rs1106107

Positions:

• chr4-81032591-G-A
• chr4-81032591-G-T

Variant summary

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

The NM_001201.5(BMP3):​c.316+991G>A variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.679 in 152,176 control chromosomes in the GnomAD database, including 39,676 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 0.68 (39676 hom., cov: 33)
• Consequence: BMP3 NM_001201.5 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 0.220

Genes affected

BMP3 (HGNC:1070): (bone morphogenetic protein 3) 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 each subunit of the disulfide-linked homodimer. This protein suppresses osteoblast differentiation, and negatively regulates bone density, by modulating TGF-beta receptor availability to other ligands. [provided by RefSeq, Jul 2016]

ACMG classification

Verdict is Benign. Variant got -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.85).
• BA1: GnomAd4 highest subpopulation (NFE) allele frequency at 95% confidence interval = 0.845 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	Protein	UniProt
BMP3	NM_001201.5	c.316+991G>A		intron_variant		ENST00000282701.4	NP_001192.4
BMP3	XM_006714291.4	c.316+991G>A		intron_variant			XP_006714354.1

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Protein	Appris	UniProt
BMP3	ENST00000282701.4	c.316+991G>A		intron_variant		1	NM_001201.5	ENSP00000282701	P1

Frequencies

GnomAD3 genomes AF: 0.679 AC: 103316 AN: 152058 Hom.: 39662 Cov.: 33

Gnomad AFR AF: 0.288

Gnomad AMI AF: 0.823

Gnomad AMR AF: 0.776

Gnomad ASJ AF: 0.684

Gnomad EAS AF: 0.810

Gnomad SAS AF: 0.821

Gnomad FIN AF: 0.823

Gnomad MID AF: 0.725

Gnomad NFE AF: 0.851

Gnomad OTH AF: 0.697

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

GnomAD4 genome AF: 0.679 AC: 103343 AN: 152176 Hom.: 39676 Cov.: 33 AF XY: 0.682 AC XY: 50739 AN XY: 74392

Gnomad4 AFR AF: 0.287

Gnomad4 AMR AF: 0.777

Gnomad4 ASJ AF: 0.684

Gnomad4 EAS AF: 0.811

Gnomad4 SAS AF: 0.821

Gnomad4 FIN AF: 0.823

Gnomad4 NFE AF: 0.851

Gnomad4 OTH AF: 0.699

Alfa AF: 0.767 Hom.: 12160

Bravo AF: 0.656

Asia WGS AF: 0.774 AC: 2691 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.85
CADD	Benign	5.5
DANN	Benign	0.38

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: rs1106107; hg19: chr4-81953745;