rs61762550

Variant names:

Your query was ambiguous. Multiple possible variants found:

Variant summary

Our verdict is Benign. The variant received -9 ACMG points: 0P and 9B. BP4_ModerateBP6_ModerateBP7BS2

The NM_003242.6(TGFBR2):c.577C>A(p.Arg193Arg) variant causes a synonymous change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.00000889 in 1,461,882 control chromosomes in the GnomAD database, with no homozygous occurrence. In-silico tool predicts a benign outcome for this variant. Variant has been reported in ClinVar as Likely benign (★).

Frequency

Genomes: not found (cov: 33)

Exomes 𝑓: 0.0000089 ( 0 hom. )

Consequence

TGFBR2
NM_003242.6 synonymous

Scores

Clinical Significance

Likely benign criteria provided, single submitter B:1

Conservation

PhyloP100: 2.40

Publications

11 publications found

Variant links:

Genes affected

TGFBR2 (HGNC:11773): (transforming growth factor beta receptor 2) The protein encoded by this gene is a transmembrane protein that has a protein kinase domain, forms a heterodimeric complex with TGF-beta receptor type-1, and binds TGF-beta. This receptor/ligand complex phosphorylates proteins, which then enter the nucleus and regulate the transcription of genes related to cell proliferation, cell cycle arrest, wound healing, immunosuppression, and tumorigenesis. Mutations in this gene have been associated with Marfan Syndrome, Loeys-Deitz Aortic Aneurysm Syndrome, and the development of various types of tumors. Alternatively spliced transcript variants encoding different isoforms have been characterized. [provided by RefSeq, Aug 2017]

TGFBR2 Gene-Disease associations (from GenCC):

familial thoracic aortic aneurysm and aortic dissection
Inheritance: AD Classification: DEFINITIVE, SUPPORTIVE Submitted by: ClinGen, Orphanet
Loeys-Dietz syndrome 2
Inheritance: AD Classification: DEFINITIVE, STRONG Submitted by: ClinGen, Labcorp Genetics (formerly Invitae), PanelApp Australia, Genomics England PanelApp, G2P
Loeys-Dietz syndrome
Inheritance: AD Classification: SUPPORTIVE Submitted by: Orphanet

TGFBR2 links:

Genome browser will be placed here

ACMG classification

Classification was made for transcript

Our verdict: Benign. The variant received -9 ACMG points.

BP4

Computational evidence support a benign effect (BayesDel_noAF=-0.28).

BP6

Variant 3-30671760-C-A is Benign according to our data. Variant chr3-30671760-C-A is described in CliVar as Likely_benign. Clinvar id is 2730178.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chr3-30671760-C-A is described in CliVar as Likely_benign. Clinvar id is 2730178.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chr3-30671760-C-A is described in CliVar as Likely_benign. Clinvar id is 2730178.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chr3-30671760-C-A is described in CliVar as Likely_benign. Clinvar id is 2730178.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chr3-30671760-C-A is described in CliVar as Likely_benign. Clinvar id is 2730178.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chr3-30671760-C-A is described in CliVar as Likely_benign. Clinvar id is 2730178.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chr3-30671760-C-A is described in CliVar as Likely_benign. Clinvar id is 2730178.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chr3-30671760-C-A is described in CliVar as Likely_benign. Clinvar id is 2730178.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chr3-30671760-C-A is described in CliVar as Likely_benign. Clinvar id is 2730178.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chr3-30671760-C-A is described in CliVar as Likely_benign. Clinvar id is 2730178.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chr3-30671760-C-A is described in CliVar as Likely_benign. Clinvar id is 2730178.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chr3-30671760-C-A is described in CliVar as Likely_benign. Clinvar id is 2730178.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chr3-30671760-C-A is described in CliVar as Likely_benign. Clinvar id is 2730178.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chr3-30671760-C-A is described in CliVar as Likely_benign. Clinvar id is 2730178.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chr3-30671760-C-A is described in CliVar as Likely_benign. Clinvar id is 2730178.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chr3-30671760-C-A is described in CliVar as Likely_benign. Clinvar id is 2730178.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chr3-30671760-C-A is described in CliVar as Likely_benign. Clinvar id is 2730178.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chr3-30671760-C-A is described in CliVar as Likely_benign. Clinvar id is 2730178.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chr3-30671760-C-A is described in CliVar as Likely_benign. Clinvar id is 2730178.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chr3-30671760-C-A is described in CliVar as Likely_benign. Clinvar id is 2730178.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chr3-30671760-C-A is described in CliVar as Likely_benign. Clinvar id is 2730178.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chr3-30671760-C-A is described in CliVar as Likely_benign. Clinvar id is 2730178.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chr3-30671760-C-A is described in CliVar as Likely_benign. Clinvar id is 2730178.Status of the report is criteria_provided_single_submitter, 1 stars.

