rs371221124

Variant names:

Variant summary

Our verdict is Benign. The variant received -21 ACMG points: 0P and 21B. BP4_StrongBP6_Very_StrongBP7BS1BS2

The NM_003242.6(TGFBR2):c.567C>T(p.Tyr189Tyr) variant causes a synonymous change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.0000712 in 1,614,104 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: 𝑓 0.000046 ( 0 hom., cov: 33)

Exomes 𝑓: 0.000074 ( 0 hom. )

Consequence

TGFBR2
NM_003242.6 synonymous

Scores

Clinical Significance

Likely benign criteria provided, multiple submitters, no conflicts B:7

Conservation

PhyloP100: 2.00

Publications

2 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 -21 ACMG points.

BP4

Computational evidence support a benign effect (BayesDel_noAF=-0.62).

BP6

Variant 3-30671750-C-T is Benign according to our data. Variant chr3-30671750-C-T is described in CliVar as Likely_benign. Clinvar id is 543909.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr3-30671750-C-T is described in CliVar as Likely_benign. Clinvar id is 543909.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr3-30671750-C-T is described in CliVar as Likely_benign. Clinvar id is 543909.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr3-30671750-C-T is described in CliVar as Likely_benign. Clinvar id is 543909.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr3-30671750-C-T is described in CliVar as Likely_benign. Clinvar id is 543909.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr3-30671750-C-T is described in CliVar as Likely_benign. Clinvar id is 543909.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr3-30671750-C-T is described in CliVar as Likely_benign. Clinvar id is 543909.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr3-30671750-C-T is described in CliVar as Likely_benign. Clinvar id is 543909.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr3-30671750-C-T is described in CliVar as Likely_benign. Clinvar id is 543909.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr3-30671750-C-T is described in CliVar as Likely_benign. Clinvar id is 543909.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr3-30671750-C-T is described in CliVar as Likely_benign. Clinvar id is 543909.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr3-30671750-C-T is described in CliVar as Likely_benign. Clinvar id is 543909.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr3-30671750-C-T is described in CliVar as Likely_benign. Clinvar id is 543909.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr3-30671750-C-T is described in CliVar as Likely_benign. Clinvar id is 543909.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr3-30671750-C-T is described in CliVar as Likely_benign. Clinvar id is 543909.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr3-30671750-C-T is described in CliVar as Likely_benign. Clinvar id is 543909.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr3-30671750-C-T is described in CliVar as Likely_benign. Clinvar id is 543909.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr3-30671750-C-T is described in CliVar as Likely_benign. Clinvar id is 543909.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr3-30671750-C-T is described in CliVar as Likely_benign. Clinvar id is 543909.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr3-30671750-C-T is described in CliVar as Likely_benign. Clinvar id is 543909.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr3-30671750-C-T is described in CliVar as Likely_benign. Clinvar id is 543909.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr3-30671750-C-T is described in CliVar as Likely_benign. Clinvar id is 543909.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr3-30671750-C-T is described in CliVar as Likely_benign. Clinvar id is 543909.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars.

BP7

Synonymous conserved (PhyloP=2 with no splicing effect.

BS1

Variant frequency is greater than expected in population nfe. GnomAdExome4 allele frequency = 0.0000739 (108/1461882) while in subpopulation NFE AF = 0.0000917 (102/1112000). AF 95% confidence interval is 0.0000769. There are 0 homozygotes in GnomAdExome4. There are 59 alleles in the male GnomAdExome4 subpopulation. Median coverage is 34. This position passed quality control check.

BS2

High AC in GnomAd4 at 7 AD gene.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
TGFBR2	NM_003242.6 link	c.567C>T	p.Tyr189Tyr	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.567C>T	p.Tyr189Tyr	synonymous_variant	Exon 4 of 7	1	NM_003242.6	ENSP00000295754.5		P37173-1

Frequencies

GnomAD3 genomes

AF:

0.0000460

AC:

AN:

152222

Hom.:

Cov.:

show subpopulations

Gnomad AFR

AF:

0.0000965

Gnomad AMI

AF:

0.00

Gnomad AMR

AF:

0.00

Gnomad ASJ

AF:

0.00

Gnomad EAS

AF:

0.00

Gnomad SAS

AF:

0.00

Gnomad FIN

AF:

0.00

Gnomad MID

AF:

0.00

Gnomad NFE

AF:

0.0000441

Gnomad OTH

AF:

0.00

GnomAD2 exomes

AF:

0.0000119

AC:

AN:

