9-127825697-GGCCGA-G

Position:

• chr9-127825697-GGCCGA-G

Variant summary

Our verdict is Pathogenic. Variant got 11 ACMG points: 11P and 0B. PVS1 PM2 PP5

The NM_001114753.3(ENG):​c.682_686delTCGGC​(p.Ser228fs) variant causes a frameshift change involving the alteration of a non-conserved nucleotide. The variant was absent in control chromosomes in GnomAD project. Variant has been reported in ClinVar as Pathogenic (no stars). Variant results in nonsense mediated mRNA decay.

• Frequency: Genomes: not found (cov: 31)
• Consequence: ENG NM_001114753.3 frameshift
• Clinical Significance: Pathogenic no assertion criteria provided P:1
• Conservation: PhyloP100: -0.394

Genes affected

ENG (HGNC:3349): (endoglin) This gene encodes a homodimeric transmembrane protein which is a major glycoprotein of the vascular endothelium. This protein is a component of the transforming growth factor beta receptor complex and it binds to the beta1 and beta3 peptides with high affinity. Mutations in this gene cause hereditary hemorrhagic telangiectasia, also known as Osler-Rendu-Weber syndrome 1, an autosomal dominant multisystemic vascular dysplasia. This gene may also be involved in preeclampsia and several types of cancer. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, May 2013]

ACMG classification

Verdict is Pathogenic. Variant got 11 ACMG points.

• PVS1: Loss of function variant, product undergoes nonsense mediated mRNA decay. LoF is a known mechanism of disease.
• PM2: Very rare variant in population databases, with high coverage
• PP5: Variant 9-127825697-GGCCGA-G is Pathogenic according to our data. Variant chr9-127825697-GGCCGA-G is described in ClinVar as [Pathogenic]. Clinvar id is 426041.Status of the report is no_assertion_criteria_provided, 0 stars.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	Protein	UniProt
ENG	NM_001114753.3	c.682_686delTCGGC	p.Ser228fs	frameshift_variant	5/15	ENST00000373203.9	NP_001108225.1
ENG	NM_000118.4	c.682_686delTCGGC	p.Ser228fs	frameshift_variant	5/14		NP_000109.1
ENG	NM_001278138.2	c.136_140delTCGGC	p.Ser46fs	frameshift_variant	5/15		NP_001265067.1
ENG	NM_001406715.1	c.682_686delTCGGC	p.Ser228fs	frameshift_variant	5/8		NP_001393644.1

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Protein	Appris	UniProt
ENG	ENST00000373203.9	c.682_686delTCGGC	p.Ser228fs	frameshift_variant	5/15	1	NM_001114753.3	ENSP00000362299.4
ENG	ENST00000344849.4	c.682_686delTCGGC	p.Ser228fs	frameshift_variant	5/14	1		ENSP00000341917.3
ENG	ENST00000480266.6	c.136_140delTCGGC	p.Ser46fs	frameshift_variant	5/15	2		ENSP00000479015.1

Frequencies

GnomAD3 genomes Cov.: 31

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

GnomAD4 genome Cov.: 31

ClinVar

Significance: Pathogenic

Submissions summary: Pathogenic:1

Revision: no assertion criteria provided

Submissions by phenotype

Pulmonary arterial hypertension related to hereditary hemorrhagic telangiectasia Pathogenic:1

Pathogenic, no assertion criteria provided

literature only

Rare Disease Genomics Group, St George's University of London

-

- -

Computational scores

Source: dbNSFP v4.3

Splicing

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

Publications

LitVar

Other links and lift over

dbSNP: rs1085307430; hg19: chr9-130587976;