BP7

Synonymous conserved (PhyloP=2.4 with no splicing effect.

BS2

High AC in GnomAdExome4 at 13 AD gene.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
TGFBR2	NM_003242.6 link	c.577C>A	p.Arg193Arg	synonymous_variant	Exon 4 of 7	ENST00000295754.10	NP_003233.4	P37173-1A3QNQ0

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
TGFBR2	ENST00000295754.10 link	c.577C>A	p.Arg193Arg	synonymous_variant	Exon 4 of 7	1	NM_003242.6	ENSP00000295754.5		P37173-1

Frequencies

GnomAD3 genomes

Cov.:

GnomAD2 exomes

AF:

0.00000398

AC:

AN:

251190

AF XY:

0.00000737

show subpopulations

Gnomad AFR exome

AF:

0.00

Gnomad AMR exome

AF:

0.00

Gnomad ASJ exome

AF:

0.00

Gnomad EAS exome

AF:

0.00

Gnomad FIN exome

AF:

0.00

Gnomad NFE exome

AF:

0.00000881

Gnomad OTH exome

AF:

0.00

GnomAD4 exome

AF:

0.00000889

AC:

AN:

1461882

Hom.:

Cov.:

AF XY:

0.00000275

AC XY:

AN XY:

727244

show subpopulations

African (AFR)

AF:

0.00

AC:

AN:

33480

American (AMR)

AF:

0.00

AC:

AN:

44724

Ashkenazi Jewish (ASJ)

AF:

0.00

AC:

AN:

26136

East Asian (EAS)

AF:

0.00

AC:

AN:

39700

South Asian (SAS)

AF:

0.00

AC:

AN:

86258

European-Finnish (FIN)

AF:

0.00

AC:

AN:

53420

Middle Eastern (MID)

AF:

0.00

AC:

AN:

5768

European-Non Finnish (NFE)

AF:

0.0000117

AC:

AN:

1112000

Other (OTH)

AF:

0.00

AC:

AN:

60396

Allele Balance Distribution

Red line indicates average allele balance

Average allele balance: 0.479

Heterozygous variant carriers

0.00

0.20

0.40

0.60

0.80

0.95

Allele balance

Age Distribution

Exome Het

Variant carriers

<30

30-35

35-40

40-45

45-50

50-55

55-60

60-65

65-70

70-75

75-80

>80

Age

GnomAD4 genome

Cov.:

Alfa

AF:

0.00

Hom.:

Bravo

AF:

0.00000378

ClinVar

Significance: Likely benign

Submissions summary: Benign:1

Revision: criteria provided, single submitter

LINK: link

Submissions by phenotype

Familial thoracic aortic aneurysm and aortic dissection

Benign:1

Dec 11, 2023

Labcorp Genetics (formerly Invitae), Labcorp

Significance:Likely benign

Review Status:criteria provided, single submitter

Collection Method:clinical testing

- -

Computational scores

Source: dbNSFP v4.3

Name

Calibrated prediction

Score

Prediction

BayesDel_noAF

Benign

-0.28

CADD

Benign

(source)

DANN

Benign

0.71

PhyloP100

2.4

RBP_binding_hub_radar

0.0

RBP_regulation_power_radar

1.7

Splicing

Name

Calibrated prediction

Score

Prediction

SpliceAI score (max)

0.090

Details are displayed if max score is > 0.2

Find out detailed SpliceAI scores and Pangolin per-transcript scores at spliceailookup.broadinstitute.org

Publications

You must be logged in to view publications. This limit was set because tens of millions (!) of queries from AI bots are generated daily.

Variant summary

Frequency

Consequence

Scores

Clinical Significance

Conservation

Publications

ACMG classification

Transcripts

RefSeq

Ensembl

Frequencies

Age Distribution

ClinVar

Submissions by phenotype

Computational scores

Splicing

Publications

Other links and lift over