chr13-23340547-A-AT

Variant names:

Variant summary

Our verdict is Pathogenic. The variant received 18 ACMG points: 18P and 0B. PVS1PM2PP5_Very_Strong

The NM_014363.6(SACS):c.3328dupA(p.Ile1110AsnfsTer2) variant causes a frameshift change. The variant allele was found at a frequency of 0.0000105 in 1,611,642 control chromosomes in the GnomAD database, with no homozygous occurrence. Variant has been reported in ClinVar as Likely pathogenic (★★).

Frequency

Genomes: 𝑓 0.0000066 ( 0 hom., cov: 33)

Exomes 𝑓: 0.000011 ( 0 hom. )

Consequence

SACS
NM_014363.6 frameshift

Scores

Not classified

Clinical Significance

Pathogenic/Likely pathogenic criteria provided, multiple submitters, no conflicts P:5

Conservation

PhyloP100: 5.96

Publications

4 publications found

Variant links:

Genes affected

SACS (HGNC:10519): (sacsin molecular chaperone) This gene encodes the sacsin protein, which includes a UbL domain at the N-terminus, a DnaJ domain, and a HEPN domain at the C-terminus. The gene is highly expressed in the central nervous system, also found in skin, skeletal muscles and at low levels in the pancreas. This gene includes a very large exon spanning more than 12.8 kb. Mutations in this gene result in autosomal recessive spastic ataxia of Charlevoix-Saguenay (ARSACS), a neurodegenerative disorder characterized by early-onset cerebellar ataxia with spasticity and peripheral neuropathy. The authors of a publication on the effects of siRNA-mediated sacsin knockdown concluded that sacsin protects against mutant ataxin-1 and suggest that "the large multi-domain sacsin protein is able to recruit Hsp70 chaperone action and has the potential to regulate the effects of other ataxia proteins" (Parfitt et al., PubMed: 19208651). A pseudogene associated with this gene is located on chromosome 11. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, May 2013]

SACS Gene-Disease associations (from GenCC):

Charlevoix-Saguenay spastic ataxia
Inheritance: AR Classification: DEFINITIVE, STRONG, SUPPORTIVE Submitted by: Orphanet, G2P, Laboratory for Molecular Medicine, Labcorp Genetics (formerly Invitae), Myriad Women’s Health

SACS links:

Genome browser will be placed here

ACMG classification

Classification was made for transcript

Our verdict: Pathogenic. The variant received 18 ACMG points.

PVS1

Loss of function variant, product does not undergo nonsense mediated mRNA decay. Variant is located in the 3'-most exon, not predicted to undergo nonsense mediated mRNA decay. There are 681 pathogenic variants in the truncated region.

PM2

Very rare variant in population databases, with high coverage;

PP5

Variant 13-23340547-A-AT is Pathogenic according to our data. Variant chr13-23340547-A-AT is described in CliVar as Pathogenic/Likely_pathogenic. Clinvar id is 189157.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr13-23340547-A-AT is described in CliVar as Pathogenic/Likely_pathogenic. Clinvar id is 189157.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr13-23340547-A-AT is described in CliVar as Pathogenic/Likely_pathogenic. Clinvar id is 189157.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr13-23340547-A-AT is described in CliVar as Pathogenic/Likely_pathogenic. Clinvar id is 189157.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr13-23340547-A-AT is described in CliVar as Pathogenic/Likely_pathogenic. Clinvar id is 189157.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr13-23340547-A-AT is described in CliVar as Pathogenic/Likely_pathogenic. Clinvar id is 189157.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr13-23340547-A-AT is described in CliVar as Pathogenic/Likely_pathogenic. Clinvar id is 189157.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr13-23340547-A-AT is described in CliVar as Pathogenic/Likely_pathogenic. Clinvar id is 189157.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr13-23340547-A-AT is described in CliVar as Pathogenic/Likely_pathogenic. Clinvar id is 189157.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr13-23340547-A-AT is described in CliVar as Pathogenic/Likely_pathogenic. Clinvar id is 189157.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr13-23340547-A-AT is described in CliVar as Pathogenic/Likely_pathogenic. Clinvar id is 189157.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr13-23340547-A-AT is described in CliVar as Pathogenic/Likely_pathogenic. Clinvar id is 189157.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr13-23340547-A-AT is described in CliVar as Pathogenic/Likely_pathogenic. Clinvar id is 189157.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr13-23340547-A-AT is described in CliVar as Pathogenic/Likely_pathogenic. Clinvar id is 189157.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr13-23340547-A-AT is described in CliVar as Pathogenic/Likely_pathogenic. Clinvar id is 189157.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr13-23340547-A-AT is described in CliVar as Pathogenic/Likely_pathogenic. Clinvar id is 189157.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr13-23340547-A-AT is described in CliVar as Pathogenic/Likely_pathogenic. Clinvar id is 189157.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
SACS	NM_014363.6 link	c.3328dupA	p.Ile1110AsnfsTer2	frameshift_variant	Exon 10 of 10	ENST00000382292.9	NP_055178.3	Q9NZJ4-1

