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NM_014363.6(SACS):c.11326A>G (p.Ile3776Val) AND Spastic paraplegia

Germline classification:
Uncertain significance (1 submission)
Last evaluated:
Aug 17, 2023
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:
RCV002545258.3

Allele description [Variation Report for NM_014363.6(SACS):c.11326A>G (p.Ile3776Val)]

NM_014363.6(SACS):c.11326A>G (p.Ile3776Val)

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.11326A>G (p.Ile3776Val)
HGVS:
  • NC_000013.11:g.23332550T>C
  • NG_012342.1:g.106153A>G
  • NM_001278055.2:c.10885A>G
  • NM_014363.6:c.11326A>GMANE SELECT
  • NP_001264984.1:p.Ile3629Val
  • NP_055178.3:p.Ile3776Val
  • NC_000013.10:g.23906689T>C
  • NM_014363.5:c.11326A>G
Protein change:
I3629V
Links:
dbSNP: rs770269690
NCBI 1000 Genomes Browser:
rs770269690
Molecular consequence:
  • NM_001278055.2:c.10885A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_014363.6:c.11326A>G - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Name:
Spastic paraplegia
Identifiers:
MedGen: C0037772; Human Phenotype Ontology: HP:0001258

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Assertion and evidence details

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Submission AccessionSubmitterReview Status
(Assertion method)		Clinical Significance
(Last evaluated)		OriginMethodCitations
SCV003452233Labcorp Genetics (formerly Invitae), Labcorp
criteria provided, single submitter

(Invitae Variant Classification Sherloc (09022015))		Uncertain significance
(Aug 17, 2023) 		germlineclinical testing

PubMed (1)
[See all records that cite this PMID]

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Summary from all submissions

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

Citations

PubMed

Nothing to display

Details of each submission

From Labcorp Genetics (formerly Invitae), Labcorp, SCV003452233.2

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not providednot providednot providednot providedclinical testing PubMed (1)

Description

In summary, the available evidence is currently insufficient to determine the role of this variant in disease. Therefore, it has been classified as a Variant of Uncertain Significance. Advanced modeling of protein sequence and biophysical properties (such as structural, functional, and spatial information, amino acid conservation, physicochemical variation, residue mobility, and thermodynamic stability) performed at Invitae indicates that this missense variant is not expected to disrupt SACS protein function. ClinVar contains an entry for this variant (Variation ID: 1343970). This variant has not been reported in the literature in individuals affected with SACS-related conditions. This variant is present in population databases (rs770269690, gnomAD 0.0009%). This sequence change replaces isoleucine, which is neutral and non-polar, with valine, which is neutral and non-polar, at codon 3776 of the SACS protein (p.Ile3776Val).

#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1germlineunknownnot providednot providednot providednot providednot providednot providednot provided

Last Updated: Sep 29, 2024