NM_001242897.1(DEPDC5):c.1474C>T (p.Arg492Ter) AND not provided

Clinical significance:Likely pathogenic (Last evaluated: Aug 31, 2016)

Review status:1 star out of maximum of 4 stars

criteria provided, single submitter

Based on:
1 submission [Details]
Record status:
current
Accession:
RCV000416201.1

Allele description [Variation Report for NM_001242897.1(DEPDC5):c.1474C>T (p.Arg492Ter)]

NM_001242897.1(DEPDC5):c.1474C>T (p.Arg492Ter)

Gene:
DEPDC5:DEP domain containing 5 [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
22q12.3
Genomic location:
Preferred name:
NM_001242897.1(DEPDC5):c.1474C>T (p.Arg492Ter)
HGVS:
  • NC_000022.11:g.31815020C>T
  • NG_034067.1:g.66070C>T
  • NM_001242897.1:c.1474C>T
  • NP_001229826.1:p.Arg492Ter
  • NC_000022.10:g.32211006C>T
Protein change:
R492*
Links:
dbSNP: rs1057519107
NCBI 1000 Genomes Browser:
rs1057519107
Molecular consequence:
  • NM_001242897.1:c.1474C>T - nonsense - [Sequence Ontology: SO:0001587]
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
SCV000493197Praxis fuer Humangenetik Tuebingencriteria provided, single submitter
Likely pathogenic
(Aug 31, 2016)
germlineclinical testing

Citation Link

Summary from all submissions

EthnicityOriginAffectedIndividualsFamiliesChromosomes testedNumber TestedFamily historyMethod
not providedgermlineyes1not providednot providednot providednot providedclinical testing

Details of each submission

From Praxis fuer Humangenetik Tuebingen, SCV000493197.6

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

Last Updated: Mar 30, 2019

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