - [Sequence Ontology: SO:0001583]
NM_001407130.1:c.464C>T - missense variant - [Sequence Ontology: SO:0001583]
NM_001407132.1:c.359C>T - missense variant - [Sequence Ontology: SO:0001583]
NM_001407133.1:c.359C>T - missense variant - [Sequence Ontology: SO:0001583]
NM_001407134.1:c.359C>T - missense variant - [Sequence Ontology: SO:0001583]
NM_001407135.1:c.359C>T - missense variant - [Sequence Ontology: SO:0001583]
NM_001407136.1:c.359C>T - missense variant - [Sequence Ontology: SO:0001583]
NM_001407137.1:c.179C>T - missense variant - [Sequence Ontology: SO:0001583]
NM_001407138.1:c.104C>T - missense variant - [Sequence Ontology: SO:0001583]
NM_003242.6:c.464C>T - missense variant - [Sequence Ontology: SO:0001583]

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

Recent activity

Clear Turn Off Turn On

Human nuclear transport factor 2 mRNA, complete cds
Human nuclear transport factor 2 mRNA, complete cds
gi|1167983|gb|U43939.1|HSU43939

Nucleotide
Mus musculus septin 2 (Septin2), transcript variant 6, mRNA
Mus musculus septin 2 (Septin2), transcript variant 6, mRNA
gi|2507456585|ref|NM_001421496.1|

Nucleotide

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
SCV000914103	Color Diagnostics, LLC DBA Color Health	criteria provided, single submitter (ACMG Guidelines, 2015)	Likely benign (Nov 19, 2019)	germline	clinical testing	PubMed (1) [See all records that cite this PMID]
SCV001021156	Labcorp Genetics (formerly Invitae), Labcorp	criteria provided, single submitter (Invitae Variant Classification Sherloc (09022015))	Likely benign (Mar 8, 2023)	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

SCV000914103

Color Diagnostics, LLC DBA Color Health

criteria provided, single submitter

(ACMG Guidelines, 2015)

Likely benign
(Nov 19, 2019)

germline

clinical testing

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

SCV001021156

Labcorp Genetics (formerly Invitae), Labcorp

criteria provided, single submitter

(Invitae Variant Classification Sherloc (09022015))

Likely benign
(Mar 8, 2023)

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

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

Details of each submission

From Color Diagnostics, LLC DBA Color Health, SCV000914103.2

#	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 Labcorp Genetics (formerly Invitae), Labcorp, SCV001021156.5

#	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

Last Updated: Sep 29, 2024

ClinVar

Relating variation to medicine