251232

AF XY:

0.0000147

show subpopulations

Gnomad AFR exome

AF:

0.0000615

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:

0.0000176

Gnomad OTH exome

AF:

0.00

GnomAD4 exome

AF:

0.0000739

AC:

108

AN:

1461882

Hom.:

Cov.:

AF XY:

0.0000811

AC XY:

AN XY:

727244

show subpopulations

African (AFR)

AF:

0.0000597

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:

0.0000917

AC:

102

AN:

1112000

Other (OTH)

AF:

0.0000662

AC:

AN:

60396

Allele Balance Distribution

Red line indicates average allele balance

Average allele balance: 0.473

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

AF:

0.0000460

AC:

AN:

152222

Hom.:

Cov.:

AF XY:

0.0000403

AC XY:

AN XY:

74354

show subpopulations

African (AFR)

AF:

0.0000965

AC:

AN:

41460

American (AMR)

AF:

0.00

AC:

AN:

15284

Ashkenazi Jewish (ASJ)

AF:

0.00

AC:

AN:

3472

East Asian (EAS)

AF:

0.00

AC:

AN:

5190

South Asian (SAS)

AF:

0.00

AC:

AN:

4834

European-Finnish (FIN)

AF:

0.00

AC:

AN:

10620

Middle Eastern (MID)

AF:

0.00

AC:

AN:

316

European-Non Finnish (NFE)

AF:

0.0000441

AC:

AN:

68040

Other (OTH)

AF:

0.00

AC:

AN:

2094

Allele Balance Distribution

Red line indicates average allele balance

Average allele balance: 0.525

Heterozygous variant carriers

0.00

0.20

0.40

0.60

0.80

0.95

Allele balance

Age Distribution

Genome 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

Alfa

AF:

0.0000282

Hom.:

Bravo

AF:

0.0000340

EpiCase

AF:

0.0000545

EpiControl

AF:

0.00

ClinVar

Significance: Likely benign

Submissions summary: Benign:7

Revision: criteria provided, multiple submitters, no conflicts

LINK: link

Submissions by phenotype

Familial thoracic aortic aneurysm and aortic dissection

Benign:3

Feb 25, 2019

Color Diagnostics, LLC DBA Color Health

Significance:Likely benign

Review Status:criteria provided, single submitter

Collection Method:clinical testing

- -

Feb 29, 2016

Ambry Genetics

Significance:Likely benign

Review Status:criteria provided, single submitter

Collection Method:clinical testing

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. -

Jan 15, 2025

Labcorp Genetics (formerly Invitae), Labcorp

Significance:Likely benign

Review Status:criteria provided, single submitter

Collection Method:clinical testing

- -

not specified

Benign:1

Oct 15, 2019

Women's Health and Genetics/Laboratory Corporation of America, LabCorp

Significance:Likely benign

Review Status:criteria provided, single submitter

Collection Method:clinical testing

- -

not provided

Benign:1

Jun 22, 2021

GeneDx

Significance:Likely benign

Review Status:criteria provided, single submitter

Collection Method:clinical testing

- -

Loeys-Dietz syndrome 2

Benign:1

Nov 20, 2023

All of Us Research Program, National Institutes of Health

Significance:Likely benign

Review Status:criteria provided, single submitter

Collection Method:clinical testing

- -

TGFBR2-related disorder

Benign:1

Jan 23, 2024

PreventionGenetics, part of Exact Sciences

Significance:Likely benign

Review Status:no assertion criteria provided

Collection Method:clinical testing

This variant is classified as likely benign based on ACMG/AMP sequence variant interpretation guidelines (Richards et al. 2015 PMID: 25741868, with internal and published modifications). -

Computational scores

Source: dbNSFP v4.3

Name

Calibrated prediction

Score

Prediction

BayesDel_noAF

Benign

-0.62

CADD

Benign

6.0

(source)

DANN

Benign

0.52

PhyloP100

2.0

RBP_binding_hub_radar

0.0

RBP_regulation_power_radar

1.7

Mutation Taster

=93/7

polymorphism

(source)

Splicing

Name

Calibrated prediction

Score

Prediction

SpliceAI score (max)

0.0

Details are displayed if max score is > 0.2

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

Publications

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Variant summary

Frequency

Consequence

Scores

Clinical Significance

Conservation

Publications

ACMG classification

Transcripts

RefSeq

Ensembl

Frequencies

Age Distribution

Age Distribution

ClinVar

Submissions by phenotype

Computational scores

Splicing

Publications

Other links and lift over