rs2796813

Positions:

• chr1-218415855-T-C

Variant summary

Our verdict is Benign. Variant got -12 ACMG points: 0P and 12B. BP4_Strong BA1

The NM_003238.6(TGFB2):​c.510+10523T>C variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.586 in 151,668 control chromosomes in the GnomAD database, including 29,011 homozygotes. In-silico tool predicts a benign outcome for this variant. No clinical diagnostic laboratories have submitted clinical-significance assessments for this variant to ClinVar.

• Frequency: Genomes: 𝑓 0.59 (29011 hom., cov: 30)
• Consequence: TGFB2 NM_003238.6 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -4.49

Genes affected

TGFB2 (HGNC:11768): (transforming growth factor beta 2) This gene encodes a secreted ligand of the TGF-beta (transforming growth factor-beta) superfamily of proteins. Ligands of this family bind various TGF-beta receptors leading to recruitment and activation of SMAD family transcription factors that regulate gene expression. The encoded preproprotein is proteolytically processed to generate a latency-associated peptide (LAP) and a mature peptide, and is found in either a latent form composed of a mature peptide homodimer, a LAP homodimer, and a latent TGF-beta binding protein, or in an active form consisting solely of the mature peptide homodimer. The mature peptide may also form heterodimers with other TGF-beta family members. Disruption of the TGF-beta/SMAD pathway has been implicated in a variety of human cancers. A chromosomal translocation that includes this gene is associated with Peters' anomaly, a congenital defect of the anterior chamber of the eye. Mutations in this gene may be associated with Loeys-Dietz syndrome. This gene encodes multiple isoforms that may undergo similar proteolytic processing. [provided by RefSeq, Aug 2016]

ACMG classification

Verdict is Benign. Variant got -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.91).
• BA1: GnomAd4 highest subpopulation (AFR) allele frequency at 95% confidence interval = 0.872 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	Protein	UniProt
TGFB2	NM_003238.6	c.510+10523T>C		intron_variant		ENST00000366930.9	NP_003229.1
TGFB2	NM_001135599.4	c.594+10523T>C		intron_variant			NP_001129071.1
TGFB2	NR_138148.2	n.1876+10523T>C		intron_variant, non_coding_transcript_variant
TGFB2	NR_138149.2	n.1960+10523T>C		intron_variant, non_coding_transcript_variant

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Protein	Appris	UniProt
TGFB2	ENST00000366930.9	c.510+10523T>C		intron_variant		1	NM_003238.6	ENSP00000355897	P1
TGFB2	ENST00000366929.4	c.594+10523T>C		intron_variant		1		ENSP00000355896
TGFB2	ENST00000488793.1	n.174+10523T>C		intron_variant, non_coding_transcript_variant		3

Frequencies

GnomAD3 genomes AF: 0.586 AC: 88817 AN: 151550 Hom.: 28947 Cov.: 30

Gnomad AFR AF: 0.880

Gnomad AMI AF: 0.395

Gnomad AMR AF: 0.606

Gnomad ASJ AF: 0.458

Gnomad EAS AF: 0.739

Gnomad SAS AF: 0.600

Gnomad FIN AF: 0.455

Gnomad MID AF: 0.503

Gnomad NFE AF: 0.421

Gnomad OTH AF: 0.563

We have no GnomAD4 exomes data on this position. Probably position not covered by the project.

GnomAD4 genome AF: 0.586 AC: 88938 AN: 151668 Hom.: 29011 Cov.: 30 AF XY: 0.589 AC XY: 43602 AN XY: 74072

Gnomad4 AFR AF: 0.880

Gnomad4 AMR AF: 0.607

Gnomad4 ASJ AF: 0.458

Gnomad4 EAS AF: 0.739

Gnomad4 SAS AF: 0.599

Gnomad4 FIN AF: 0.455

Gnomad4 NFE AF: 0.421

Gnomad4 OTH AF: 0.564

Alfa AF: 0.474 Hom.: 11036

Bravo AF: 0.611

Asia WGS AF: 0.644 AC: 2241 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.91
CADD	Benign	0.16
DANN	Benign	0.37

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

LitVar

Other links and lift over

dbSNP: rs2796813; hg19: chr1-218589197;