NM_000546.6(TP53):c.74+50_74+55dup AND Hereditary cancer-predisposing syndrome

Germline classification:: Likely benign (2 submissions)
Last evaluated:: Jul 19, 2023
Review status:: 2 stars out of maximum of 4 stars
criteria provided, multiple submitters, no conflicts

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:: RCV001175835.3

Allele description [Variation Report for NM_000546.6(TP53):c.74+50_74+55dup]

NM_000546.6(TP53):c.74+50_74+55dup

Gene:

TP53:tumor protein p53 [Gene - OMIM - HGNC]

Variant type:

Duplication

Cytogenetic location:

17p13.1

Genomic location:

Preferred name:

NM_000546.6(TP53):c.74+50_74+55dup

HGVS:

NC_000017.11:g.7676466_7676471dup
NC_000017.11:g.7676470_7676475dup
NG_017013.2:g.16080_16085dup
NM_000546.6:c.74+50_74+55dupMANE SELECT
NM_001126112.3:c.74+50_74+55dup
NM_001126113.3:c.74+50_74+55dup
NM_001126114.3:c.74+50_74+55dup
NM_001126118.2:c.-111_-106dup
NM_001276695.3:c.-44+50_-44+55dup
NM_001276696.3:c.-44+50_-44+55dup
NM_001276760.3:c.-44+50_-44+55dup
NM_001276761.3:c.-44+50_-44+55dup
LRG_321t1:c.74+50_74+55dup
LRG_321:g.16080_16085dup
NC_000017.10:g.7579788_7579793dup
NM_000546.5:c.74+50_74+55dup
NM_000546.6:c.74+50_74+55dupAGCCCCMANE SELECT

Links:

dbSNP: rs2073512697

NCBI 1000 Genomes Browser:

rs2073512697

Molecular consequence:

NM_001126118.2:c.-111_-106dup - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
NM_000546.6:c.74+50_74+55dup - intron variant - [Sequence Ontology: SO:0001627]
NM_001126112.3:c.74+50_74+55dup - intron variant - [Sequence Ontology: SO:0001627]
NM_001126113.3:c.74+50_74+55dup - intron variant - [Sequence Ontology: SO:0001627]
NM_001126114.3:c.74+50_74+55dup - intron variant - [Sequence Ontology: SO:0001627]
NM_001276695.3:c.-44+50_-44+55dup - intron variant - [Sequence Ontology: SO:0001627]
NM_001276696.3:c.-44+50_-44+55dup - intron variant - [Sequence Ontology: SO:0001627]
NM_001276760.3:c.-44+50_-44+55dup - intron variant - [Sequence Ontology: SO:0001627]
NM_001276761.3:c.-44+50_-44+55dup - 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

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV001339604	Color Diagnostics, LLC DBA Color Health	criteria provided, single submitter (ACMG Guidelines, 2015)	Likely benign (Apr 19, 2016)	germline	clinical testing	PubMed (1) [See all records that cite this PMID]
SCV004014905	Institute for Biomarker Research, Medical Diagnostic Laboratories, L.L.C.	criteria provided, single submitter (ACMG Guidelines, 2015)	Likely benign (Jul 19, 2023)	germline	clinical testing	PubMed (1) [See all records that cite this PMID]

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV001339604

Color Diagnostics, LLC DBA Color Health

criteria provided, single submitter

(ACMG Guidelines, 2015)

Likely benign
(Apr 19, 2016)

germline

clinical testing

PubMed (1)
[See all records that cite this PMID]

SCV004014905

Institute for Biomarker Research, Medical Diagnostic Laboratories, L.L.C.

criteria provided, single submitter

(ACMG Guidelines, 2015)

Likely benign
(Jul 19, 2023)

germline

clinical testing

PubMed (1)
[See all records that cite this PMID]

Help

Summary from all submissions

Ethnicity	Origin	Affected	Individuals	Families	Chromosomes tested	Number Tested	Family history	Method
not provided	germline	unknown	not provided	not provided	not provided	not provided	not provided	clinical testing

Citations

PubMed

Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology.

Richards S, Aziz N, Bale S, Bick D, Das S, Gastier-Foster J, Grody WW, Hegde M, Lyon E, Spector E, Voelkerding K, Rehm HL; ACMG Laboratory Quality Assurance Committee..

Genet Med. 2015 May;17(5):405-24. doi: 10.1038/gim.2015.30. Epub 2015 Mar 5.

PubMed [citation]

PMID:: 25741868
PMCID:: PMC4544753

Details of each submission

From Color Diagnostics, LLC DBA Color Health, SCV001339604.1

#	Ethnicity	Individuals	Chromosomes Tested	Family History	Method	Citations
1	not provided	not provided	not provided	not provided	clinical testing	PubMed (1)

#	Sample				Method		Observation
#	Origin	Affected	Number tested	Tissue	Purpose	Method	Individuals	Allele frequency	Families	Co-occurrences
1	germline	unknown	not provided	not provided	not provided		not provided	not provided	not provided	not provided

From Institute for Biomarker Research, Medical Diagnostic Laboratories, L.L.C., SCV004014905.1

#	Ethnicity	Individuals	Chromosomes Tested	Family History	Method	Citations
1	not provided	not provided	not provided	not provided	clinical testing	PubMed (1)

#	Sample				Method		Observation
#	Origin	Affected	Number tested	Tissue	Purpose	Method	Individuals	Allele frequency	Families	Co-occurrences
1	germline	unknown	not provided	not provided	not provided		not provided	not provided	not provided	not provided

Last Updated: Dec 24, 2023

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