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NM_014363.6(SACS):c.8873A>G (p.Lys2958Arg) AND Charlevoix-Saguenay spastic ataxia

Germline classification:
Benign (1 submission)
Last evaluated:
Sep 16, 2020
Review status:
(0/4) 0 stars out of maximum of 4 stars
no assertion criteria provided
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:
RCV001274927.1

Allele description [Variation Report for NM_014363.6(SACS):c.8873A>G (p.Lys2958Arg)]

NM_014363.6(SACS):c.8873A>G (p.Lys2958Arg)

Gene:
SACS:sacsin molecular chaperone [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
13q12.12
Genomic location:
Preferred name:
NM_014363.6(SACS):c.8873A>G (p.Lys2958Arg)
HGVS:
  • NC_000013.11:g.23335003T>C
  • NG_012342.1:g.103700A>G
  • NM_001278055.2:c.8432A>G
  • NM_014363.6:c.8873A>GMANE SELECT
  • NP_001264984.1:p.Lys2811Arg
  • NP_055178.3:p.Lys2958Arg
  • NC_000013.10:g.23909142T>C
  • NM_014363.4:c.8873A>G
  • NM_014363.5:c.8873A>G
  • Q9NZJ4:p.Lys2958Arg
Protein change:
K2811R
Links:
UniProtKB: Q9NZJ4#VAR_059719; dbSNP: rs11839380
NCBI 1000 Genomes Browser:
rs11839380
Molecular consequence:
  • NM_001278055.2:c.8432A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_014363.6:c.8873A>G - missense variant - [Sequence Ontology: SO:0001583]

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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Assertion and evidence details

Help
Submission AccessionSubmitterReview Status
(Assertion method)		Clinical Significance
(Last evaluated)		OriginMethodCitations
SCV001459487Natera, Inc.
no assertion criteria provided
Benign
(Sep 16, 2020) 		germlineclinical testing

Help

Summary from all submissions

EthnicityOriginAffectedIndividualsFamiliesChromosomes testedNumber TestedFamily historyMethod
not providedgermlineunknownnot providednot providednot providednot providednot providedclinical testing

Details of each submission

From Natera, Inc., SCV001459487.1

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not providednot providednot providednot providedclinical testingnot provided
#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1germlineunknownnot providednot providednot providednot providednot providednot providednot provided

Last Updated: Oct 26, 2024