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NM_014363.6(SACS):c.3551C>G (p.Pro1184Arg) AND Charlevoix-Saguenay spastic ataxia

Germline classification:
Uncertain significance (1 submission)
Last evaluated:
Feb 12, 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:
RCV001835319.1

Allele description [Variation Report for NM_014363.6(SACS):c.3551C>G (p.Pro1184Arg)]

NM_014363.6(SACS):c.3551C>G (p.Pro1184Arg)

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.3551C>G (p.Pro1184Arg)
HGVS:
  • NC_000013.11:g.23340325G>C
  • NG_012342.1:g.98378C>G
  • NM_001278055.2:c.3110C>G
  • NM_014363.6:c.3551C>GMANE SELECT
  • NP_001264984.1:p.Pro1037Arg
  • NP_055178.3:p.Pro1184Arg
  • NC_000013.10:g.23914464G>C
  • NC_000013.10:g.23914464G>C
  • NM_014363.5:c.3551C>G
Protein change:
P1037R
Links:
dbSNP: rs374961109
NCBI 1000 Genomes Browser:
rs374961109
Molecular consequence:
  • NM_001278055.2:c.3110C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_014363.6:c.3551C>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
SCV002086692Natera, Inc.
no assertion criteria provided
Uncertain significance
(Feb 12, 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., SCV002086692.1

#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: Feb 20, 2024