20-57183536-A-G

Position:

• chr20-57183536-A-G

Variant summary

Our verdict is Benign. Variant got -14 ACMG points: 0P and 14B. BP4_Strong BP6_Moderate BA1

The NM_001719.3(BMP7):​c.958+186T>C variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.0621 in 152,212 control chromosomes in the GnomAD database, including 468 homozygotes. In-silico tool predicts a benign outcome for this variant. Variant has been reported in ClinVar as Benign (★).

• Frequency: Genomes: 𝑓 0.062 (468 hom., cov: 33)
• Consequence: BMP7 NM_001719.3 intron
• Clinical Significance: Benign criteria provided, single submitter B:1
• Conservation: PhyloP100: -0.554

Genes affected

BMP7 (HGNC:1074): (bone morphogenetic protein 7) 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, which plays a role in bone, kidney and brown adipose tissue development. Additionally, this protein induces ectopic bone formation and may promote fracture healing in human patients. [provided by RefSeq, Jul 2016]

ACMG classification

Verdict is Benign. Variant got -14 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.91).
• BP6: Variant 20-57183536-A-G is Benign according to our data. Variant chr20-57183536-A-G is described in ClinVar as [Benign]. Clinvar id is 1224759.Status of the report is criteria_provided_single_submitter, 1 stars.
• BA1: GnomAd4 highest subpopulation (AFR) allele frequency at 95% confidence interval = 0.128 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	UniProt
BMP7	NM_001719.3	c.958+186T>C		intron_variant		ENST00000395863.8

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Appris	UniProt
BMP7	ENST00000395863.8	c.958+186T>C		intron_variant		1	NM_001719.3	P1

Frequencies

GnomAD3 genomes AF: 0.0620 AC: 9427 AN: 152094 Hom.: 466 Cov.: 33

Gnomad AFR AF: 0.131

Gnomad AMI AF: 0.0899

Gnomad AMR AF: 0.0310

Gnomad ASJ AF: 0.0115

Gnomad EAS AF: 0.0283

Gnomad SAS AF: 0.0133

Gnomad FIN AF: 0.0503

Gnomad MID AF: 0.0253

Gnomad NFE AF: 0.0376

Gnomad OTH AF: 0.0483

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

GnomAD4 genome AF: 0.0621 AC: 9449 AN: 152212 Hom.: 468 Cov.: 33 AF XY: 0.0609 AC XY: 4535 AN XY: 74420

Gnomad4 AFR AF: 0.131

Gnomad4 AMR AF: 0.0310

Gnomad4 ASJ AF: 0.0115

Gnomad4 EAS AF: 0.0284

Gnomad4 SAS AF: 0.0127

Gnomad4 FIN AF: 0.0503

Gnomad4 NFE AF: 0.0376

Gnomad4 OTH AF: 0.0502

Alfa AF: 0.0688 Hom.: 68

Bravo AF: 0.0640

Asia WGS AF: 0.0480 AC: 168 AN: 3478

ClinVar

Significance: Benign

Submissions summary: Benign:1

Revision: criteria provided, single submitter

Submissions by phenotype

not provided Benign:1

Benign, criteria provided, single submitter

clinical testing

GeneDx

Aug 03, 2018

- -

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.91
CADD	Benign	1.8
DANN	Benign	0.39

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: rs13433113; hg19: chr20-55758592;