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
SACS	ENST00000382292.9 link	c.3328dupA	p.Ile1110AsnfsTer2	frameshift_variant	Exon 10 of 10	5	NM_014363.6	ENSP00000371729.3		Q9NZJ4-1

Frequencies

GnomAD3 genomes

AF:

0.00000658

AC:

AN:

152006

Hom.:

Cov.:

show subpopulations

Gnomad AFR

AF:

0.00

Gnomad AMI

AF:

0.00

Gnomad AMR

AF:

0.00

Gnomad ASJ

AF:

0.00

Gnomad EAS

AF:

0.00

Gnomad SAS

AF:

0.00

Gnomad FIN

AF:

0.00

Gnomad MID

AF:

0.00

Gnomad NFE

AF:

0.00

Gnomad OTH

AF:

0.000478

GnomAD2 exomes

AF:

0.0000412

AC:

AN:

242972

AF XY:

0.0000381

show subpopulations

Gnomad AFR exome

AF:

0.00

Gnomad AMR exome

AF:

0.00

Gnomad ASJ exome

AF:

0.00

Gnomad EAS exome

AF:

0.0000556

Gnomad FIN exome

AF:

0.0000472

Gnomad NFE exome

AF:

0.0000452

Gnomad OTH exome

AF:

0.00

GnomAD4 exome

AF:

0.0000110

AC:

AN:

1459636

Hom.:

Cov.:

AF XY:

0.0000124

AC XY:

AN XY:

726100

show subpopulations

⚠️ The allele balance in gnomAD version 4 Exomes is significantly skewed from the expected value of 0.5.

African (AFR)

AF:

0.00

AC:

AN:

33328

American (AMR)

AF:

0.0000225

AC:

AN:

44346

Ashkenazi Jewish (ASJ)

AF:

0.00

AC:

AN:

26032

East Asian (EAS)

AF:

0.0000252

AC:

AN:

39688

South Asian (SAS)

AF:

0.0000583

AC:

AN:

85786

European-Finnish (FIN)

AF:

0.0000188

AC:

AN:

53332

Middle Eastern (MID)

AF:

0.00

AC:

AN:

5752

European-Non Finnish (NFE)

AF:

0.00000720

AC:

AN:

1111110

Other (OTH)

AF:

0.00

AC:

AN:

60262

⚠️ The allele balance in gnomAD4 Exomes is highly skewed from 0.5 (p-value = 0.002479), which strongly suggests a high chance of mosaicism in these individuals.

Allele Balance Distribution

Red line indicates average allele balance

Average allele balance: 0.397

Heterozygous variant carriers

0.00

0.20

0.40

0.60

0.80

0.95

Allele balance

Age Distribution

Exome Het

Variant carriers

<30

30-35

35-40

40-45

45-50

50-55

55-60

60-65

65-70

70-75

75-80

>80

Age

GnomAD4 genome

AF:

0.00000658

AC:

AN:

152006

Hom.:

Cov.:

AF XY:

0.0000135

AC XY:

AN XY:

74246

show subpopulations

⚠️ The allele balance in gnomAD version 4 Genomes is significantly skewed from the expected value of 0.5.

