NM_015046.7:c.5821_5830delGCAATAGAAA

Variant names:

• chr9-132297005-GTTTCTATTGC-G
• rs797045067
• NM_015046.7:c.5821_5830delGCAATAGAAA

Variant summary

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

The NM_015046.7(SETX):​c.5821_5830delGCAATAGAAA​(p.Ala1941LeufsTer6) variant causes a frameshift change. 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: SETX NM_015046.7 frameshift
• Clinical Significance: Pathogenic/Likely pathogenic criteria provided, multiple submitters, no conflicts P:4
• Conservation: PhyloP100: 6.89
• Publications: 1 publications found

Genes affected

SETX (HGNC:445): (senataxin) This gene encodes a protein named for its homology to the Sen1p protein of fungi which has RNA helicase activity encoded by a domain at the C-terminal end of the protein. The protein encoded by this gene contains a DNA/RNA helicase domain at its C-terminal end which suggests that it may be involved in both DNA and RNA processing. Mutations in this gene have been associated with ataxia-ocular apraxia-2 (AOA2) and an autosomal dominant form of juvenile amyotrophic lateral sclerosis (ALS4). [provided by RefSeq, Jul 2008]

SETX Gene-Disease associations (from GenCC):

• amyotrophic lateral sclerosis type 4

  Inheritance: AD Classification: DEFINITIVE, STRONG, SUPPORTIVE Submitted by: Orphanet, Ambry Genetics, Labcorp Genetics (formerly Invitae)
• distal hereditary motor neuropathy

  Inheritance: AD Classification: DEFINITIVE Submitted by: ClinGen
• spinocerebellar ataxia, autosomal recessive, with axonal neuropathy 2

  Inheritance: AR Classification: DEFINITIVE, STRONG, SUPPORTIVE Submitted by: Orphanet, Ambry Genetics, Labcorp Genetics (formerly Invitae)

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 9-132297005-GTTTCTATTGC-G is Pathogenic according to our data. Variant chr9-132297005-GTTTCTATTGC-G is described in ClinVar as Pathogenic/Likely_pathogenic. ClinVar VariationId is 209188.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars.

Variant Effect in Transcripts

ACMG analysis was done for transcript: NM_015046.7. 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
	SETX	NM_015046.7	MANE Select	c.5821_5830delGCAATAGAAA	p.Ala1941LeufsTer6	frameshift	Exon 14 of 26	NP_055861.3
	SETX	NM_001351528.2		c.5821_5830delGCAATAGAAA	p.Ala1941LeufsTer6	frameshift	Exon 14 of 27	NP_001338457.1	Q7Z333-4
	SETX	NM_001351527.2		c.5821_5830delGCAATAGAAA	p.Ala1941LeufsTer6	frameshift	Exon 14 of 26	NP_001338456.1	Q7Z333-1

Ensembl Transcripts

Sel.	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	SETX	ENST00000224140.6	TSL:1 MANE Select	c.5821_5830delGCAATAGAAA	p.Ala1941LeufsTer6	frameshift	Exon 14 of 26	ENSP00000224140.5	Q7Z333-1
	SETX	ENST00000923216.1		c.5821_5830delGCAATAGAAA	p.Ala1941LeufsTer6	frameshift	Exon 14 of 28	ENSP00000593275.1
	SETX	ENST00000923217.1		c.5821_5830delGCAATAGAAA	p.Ala1941LeufsTer6	frameshift	Exon 14 of 27	ENSP00000593276.1

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

ClinVar submissions

Significance: Pathogenic/Likely pathogenic

Revision: criteria provided, multiple submitters, no conflicts

Pathogenic	VUS	Benign	Condition
3	-	-	Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy 2 (3)
1	-	-	Cerebral palsy (1)

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
PhyloP100		6.9
Mutation Taster		=0/200	disease causing (ClinVar)

Splicing

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

Other links and lift over

dbSNP: rs797045067; hg19: chr9-135172392;