NM_014363.6(SACS):c.10461_10462delinsAA (p.Asn3487_Leu3488delinsLysIle) AND not provided

Clinical significance:Uncertain significance (Last evaluated: Jun 15, 2016)

Review status:1 star out of maximum of 4 stars

criteria provided, single submitter

Based on:
1 submission [Details]
Record status:
current
Accession:
RCV000303594.1

Allele description [Variation Report for NM_014363.6(SACS):c.10461_10462delinsAA (p.Asn3487_Leu3488delinsLysIle)]

NM_014363.6(SACS):c.10461_10462delinsAA (p.Asn3487_Leu3488delinsLysIle)

Gene:
SACS:sacsin molecular chaperone [Gene - OMIM - HGNC]
Variant type:
Indel
Cytogenetic location:
13q12.12
Genomic location:
Preferred name:
NM_014363.6(SACS):c.10461_10462delinsAA (p.Asn3487_Leu3488delinsLysIle)
HGVS:
  • NC_000013.11:g.23333414_23333415delinsTT
  • NG_012342.1:g.105288_105289delinsAA
  • NM_001278055.2:c.10020_10021delinsAA
  • NM_014363.6:c.10461_10462delinsAAMANE SELECT
  • NP_001264984.1:p.Asn3340_Leu3341delinsLysIle
  • NP_055178.3:p.Asn3487_Leu3488delinsLysIle
  • NC_000013.10:g.23907553_23907554delinsTT
Links:
dbSNP: rs886043821
NCBI 1000 Genomes Browser:
rs886043821
Molecular consequence:
  • NM_001278055.2:c.10020_10021delinsAA - missense variant - [Sequence Ontology: SO:0001583]
  • NM_014363.6:c.10461_10462delinsAA - missense variant - [Sequence Ontology: SO:0001583]
Observations:
1

Condition(s)

Identifiers:
MedGen: CN517202

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Assertion and evidence details

Submission AccessionSubmitterReview Status
(Assertion method)
Clinical Significance
(Last evaluated)
OriginMethodCitations
SCV000342206EGL Genetic Diagnostics, Eurofins Clinical Diagnosticscriteria provided, single submitter
Uncertain significance
(Jun 15, 2016)
germlineclinical testing

Citation Link

Summary from all submissions

EthnicityOriginAffectedIndividualsFamiliesChromosomes testedNumber TestedFamily historyMethod
not providedgermlineunknown1not providednot providednot providednot providedclinical testing

Details of each submission

From EGL Genetic Diagnostics, Eurofins Clinical Diagnostics, SCV000342206.4

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not provided1not providednot providedclinical testingnot provided
#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1germlineunknownnot providednot providednot provided1not providednot providednot provided

Last Updated: Oct 30, 2020

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