African (AFR)

AF:

0.00

AC:

AN:

41396

American (AMR)

AF:

0.00

AC:

AN:

15242

Ashkenazi Jewish (ASJ)

AF:

0.00

AC:

AN:

3472

East Asian (EAS)

AF:

0.00

AC:

AN:

5192

South Asian (SAS)

AF:

0.00

AC:

AN:

4822

European-Finnish (FIN)

AF:

0.00

AC:

AN:

10596

Middle Eastern (MID)

AF:

0.00

AC:

AN:

316

European-Non Finnish (NFE)

AF:

0.00

AC:

AN:

67966

Other (OTH)

AF:

0.000478

AC:

AN:

2092

⚠️ The allele balance in gnomAD version 4 Genomes is significantly skewed from the expected value of 0.5. (p-value = 0.000000), which strongly suggests a high chance of mosaicism in these individuals.

Allele Balance Distribution

Red line indicates average allele balance

Average allele balance: 0.225

Heterozygous variant carriers

0.00

0.20

0.40

0.60

0.80

0.95

Allele balance

Age Distribution

Genome Het

Variant carriers

<30

30-35

35-40

40-45

45-50

50-55

55-60

60-65

65-70

70-75

75-80

>80

Age

Alfa

AF:

0.00

Hom.:

Bravo

AF:

0.00000378

ClinVar

Significance: Pathogenic/Likely pathogenic

Submissions summary: Pathogenic:5

Revision: criteria provided, multiple submitters, no conflicts

LINK: link

Submissions by phenotype

Charlevoix-Saguenay spastic ataxia

Pathogenic:4

Jul 01, 2003

OMIM

Significance:Pathogenic

Review Status:no assertion criteria provided

Collection Method:literature only

- -

Oct 05, 2023

Baylor Genetics

Significance:Pathogenic

Review Status:criteria provided, single submitter

Collection Method:clinical testing

- -

Jan 27, 2015

Counsyl

Significance:Likely pathogenic

Review Status:no assertion criteria provided

Collection Method:literature only

This submission and the accompanying classification are no longer maintained by the submitter. For more information on current observations and classification, please contact variantquestions@myriad.com. -

Mar 28, 2024

Fulgent Genetics, Fulgent Genetics

Significance:Likely pathogenic

Review Status:criteria provided, single submitter

Collection Method:clinical testing

- -

Spastic paraplegia

Pathogenic:1

Feb 03, 2023

Labcorp Genetics (formerly Invitae), Labcorp

Significance:Pathogenic

Review Status:criteria provided, single submitter

Collection Method:clinical testing

This premature translational stop signal has been observed in individual(s) with autosomal recessive cerebellar ataxia (PMID: 12873855). It has also been observed to segregate with disease in related individuals. This variant is also known as 1155insA. ClinVar contains an entry for this variant (Variation ID: 189157). For these reasons, this variant has been classified as Pathogenic. The frequency data for this variant in the population databases is considered unreliable, as metrics indicate poor data quality at this position in the gnomAD database. This sequence change creates a premature translational stop signal (p.Ile1110Asnfs*2) in the SACS gene. While this is not anticipated to result in nonsense mediated decay, it is expected to disrupt the last 3470 amino acid(s) of the SACS protein. -

Computational scores

Source: dbNSFP v4.3

Name

Calibrated prediction

Score

Prediction

PhyloP100

6.0

Mutation Taster

=0/200

disease causing (ClinVar)

(source)

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

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Variant summary

Frequency

Consequence

Scores

Clinical Significance

Conservation

Publications

ACMG classification

Transcripts

RefSeq

Ensembl

Frequencies

Age Distribution

Age Distribution

ClinVar

Submissions by phenotype

Computational scores

Splicing

Publications

Other links and lift over