NM_000051.4(ATM):c.7705_7706del (p.Arg2568_Asp2569insTer) AND not provided

Clinical significance:Pathogenic (Last evaluated: Oct 5, 2021)

Review status:1 star out of maximum of 4 stars

criteria provided, single submitter

Based on:
1 submission [Details]
Record status:
current
Accession:
RCV000478786.3

Allele description [Variation Report for NM_000051.4(ATM):c.7705_7706del (p.Arg2568_Asp2569insTer)]

NM_000051.4(ATM):c.7705_7706del (p.Arg2568_Asp2569insTer)

Genes:
ATM:ATM serine/threonine kinase [Gene - OMIM - HGNC]
C11orf65:chromosome 11 open reading frame 65 [Gene - HGNC]
Variant type:
Microsatellite
Cytogenetic location:
11q22.3
Genomic location:
Preferred name:
NM_000051.4(ATM):c.7705_7706del (p.Arg2568_Asp2569insTer)
HGVS:
  • NC_000011.10:g.108331952GA[1]
  • NG_009830.1:g.114121GA[1]
  • NG_054724.1:g.142879CT[1]
  • NM_000051.4:c.7705_7706delMANE SELECT
  • NM_001330368.2:c.641-22881_641-22880del
  • NM_001351110.2:c.*38+3268_*38+3269del
  • NM_001351834.2:c.7705_7706del
  • NP_000042.3:p.Arg2568_Asp2569insTer
  • NP_001338763.1:p.Arg2568_Asp2569insTer
  • LRG_135t1:c.7705_7706del
  • LRG_135:g.114121GA[1]
  • NC_000011.9:g.108202678_108202679del
  • NC_000011.9:g.108202679GA[1]
  • NM_000051.3:c.7702_7703delAG
  • NM_000051.3:c.7705_7706del
  • NM_000051.3:c.7705_7706delGA
Links:
dbSNP: rs759965045
NCBI 1000 Genomes Browser:
rs759965045
Molecular consequence:
  • NM_001330368.2:c.641-22881_641-22880del - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001351110.2:c.*38+3268_*38+3269del - intron variant - [Sequence Ontology: SO:0001627]
  • NM_000051.4:c.7705_7706del - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001351834.2:c.7705_7706del - nonsense - [Sequence Ontology: SO:0001587]

Condition(s)

Identifiers:
MedGen: CN517202

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Assertion and evidence details

Submission AccessionSubmitterReview Status
(Assertion method)
Clinical Significance
(Last evaluated)
OriginMethodCitations
SCV000565939GeneDxcriteria provided, single submitter
Pathogenic
(Oct 5, 2021)
germlineclinical testing

Citation Link

Summary from all submissions

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

Details of each submission

From GeneDx, SCV000565939.5

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not providednot providednot providednot providedclinical testingnot provided

Description

Not observed at a significant frequency in large population cohorts (Lek 2016); Nonsense variant predicted to result in protein truncation or nonsense mediated decay in a gene for which loss-of-function is a known mechanism of disease; This variant is associated with the following publications: (PMID: 29025585, 10330348, 10817650, 12815592, 30128536, 30262796, 29625052, 26689913)

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

Last Updated: Nov 27, 2021

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