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NM_000051.4(ATM):c.8071C>T (p.Arg2691Cys) AND not provided

Germline classification:
Uncertain significance (1 submission)
Last evaluated:
Dec 8, 2022
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:
RCV000587628.12

Allele description [Variation Report for NM_000051.4(ATM):c.8071C>T (p.Arg2691Cys)]

NM_000051.4(ATM):c.8071C>T (p.Arg2691Cys)

Genes:
ATM:ATM serine/threonine kinase [Gene - OMIM - HGNC]
C11orf65:chromosome 11 open reading frame 65 [Gene - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
11q22.3
Genomic location:
Preferred name:
NM_000051.4(ATM):c.8071C>T (p.Arg2691Cys)
HGVS:
  • NC_000011.10:g.108335029C>T
  • NG_009830.1:g.117198C>T
  • NG_054724.1:g.139804G>A
  • NM_000051.4:c.8071C>TMANE SELECT
  • NM_001330368.2:c.641-25958G>A
  • NM_001351110.2:c.*38+191G>A
  • NM_001351834.2:c.8071C>T
  • NP_000042.3:p.Arg2691Cys
  • NP_000042.3:p.Arg2691Cys
  • NP_001338763.1:p.Arg2691Cys
  • LRG_135t1:c.8071C>T
  • LRG_135:g.117198C>T
  • LRG_135p1:p.Arg2691Cys
  • NC_000011.9:g.108205756C>T
  • NM_000051.3:c.8071C>T
  • p.R2691C
Protein change:
R2691C
Links:
dbSNP: rs531980488
NCBI 1000 Genomes Browser:
rs531980488
Molecular consequence:
  • NM_001330368.2:c.641-25958G>A - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001351110.2:c.*38+191G>A - intron variant - [Sequence Ontology: SO:0001627]
  • NM_000051.4:c.8071C>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001351834.2:c.8071C>T - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Synonyms:
none provided; RECLASSIFIED - ADRA2C POLYMORPHISM; RECLASSIFIED - ADRB1 POLYMORPHISM
Identifiers:
MedGen: C3661900

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Assertion and evidence details

Help
Submission AccessionSubmitterReview Status
(Assertion method)		Clinical Significance
(Last evaluated)		OriginMethodCitations
SCV000568336GeneDx
criteria provided, single submitter

(GeneDx Variant Classification Process June 2021)		Uncertain significance
(Dec 8, 2022) 		germlineclinical testing

Citation Link

Help

Summary from all submissions

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

Details of each submission

From GeneDx, SCV000568336.7

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

Description

In silico analysis supports that this missense variant has a deleterious effect on protein structure/function; Observed in individuals with a personal history of breast or other cancers, but also identified in unaffected controls (Sommer et al., 2003; Heikkinen et al., 2005; Tavtigian et al., 2009; Guarini et al., 2012; Bodian et al., 2014; Yu et al., 2015; Yurgelun et al., 2017; Estiar and Mehdipour, 2018; Hauke et al., 2018; Xie et al., 2018); This variant is associated with the following publications: (PMID: 25563586, 24728327, 30197789, 29731985, 29134647, 12935922, 23633543, 28580595, 26530882, 19781682, 31871109, 15756685, 28135145, 21993670, 29522266, 29880898, 30311369, 33471991, 32107087, 32068069, 28652578, 20305132, 26689913, 31742824, 35406568, 31248605)

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

Last Updated: Nov 30, 2024