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NM_000051.4(ATM):c.1640C>T (p.Thr547Ile) AND Hereditary cancer-predisposing syndrome

Germline classification:
Uncertain significance (1 submission)
Last evaluated:
Apr 26, 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:
RCV000166950.4

Allele description [Variation Report for NM_000051.4(ATM):c.1640C>T (p.Thr547Ile)]

NM_000051.4(ATM):c.1640C>T (p.Thr547Ile)

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.1640C>T (p.Thr547Ile)
HGVS:
  • NC_000011.10:g.108251869C>T
  • NG_009830.1:g.34038C>T
  • NM_000051.4:c.1640C>TMANE SELECT
  • NM_001351834.2:c.1640C>T
  • NP_000042.3:p.Thr547Ile
  • NP_000042.3:p.Thr547Ile
  • NP_001338763.1:p.Thr547Ile
  • LRG_135t1:c.1640C>T
  • LRG_135:g.34038C>T
  • LRG_135p1:p.Thr547Ile
  • NC_000011.9:g.108122596C>T
  • NM_000051.3:c.1640C>T
  • p.T547I
Protein change:
T547I
Links:
dbSNP: rs786203572
NCBI 1000 Genomes Browser:
rs786203572
Molecular consequence:
  • NM_000051.4:c.1640C>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001351834.2:c.1640C>T - missense variant - [Sequence Ontology: SO:0001583]

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

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Assertion and evidence details

Submission AccessionSubmitterReview Status
(Assertion method)
Clinical Significance
(Last evaluated)
OriginMethodCitations
SCV000217770Ambry Genetics
criteria provided, single submitter

(Ambry Variant Classification Scheme 2023)
Uncertain significance
(Apr 26, 2022)
germlineclinical testing

Citation Link

Summary from all submissions

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

Details of each submission

From Ambry Genetics, SCV000217770.7

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

Description

The p.T547I variant (also known as c.1640C>T), located in coding exon 10 of the ATM gene, results from a C to T substitution at nucleotide position 1640. The threonine at codon 547 is replaced by isoleucine, an amino acid with similar properties. This amino acid position is not well conserved in available vertebrate species. In addition, this alteration is predicted to be tolerated by in silico analysis. 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: Sep 29, 2024