11-88335088-GAAAA-GAAA

Variant names:

• chr11-88335088-GA-G
• rs11326739
• NM_001814.6:c.173-7delT

Variant summary

Our verdict is Benign. Variant got -16 ACMG points: 0P and 16B. BP6_Very_Strong BA1

The NM_001814.6(CTSC):​c.173-7delT variant causes a splice region, intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.115 in 1,133,870 control chromosomes in the GnomAD database, including 593 homozygotes. 1/1 splice prediction tools predict no significant impact on normal splicing. Variant has been reported in ClinVar as Benign (★★).

• Frequency:
  • Genomes: 𝑓 0.089 (376 hom., cov: 29)
  • Exomes 𝑓: 0.12 (217 hom.)
• Consequence: CTSC NM_001814.6 splice_region, intron
• Clinical Significance: Benign criteria provided, multiple submitters, no conflicts B:3
• Conservation: PhyloP100: -0.410

Genes affected

CTSC (HGNC:2528): (cathepsin C) This gene encodes a member of the peptidase C1 family and lysosomal cysteine proteinase that appears to be a central coordinator for activation of many serine proteinases in cells of the immune system. Alternative splicing results in multiple transcript variants, at least one of which encodes a preproprotein that is proteolytically processed to generate heavy and light chains that form a disulfide-linked dimer. A portion of the propeptide acts as an intramolecular chaperone for the folding and stabilization of the mature enzyme. This enzyme requires chloride ions for activity and can degrade glucagon. Defects in the encoded protein have been shown to be a cause of Papillon-Lefevre syndrome, an autosomal recessive disorder characterized by palmoplantar keratosis and periodontitis. [provided by RefSeq, Nov 2015]

ACMG classification

Verdict is Benign. Variant got -16 ACMG points.

• BP6: Variant 11-88335088-GA-G is Benign according to our data. Variant chr11-88335088-GA-G is described in ClinVar as [Benign]. Clinvar id is 402573.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr11-88335088-GA-G is described in Lovd as [Benign]. Variant chr11-88335088-GA-G is described in Lovd as [Likely_benign].
• BA1: GnomAd4 highest subpopulation (EAS) allele frequency at 95% confidence interval = 0.132 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
CTSC	NM_001814.6	c.173-7delT		splice_region_variant, intron_variant	Intron 1 of 6	ENST00000227266.10	NP_001805.4
CTSC	NM_001114173.3	c.173-7delT		splice_region_variant, intron_variant	Intron 1 of 3		NP_001107645.1
CTSC	NM_148170.5	c.173-7delT		splice_region_variant, intron_variant	Intron 1 of 3		NP_680475.1

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
CTSC	ENST00000227266.10	c.173-7delT		splice_region_variant, intron_variant	Intron 1 of 6	1	NM_001814.6	ENSP00000227266.4

Frequencies

GnomAD3 genomes AF: 0.0892 AC: 9633 AN: 107956 Hom.: 374 Cov.: 29

Gnomad AFR AF: 0.130

Gnomad AMI AF: 0.0387

Gnomad AMR AF: 0.102

Gnomad ASJ AF: 0.00886

Gnomad EAS AF: 0.141

Gnomad SAS AF: 0.0867

Gnomad FIN AF: 0.123

Gnomad MID AF: 0.0417

Gnomad NFE AF: 0.0589

Gnomad OTH AF: 0.0774

GnomAD4 exome AF: 0.118 AC: 120938 AN: 1025878 Hom.: 217 Cov.: 16 AF XY: 0.116 AC XY: 59814 AN XY: 515860

Gnomad4 AFR exome AF: 0.158

Gnomad4 AMR exome AF: 0.154

Gnomad4 ASJ exome AF: 0.0739

Gnomad4 EAS exome AF: 0.192

Gnomad4 SAS exome AF: 0.117

Gnomad4 FIN exome AF: 0.160

Gnomad4 NFE exome AF: 0.111

Gnomad4 OTH exome AF: 0.119

GnomAD4 genome AF: 0.0894 AC: 9652 AN: 107992 Hom.: 376 Cov.: 29 AF XY: 0.0931 AC XY: 4845 AN XY: 52016

Gnomad4 AFR AF: 0.130

Gnomad4 AMR AF: 0.102

Gnomad4 ASJ AF: 0.00886

Gnomad4 EAS AF: 0.142

Gnomad4 SAS AF: 0.0870

Gnomad4 FIN AF: 0.123

Gnomad4 NFE AF: 0.0589

Gnomad4 OTH AF: 0.0792

ClinVar

Significance: Benign

Submissions summary: Benign:3

Revision: criteria provided, multiple submitters, no conflicts

Submissions by phenotype

not specified Benign:1

Mar 28, 2016

Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine

Significance: Benign

Review Status: criteria provided, single submitter

Collection Method: clinical testing

Variant identified in a genome or exome case(s) and assessed due to predicted null impact of the variant or pathogenic assertions in the literature or databases. Disclaimer: This variant has not undergone full assessment. The following are preliminary notes: Frequency -

Papillon-Lefèvre syndrome;C1855627:Haim-Munk syndrome;C4551681:Periodontitis, aggressive 1 Benign:1

Feb 03, 2025

Labcorp Genetics (formerly Invitae), Labcorp

Significance: Benign

Review Status: criteria provided, single submitter

Collection Method: clinical testing

- -

not provided Benign:1

May 04, 2021

GeneDx

Significance: Benign

Review Status: criteria provided, single submitter

Collection Method: clinical testing

- -

Computational scores

Source: dbNSFP v4.3

Splicing

Name	Calibrated prediction	Score	Prediction
SpliceAI score (max)		0.0		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: rs11326739; hg19: chr11-88068256;