chrX-133985356-CCGGCGG-C

Variant names:

• chrX-133985356-CCGGCGG-C
• rs749104500
• NM_004484.4:c.88_93delCCGCCG

Variant summary

Our verdict is Uncertain significance. The variant received 1 ACMG points: 2P and 1B. PM2 BP3

The NM_001164617.2(GPC3):​c.88_93delCCGCCG​(p.Pro30_Pro31del) variant causes a conservative inframe deletion 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 Uncertain significance (★). Synonymous variant affecting the same amino acid position (i.e. P30P) has been classified as Likely benign.

• Frequency: Genomes: not found (cov: 23)
• Consequence: GPC3 NM_001164617.2 conservative_inframe_deletion
• Clinical Significance: Uncertain significance criteria provided, single submitter U:1
• Conservation: PhyloP100: 3.06
• Publications: 0 publications found

Genes affected

GPC3 (HGNC:4451): (glypican 3) Cell surface heparan sulfate proteoglycans are composed of a membrane-associated protein core substituted with a variable number of heparan sulfate chains. Members of the glypican-related integral membrane proteoglycan family (GRIPS) contain a core protein anchored to the cytoplasmic membrane via a glycosyl phosphatidylinositol linkage. These proteins may play a role in the control of cell division and growth regulation. The protein encoded by this gene can bind to and inhibit the dipeptidyl peptidase activity of CD26, and it can induce apoptosis in certain cell types. Deletion mutations in this gene are associated with Simpson-Golabi-Behmel syndrome, also known as Simpson dysmorphia syndrome. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2009]

GPC3 Gene-Disease associations (from GenCC):

• Simpson-Golabi-Behmel syndrome

  Inheritance: XL Classification: DEFINITIVE, SUPPORTIVE Submitted by: Orphanet, ClinGen
• Simpson-Golabi-Behmel syndrome type 1

  Inheritance: XL Classification: DEFINITIVE, STRONG Submitted by: G2P, Labcorp Genetics (formerly Invitae), Ambry Genetics

ACMG classification

Our verdict: Uncertain_significance. The variant received 1 ACMG points.

• PM2: Very rare variant in population databases, with high coverage
• BP3: Nonframeshift variant in repetitive region in NM_001164617.2

Variant Effect in Transcripts

ACMG analysis was done for transcript: NM_001164617.2. You can select a different transcript below to see updated ACMG assignments.

RefSeq Transcripts

Sel.	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	GPC3	NM_004484.4	MANE Select	c.88_93delCCGCCG	p.Pro30_Pro31del	conservative_inframe_deletion	Exon 1 of 8	NP_004475.1
	GPC3	NM_001164617.2		c.88_93delCCGCCG	p.Pro30_Pro31del	conservative_inframe_deletion	Exon 1 of 9	NP_001158089.1
	GPC3	NM_001164618.2		c.88_93delCCGCCG	p.Pro30_Pro31del	conservative_inframe_deletion	Exon 1 of 8	NP_001158090.1

Ensembl Transcripts

Sel.	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	GPC3	ENST00000370818.8	TSL:1 MANE Select	c.88_93delCCGCCG	p.Pro30_Pro31del	conservative_inframe_deletion	Exon 1 of 8	ENSP00000359854.3
	GPC3	ENST00000394299.7	TSL:1	c.88_93delCCGCCG	p.Pro30_Pro31del	conservative_inframe_deletion	Exon 1 of 9	ENSP00000377836.2
	GPC3	ENST00000631057.2	TSL:1	c.88_93delCCGCCG	p.Pro30_Pro31del	conservative_inframe_deletion	Exon 1 of 7	ENSP00000486325.1

Frequencies

GnomAD3 genomes Cov.: 23

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

GnomAD4 genome Cov.: 23

ClinVar

ClinVar submissions as Germline

Significance: Uncertain significance

Revision: criteria provided, single submitter

Pathogenic	VUS	Benign	Condition
-	1	-	Wilms tumor 1 (1)

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
PhyloP100		3.1

Splicing

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

Other links and lift over

dbSNP: rs749104500; hg19: chrX-133119383;