rs797044840

Variant names:

• chr1-1338033-TAGGCAGG-C
• rs797044840
• NM_001330311.2:c.1651_1658delCCTGCCTAinsG

Variant summary

Our verdict is Pathogenic. Variant got 11 ACMG points: 11P and 0B. PVS1_Strong PS1 PM2 PP5

The NM_001330311.2(DVL1):​c.1651_1658delCCTGCCTAinsG​(p.Pro551AlafsTer121) variant causes a frameshift, missense change involving the alteration of a conserved nucleotide. The variant was absent in control chromosomes in GnomAD project. Variant has been reported in ClinVar as Pathogenic (no stars). Another nucleotide change resulting in the same amino acid substitution has been previously reported as Pathogenic in Lovd.

• Frequency: Genomes: not found (cov: 32)
• Consequence: DVL1 NM_001330311.2 frameshift, missense
• Clinical Significance: Pathogenic no assertion criteria provided P:1 O:1
• Conservation: PhyloP100: 9.40

Genes affected

DVL1 (HGNC:3084): (dishevelled segment polarity protein 1) DVL1, the human homolog of the Drosophila dishevelled gene (dsh) encodes a cytoplasmic phosphoprotein that regulates cell proliferation, acting as a transducer molecule for developmental processes, including segmentation and neuroblast specification. DVL1 is a candidate gene for neuroblastomatous transformation. The Schwartz-Jampel syndrome and Charcot-Marie-Tooth disease type 2A have been mapped to the same region as DVL1. The phenotypes of these diseases may be consistent with defects which might be expected from aberrant expression of a DVL gene during development. [provided by RefSeq, Jul 2008]

ACMG classification

Verdict is Pathogenic. Variant got 11 ACMG points.

• PVS1: Loss of function variant, product does not undergo nonsense mediated mRNA decay. Variant is located in the 3'-most 50 bp of the penultimate exon, not predicted to undergo nonsense mediated mRNA decay. There are 4 pathogenic variants in the truncated region.
• PS1: Transcript NM_001330311.2 (DVL1) is affected with MISSENSE_VARIANT having same AA change as one Pathogenic present in Lovd
• PM2: Very rare variant in population databases, with high coverage
• PP5: Variant 1-1338033-TAGGCAGG-C is Pathogenic according to our data. Variant chr1-1338033-TAGGCAGG-C is described in ClinVar as [Pathogenic]. Clinvar id is 208050.Status of the report is no_assertion_criteria_provided, 0 stars.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
DVL1	NM_001330311.2	c.1651_1658delCCTGCCTAinsG	p.Pro551AlafsTer121	frameshift_variant, missense_variant	Exon 14 of 15	ENST00000378888.10	NP_001317240.1

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
DVL1	ENST00000378888.10	c.1651_1658delCCTGCCTAinsG	p.Pro551AlafsTer121	frameshift_variant, missense_variant	Exon 14 of 15	5	NM_001330311.2	ENSP00000368166.5
DVL1	ENST00000378891.9	c.1576_1583delCCTGCCTAinsG	p.Pro526AlafsTer121	frameshift_variant, missense_variant	Exon 14 of 15	1		ENSP00000368169.5
DVL1	ENST00000631679.1	c.682_689delCCTGCCTAinsG	p.Pro228AlafsTer21	frameshift_variant, missense_variant	Exon 7 of 8	5		ENSP00000488181.1
DVL1	ENST00000632445.1	c.580_587delCCTGCCTAinsG	p.Pro194AlafsTer21	frameshift_variant, missense_variant	Exon 4 of 6	5		ENSP00000488888.1

Frequencies

GnomAD3 genomes Cov.: 32

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

GnomAD4 genome Cov.: 32

ClinVar

Significance: Pathogenic

Submissions summary: Pathogenic:1 Other:1

Revision: no assertion criteria provided

Submissions by phenotype

Autosomal dominant Robinow syndrome 2 Pathogenic:1 Other:1

Apr 02, 2015

OMIM

Significance: Pathogenic

Review Status: no assertion criteria provided

Collection Method: literature only

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GeneReviews

Significance: not provided

Review Status: no classification provided

Collection Method: literature only

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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: rs797044840; hg19: chr1-1273413;