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NM_000546.6(TP53):c.654_672+2dup AND Li-Fraumeni syndrome

Germline classification:
Uncertain significance (1 submission)
Last evaluated:
Jan 16, 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:
RCV001214910.5

Allele description [Variation Report for NM_000546.6(TP53):c.654_672+2dup]

NM_000546.6(TP53):c.654_672+2dup

Gene:
TP53:tumor protein p53 [Gene - OMIM - HGNC]
Variant type:
Duplication
Cytogenetic location:
17p13.1
Genomic location:
Preferred name:
NM_000546.6(TP53):c.654_672+2dup
HGVS:
  • NC_000017.11:g.7674857_7674877dup
  • NC_000017.11:g.7674860_7674880dup
  • NG_017013.2:g.17674_17694dup
  • NM_000546.6:c.654_672+2dupMANE SELECT
  • NM_001126112.3:c.654_672+2dup
  • NM_001126113.3:c.654_672+2dup
  • NM_001126114.3:c.654_672+2dup
  • NM_001126115.2:c.258_276+2dup
  • NM_001126116.2:c.258_276+2dup
  • NM_001126117.2:c.258_276+2dup
  • NM_001126118.2:c.537_555+2dup
  • NM_001276695.3:c.537_555+2dup
  • NM_001276696.3:c.537_555+2dup
  • NM_001276697.3:c.177_195+2dup
  • NM_001276698.3:c.177_195+2dup
  • NM_001276699.3:c.177_195+2dup
  • NM_001276760.3:c.537_555+2dup
  • NM_001276761.3:c.537_555+2dup
  • LRG_321t1:c.654_672+2dup
  • LRG_321:g.17674_17694dup
  • NC_000017.10:g.7578174_7578175insACCTCAGGCGGCTCATAGGGC
  • NC_000017.10:g.7578178_7578198dup
  • NM_000546.5:c.654_672+2dup
Links:
dbSNP: rs2073319024
NCBI 1000 Genomes Browser:
rs2073319024
Molecular consequence:
  • NM_000546.6:c.654_672+2dup - splice donor variant - [Sequence Ontology: SO:0001575]
  • NM_001126112.3:c.654_672+2dup - splice donor variant - [Sequence Ontology: SO:0001575]
  • NM_001126113.3:c.654_672+2dup - splice donor variant - [Sequence Ontology: SO:0001575]
  • NM_001126114.3:c.654_672+2dup - splice donor variant - [Sequence Ontology: SO:0001575]
  • NM_001126115.2:c.258_276+2dup - splice donor variant - [Sequence Ontology: SO:0001575]
  • NM_001126116.2:c.258_276+2dup - splice donor variant - [Sequence Ontology: SO:0001575]
  • NM_001126117.2:c.258_276+2dup - splice donor variant - [Sequence Ontology: SO:0001575]
  • NM_001126118.2:c.537_555+2dup - splice donor variant - [Sequence Ontology: SO:0001575]
  • NM_001276695.3:c.537_555+2dup - splice donor variant - [Sequence Ontology: SO:0001575]
  • NM_001276696.3:c.537_555+2dup - splice donor variant - [Sequence Ontology: SO:0001575]
  • NM_001276697.3:c.177_195+2dup - splice donor variant - [Sequence Ontology: SO:0001575]
  • NM_001276698.3:c.177_195+2dup - splice donor variant - [Sequence Ontology: SO:0001575]
  • NM_001276699.3:c.177_195+2dup - splice donor variant - [Sequence Ontology: SO:0001575]
  • NM_001276760.3:c.537_555+2dup - splice donor variant - [Sequence Ontology: SO:0001575]
  • NM_001276761.3:c.537_555+2dup - splice donor variant - [Sequence Ontology: SO:0001575]

Condition(s)

Name:
Li-Fraumeni syndrome (LFS)
Synonyms:
Sarcoma family syndrome of Li and Fraumeni
Identifiers:
MONDO: MONDO:0018875; MedGen: C0085390; OMIM: PS151623

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Assertion and evidence details

Help
Submission AccessionSubmitterReview Status
(Assertion method)		Clinical Significance
(Last evaluated)		OriginMethodCitations
SCV001386618Invitae
criteria provided, single submitter

(Invitae Variant Classification Sherloc (09022015))		Uncertain significance
(Jan 16, 2023) 		germlineclinical testing

PubMed (3)
[See all records that cite these PMIDs]

Help

Summary from all submissions

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

Citations

PubMed

Aberrant 5' splice sites in human disease genes: mutation pattern, nucleotide structure and comparison of computational tools that predict their utilization.

Buratti E, Chivers M, Královicová J, Romano M, Baralle M, Krainer AR, Vorechovsky I.

Nucleic Acids Res. 2007;35(13):4250-63. Epub 2007 Jun 18.

PubMed [citation]
PMID:
17576681
PMCID:
PMC1934990

Statistical features of human exons and their flanking regions.

Zhang MQ.

Hum Mol Genet. 1998 May;7(5):919-32.

PubMed [citation]
PMID:
9536098
See all PubMed Citations (3)

Details of each submission

From Invitae, SCV001386618.5

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not providednot providednot providednot providedclinical testing PubMed (3)

Description

In summary, the available evidence is currently insufficient to determine the role of this variant in disease. Therefore, it has been classified as a Variant of Uncertain Significance. Variants that disrupt the consensus splice site are a relatively common cause of aberrant splicing (PMID: 17576681, 9536098). RNA analysis performed to evaluate the impact of this variant on mRNA splicing indicates it does not significantly alter splicing (Invitae). ClinVar contains an entry for this variant (Variation ID: 944498). This variant has not been reported in the literature in individuals affected with TP53-related conditions. This variant is not present in population databases (gnomAD no frequency). This sequence change falls in intron 6 of the TP53 gene. It does not directly change the encoded amino acid sequence of the TP53 protein. It affects a nucleotide within the consensus splice site.

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

Last Updated: Feb 28, 2024