NM_182649.2(PCNA):c.443G>C (p.Cys148Ser) AND Ataxia-telangiectasia-like disorder 2

Clinical significance:Likely pathogenic (Last evaluated: May 28, 2019)

Review status:1 star out of maximum of 4 stars

criteria provided, single submitter

Based on:
1 submission [Details]
Record status:
current
Accession:
RCV000990278.1

Allele description [Variation Report for NM_182649.2(PCNA):c.443G>C (p.Cys148Ser)]

NM_182649.2(PCNA):c.443G>C (p.Cys148Ser)

Gene:
PCNA:proliferating cell nuclear antigen [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
20p12.3
Genomic location:
Preferred name:
NM_182649.2(PCNA):c.443G>C (p.Cys148Ser)
HGVS:
  • NC_000020.11:g.5117609C>G
  • NG_047066.1:g.14014G>C
  • NG_053057.1:g.479G>C
  • NM_002592.2:c.443G>C
  • NM_182649.2:c.443G>CMANE SELECT
  • NP_002583.1:p.Cys148Ser
  • NP_872590.1:p.Cys148Ser
  • NC_000020.10:g.5098255C>G
Protein change:
C148S
Links:
dbSNP: rs1274412848
NCBI 1000 Genomes Browser:
rs1274412848
Molecular consequence:
  • NM_002592.2:c.443G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_182649.2:c.443G>C - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Name:
Ataxia-telangiectasia-like disorder 2 (ATLD2)
Identifiers:
MONDO: MONDO:0014399; MedGen: C4014676; Orphanet: 438134; OMIM: 615919

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Assertion and evidence details

Submission AccessionSubmitterReview Status
(Assertion method)
Clinical Significance
(Last evaluated)
OriginMethodCitations
SCV001141206Mendelicscriteria provided, single submitter
Likely pathogenic
(May 28, 2019)
unknownclinical testing

Citation Link

Summary from all submissions

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

Details of each submission

From Mendelics, SCV001141206.1

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

Last Updated: Jun 27, 2020

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