NM_014363.6(SACS):c.468_469insG (p.Tyr157fs) AND Charlevoix-Saguenay spastic ataxia

Germline classification:: Likely pathogenic (1 submission)
Last evaluated:: Apr 28, 2016
Review status:: 1 star out of maximum of 4 stars
criteria provided, single submitter

Somatic classification of clinical impact:: None
Review status:: (0/4) 0 stars out of maximum of 4 stars
no assertion criteria provided

Somatic classification of oncogenicity:: None
Review status:: (0/4) 0 stars out of maximum of 4 stars
no assertion criteria provided

Record status:: current
Accession:: RCV000409711.2

Allele description [Variation Report for NM_014363.6(SACS):c.468_469insG (p.Tyr157fs)]

NM_014363.6(SACS):c.468_469insG (p.Tyr157fs)

Gene:

SACS:sacsin molecular chaperone [Gene - OMIM - HGNC]

Variant type:

Insertion

Cytogenetic location:

13q12.12

Genomic location:

Preferred name:

NM_014363.6(SACS):c.468_469insG (p.Tyr157fs)

HGVS:

NC_000013.11:g.23358470_23358471insC
NG_012342.1:g.80232_80233insG
NM_001278055.2:c.27_28insG
NM_014363.6:c.468_469insGMANE SELECT
NP_001264984.1:p.Tyr10fs
NP_055178.3:p.Tyr157fs
NC_000013.10:g.23932609_23932610insC
NM_014363.4:c.468_469insG

Protein change:

Y10fs

Links:

dbSNP: rs1057516820

NCBI 1000 Genomes Browser:

rs1057516820

Molecular consequence:

NM_001278055.2:c.27_28insG - frameshift variant - [Sequence Ontology: SO:0001589]
NM_014363.6:c.468_469insG - frameshift variant - [Sequence Ontology: SO:0001589]

Condition(s)

Name:: Charlevoix-Saguenay spastic ataxia (SACS)
Synonyms:: Autosomal recessive spastic ataxia of Charlevoix-Saguenay; Spastic ataxia of Charlevoix-Saguenay; SPASTIC ATAXIA 6, AUTOSOMAL RECESSIVE
Identifiers:: MONDO: MONDO:0010041; MedGen: C1849140; Orphanet: 98; OMIM: 270550

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Synthetic construct Homo sapiens clone IMAGE:100069265, MGC:199276 zinc finger p...
Synthetic construct Homo sapiens clone IMAGE:100069265, MGC:199276 zinc finger protein 626 (ZNF626) mRNA, encodes complete protein
gi|225000295|gb|BC172571.1|

Nucleotide

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV000486284	Counsyl	criteria provided, single submitter (Counsyl Autosomal and X-linked Recessive Disease Classification criteria (2015))	Likely pathogenic (Apr 28, 2016)	unknown	clinical testing	mdi-5618_320494_Counsyl Autosomal and X-linked Recessive Disease Classification criteria (2015).pdf Citation Link

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV000486284

Counsyl

criteria provided, single submitter

(Counsyl Autosomal and X-linked Recessive Disease Classification criteria (2015))

Likely pathogenic
(Apr 28, 2016)

unknown

clinical testing

mdi-5618_320494_Counsyl Autosomal and X-linked Recessive Disease Classification criteria (2015).pdf

Citation Link

Help

Summary from all submissions

Ethnicity	Origin	Affected	Individuals	Families	Chromosomes tested	Number Tested	Family history	Method
not provided	unknown	unknown	not provided	not provided	not provided	not provided	not provided	clinical testing

Details of each submission

From Counsyl, SCV000486284.2

#	Ethnicity	Individuals	Chromosomes Tested	Family History	Method	Citations
1	not provided	not provided	not provided	not provided	clinical testing	not provided

#	Sample				Method		Observation
#	Origin	Affected	Number tested	Tissue	Purpose	Method	Individuals	Allele frequency	Families	Co-occurrences
1	unknown	unknown	not provided	not provided	not provided		not provided	not provided	not provided	not provided

Last Updated: Dec 24, 2022

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