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NM_000051.4(ATM):c.877A>T (p.Lys293Ter) AND Familial cancer of breast

Germline classification:
Pathogenic (1 submission)
Last evaluated:
Jan 11, 2024
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:
RCV004022135.1

Allele description [Variation Report for NM_000051.4(ATM):c.877A>T (p.Lys293Ter)]

NM_000051.4(ATM):c.877A>T (p.Lys293Ter)

Gene:
ATM:ATM serine/threonine kinase [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
11q22.3
Genomic location:
Preferred name:
NM_000051.4(ATM):c.877A>T (p.Lys293Ter)
HGVS:
  • NC_000011.10:g.108245002A>T
  • NG_009830.1:g.27171A>T
  • NM_000051.4:c.877A>TMANE SELECT
  • NM_001351834.2:c.877A>T
  • NP_000042.3:p.Lys293Ter
  • NP_000042.3:p.Lys293Ter
  • NP_001338763.1:p.Lys293Ter
  • LRG_135t1:c.877A>T
  • LRG_135:g.27171A>T
  • LRG_135p1:p.Lys293Ter
  • NC_000011.9:g.108115729A>T
  • NM_000051.3:c.877A>T
Protein change:
K293*
Links:
dbSNP: rs1057516442
NCBI 1000 Genomes Browser:
rs1057516442
Molecular consequence:
  • NM_000051.4:c.877A>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001351834.2:c.877A>T - nonsense - [Sequence Ontology: SO:0001587]

Condition(s)

Name:
Familial cancer of breast
Synonyms:
Breast cancer, familial; Hereditary breast cancer
Identifiers:
MONDO: MONDO:0016419; MedGen: C0346153; OMIM: 114480

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Assertion and evidence details

Submission AccessionSubmitterReview Status
(Assertion method)
Clinical Significance
(Last evaluated)
OriginMethodCitations
SCV004931676Myriad Genetics, Inc.
criteria provided, single submitter

(Myriad Autosomal Dominant, Autosomal Recessive and X-Linked Classification Criteria (2023))
Pathogenic
(Jan 11, 2024)
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 Myriad Genetics, Inc., SCV004931676.1

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

Description

This variant is considered pathogenic. This variant creates a termination codon and is predicted to result in premature protein truncation.

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

Last Updated: Sep 29, 2024