1-218349683-A-G

Position:

• chr1-218349683-A-G

Variant summary

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

The NM_003238.6(TGFB2):​c.346+2636A>G variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.0585 in 152,354 control chromosomes in the GnomAD database, including 347 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 0.059 (347 hom., cov: 33)
• Consequence: TGFB2 NM_003238.6 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 0.770

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=-0.5).
• BA1: GnomAd4 highest subpopulation (EAS) allele frequency at 95% confidence interval = 0.125 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	UniProt
TGFB2	NM_003238.6	c.346+2636A>G		intron_variant		ENST00000366930.9
TGFB2	NM_001135599.4	c.346+2636A>G		intron_variant
TGFB2	NR_138148.2	n.1712+2636A>G		intron_variant, non_coding_transcript_variant
TGFB2	NR_138149.2	n.1712+2636A>G		intron_variant, non_coding_transcript_variant

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Appris	UniProt
TGFB2	ENST00000366930.9	c.346+2636A>G		intron_variant		1	NM_003238.6	P1
TGFB2	ENST00000366929.4	c.346+2636A>G		intron_variant		1
TGFB2	ENST00000488793.1	n.10+2636A>G		intron_variant, non_coding_transcript_variant		3

Frequencies

GnomAD3 genomes AF: 0.0585 AC: 8905 AN: 152236 Hom.: 345 Cov.: 33

Gnomad AFR AF: 0.0135

Gnomad AMI AF: 0.0976

Gnomad AMR AF: 0.0742

Gnomad ASJ AF: 0.0481

Gnomad EAS AF: 0.133

Gnomad SAS AF: 0.0896

Gnomad FIN AF: 0.110

Gnomad MID AF: 0.0443

Gnomad NFE AF: 0.0665

Gnomad OTH AF: 0.0569

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

GnomAD4 genome AF: 0.0585 AC: 8913 AN: 152354 Hom.: 347 Cov.: 33 AF XY: 0.0615 AC XY: 4580 AN XY: 74510

Gnomad4 AFR AF: 0.0134

Gnomad4 AMR AF: 0.0743

Gnomad4 ASJ AF: 0.0481

Gnomad4 EAS AF: 0.133

Gnomad4 SAS AF: 0.0899

Gnomad4 FIN AF: 0.110

Gnomad4 NFE AF: 0.0665

Gnomad4 OTH AF: 0.0587

Alfa AF: 0.0613 Hom.: 289

Bravo AF: 0.0524

Asia WGS AF: 0.119 AC: 414 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.50
CADD	Benign	14
DANN	Benign	0.83

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: rs17047682; hg19: chr1-218523025;