chr5-37180085-TCA-T

Variant names:

• chr5-37180085-TCA-T
• rs962476553
• NM_001384732.1:c.5667_5668delTG

Variant summary

Our verdict is Pathogenic. The variant received 18 ACMG points: 18P and 0B. PVS1 PM2 PP5_Very_Strong

The NM_001384732.1(CPLANE1):​c.5667_5668delTG​(p.Asp1890fs) 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 Likely pathogenic (★★). Variant results in nonsense mediated mRNA decay.

• Frequency: Genomes: not found (cov: 32)
• Consequence: CPLANE1 NM_001384732.1 frameshift
• Clinical Significance: Likely pathogenic criteria provided, multiple submitters, no conflicts P:2
• Conservation: PhyloP100: 0.331
• Publications: 0 publications found

Genes affected

CPLANE1 (HGNC:25801): (ciliogenesis and planar polarity effector complex subunit 1) The protein encoded by this gene has putative coiled-coil domains and may be a transmembrane protein. Defects in this gene are a cause of Joubert syndrome (JBTS). [provided by RefSeq, May 2012]

CPLANE1 Gene-Disease associations (from GenCC):

• Joubert syndrome 17

  Inheritance: AR Classification: DEFINITIVE, STRONG Submitted by: Laboratory for Molecular Medicine, ClinGen, G2P, Illumina, Labcorp Genetics (formerly Invitae)
• orofaciodigital syndrome type 6

  Inheritance: AR Classification: DEFINITIVE, STRONG, SUPPORTIVE Submitted by: Labcorp Genetics (formerly Invitae), Orphanet, G2P
• Joubert syndrome

  Inheritance: AR Classification: SUPPORTIVE Submitted by: Orphanet

ACMG classification

Our verdict: Pathogenic. The variant received 18 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 5-37180085-TCA-T is Pathogenic according to our data. Variant chr5-37180085-TCA-T is described in CliVar as Likely_pathogenic. Clinvar id is 445343.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr5-37180085-TCA-T is described in CliVar as Likely_pathogenic. Clinvar id is 445343.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr5-37180085-TCA-T is described in CliVar as Likely_pathogenic. Clinvar id is 445343.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr5-37180085-TCA-T is described in CliVar as Likely_pathogenic. Clinvar id is 445343.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr5-37180085-TCA-T is described in CliVar as Likely_pathogenic. Clinvar id is 445343.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr5-37180085-TCA-T is described in CliVar as Likely_pathogenic. Clinvar id is 445343.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr5-37180085-TCA-T is described in CliVar as Likely_pathogenic. Clinvar id is 445343.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
CPLANE1	NM_001384732.1	c.5667_5668delTG	p.Asp1890fs	frameshift_variant	Exon 28 of 53	ENST00000651892.2	NP_001371661.1

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
CPLANE1	ENST00000651892.2	c.5667_5668delTG	p.Asp1890fs	frameshift_variant	Exon 28 of 53		NM_001384732.1	ENSP00000498265.2

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

Alfa AF: 0.00 Hom.: 0

Bravo AF: 0.00000378

ClinVar

Significance: Likely pathogenic

Submissions summary: Pathogenic:2

Revision: criteria provided, multiple submitters, no conflicts

Submissions by phenotype

Orofaciodigital syndrome type 6;C3553264:Joubert syndrome 17 Pathogenic:1

May 19, 2022

Fulgent Genetics, Fulgent Genetics

Significance: Likely pathogenic

Review Status: criteria provided, single submitter

Collection Method: clinical testing

- -

not provided Pathogenic:1

Apr 18, 2017

Center for Pediatric Genomic Medicine, Children's Mercy Hospital and Clinics

Significance: Likely pathogenic

Review Status: criteria provided, single submitter

Collection Method: clinical testing

- -

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
PhyloP100		0.33
Mutation Taster		=4/196	disease causing (ClinVar)

Splicing

Name	Calibrated prediction	Score	Prediction
SpliceAI score (max)		0.050		Details are displayed if max score is > 0.2

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

Other links and lift over

dbSNP: rs962476553; hg19: chr5-37180187;