rs1554810037

Variant names:

• chr9-127824312-GCT-G
• rs1554810037
• NM_001114753.3:c.1124_1125delAG

Variant summary

Our verdict is Pathogenic. Variant got 12 ACMG points: 12P and 0B. PVS1 PM2 PP5_Moderate

The NM_001114753.3(ENG):​c.1124_1125delAG​(p.Glu375AlafsTer20) 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 (★). Variant results in nonsense mediated mRNA decay.

• Frequency: Genomes: not found (cov: 30)
• Consequence: ENG NM_001114753.3 frameshift
• Clinical Significance: Pathogenic criteria provided, single submitter P:1
• Conservation: PhyloP100: 0.744

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 12 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 9-127824312-GCT-G is Pathogenic according to our data. Variant chr9-127824312-GCT-G is described in ClinVar as [Pathogenic]. Clinvar id is 458326.Status of the report is criteria_provided_single_submitter, 1 stars.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
ENG	NM_001114753.3	c.1124_1125delAG	p.Glu375AlafsTer20	frameshift_variant	Exon 8 of 15	ENST00000373203.9	NP_001108225.1
ENG	NM_000118.4	c.1124_1125delAG	p.Glu375AlafsTer20	frameshift_variant	Exon 8 of 14		NP_000109.1
ENG	NM_001278138.2	c.578_579delAG	p.Glu193AlafsTer20	frameshift_variant	Exon 8 of 15		NP_001265067.1
ENG	NM_001406715.1	c.1124_1125delAG	p.Glu375AlafsTer23	frameshift_variant	Exon 8 of 8		NP_001393644.1

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
ENG	ENST00000373203.9	c.1124_1125delAG	p.Glu375AlafsTer20	frameshift_variant	Exon 8 of 15	1	NM_001114753.3	ENSP00000362299.4
ENG	ENST00000344849.4	c.1124_1125delAG	p.Glu375AlafsTer20	frameshift_variant	Exon 8 of 14	1		ENSP00000341917.3
ENG	ENST00000480266.6	c.578_579delAG	p.Glu193AlafsTer20	frameshift_variant	Exon 8 of 15	2		ENSP00000479015.1
ENG	ENST00000486329.1	n.92_93delAG		non_coding_transcript_exon_variant	Exon 1 of 3	2

Frequencies

GnomAD3 genomes Cov.: 30

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

GnomAD4 genome Cov.: 30

ClinVar

Significance: Pathogenic

Submissions summary: Pathogenic:1

Revision: criteria provided, single submitter

Submissions by phenotype

Telangiectasia, hereditary hemorrhagic, type 1 Pathogenic:1

Apr 08, 2017

Labcorp Genetics (formerly Invitae), Labcorp

Significance: Pathogenic

Review Status: criteria provided, single submitter

Collection Method: clinical testing

This sequence change deletes 2 nucleotides from exon 8 of the ENG mRNA (c.1124_1125delAG), causing a frameshift at codon 375. This creates a premature translational stop signal (p.Glu375Alafs*20) and is expected to result in an absent or disrupted protein product. Loss-of-function variants in ENG are known to be pathogenic. This particular variant has been reported in the literature in individuals with hereditary hemorrhagic telangiectasia (PMID: 16752392, 23801935). For these reasons, this variant has been classified as Pathogenic. -

Computational scores

Source: dbNSFP v4.3

Splicing

Name	Calibrated prediction	Score	Prediction
SpliceAI score (max)		0.020		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: rs1554810037; hg19: chr9-130586591;