U.S. flag

An official website of the United States government

NM_000051.4(ATM):c.6572+5G>A AND Hereditary cancer-predisposing syndrome

Germline classification:
Uncertain significance (1 submission)
Last evaluated:
Dec 28, 2023
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:
RCV004513818.1

Allele description [Variation Report for NM_000051.4(ATM):c.6572+5G>A]

NM_000051.4(ATM):c.6572+5G>A

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.6572+5G>A
HGVS:
  • NC_000011.10:g.108321425G>A
  • NG_009830.1:g.103594G>A
  • NG_054724.1:g.153408C>T
  • NM_000051.4:c.6572+5G>AMANE SELECT
  • NM_001330368.2:c.641-12354C>T
  • NM_001351110.2:c.*39-12354C>T
  • NM_001351834.2:c.6572+5G>A
  • LRG_135t1:c.6572+5G>A
  • LRG_135:g.103594G>A
  • NC_000011.9:g.108192152G>A
  • NM_000051.3:c.6572+5G>A
Molecular consequence:
  • NM_000051.4:c.6572+5G>A - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001330368.2:c.641-12354C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001351110.2:c.*39-12354C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001351834.2:c.6572+5G>A - intron variant - [Sequence Ontology: SO:0001627]

Condition(s)

Name:
Hereditary cancer-predisposing syndrome
Synonyms:
Neoplastic Syndromes, Hereditary; Tumor predisposition; Cancer predisposition; See all synonyms [MedGen]
Identifiers:
MONDO: MONDO:0015356; MeSH: D009386; MedGen: C0027672

Recent activity

Clear Turn Off Turn On

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

See more...

Assertion and evidence details

Help
Submission AccessionSubmitterReview Status
(Assertion method)		Clinical Significance
(Last evaluated)		OriginMethodCitations
SCV005019330Ambry Genetics
criteria provided, single submitter

(Ambry Variant Classification Scheme 2023)		Uncertain significance
(Dec 28, 2023) 		germlineclinical testing

Citation Link

Help

Summary from all submissions

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

Details of each submission

From Ambry Genetics, SCV005019330.1

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

Description

The c.6572+5G>A intronic variant results from a G to A substitution 5 nucleotides after coding exon 44 in the ATM gene. This nucleotide position is highly conserved in available vertebrate species. In silico splice site analysis for this alteration is inconclusive. Since supporting evidence is limited at this time, the clinical significance of this alteration remains unclear.

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

Last Updated: Oct 26, 2024