NM_000546.6(TP53):c.993+227A>C AND not provided

Germline classification:: Uncertain significance (2 submissions)
Review status:: (0/4) 0 stars out of maximum of 4 stars
no assertion criteria provided

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:: RCV001796025.5

Allele description [Variation Report for NM_000546.6(TP53):c.993+227A>C]

NM_000546.6(TP53):c.993+227A>C

Gene:

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

Variant type:

single nucleotide variant

Cytogenetic location:

17p13.1

Genomic location:

Preferred name:

NM_000546.6(TP53):c.993+227A>C

Other names:

*210S; *342S; *303S; *183S

HGVS:

NC_000017.11:g.7673308T>G
NG_017013.2:g.19243A>C
NM_000546.6:c.993+227A>CMANE SELECT
NM_001126112.3:c.993+227A>C
NM_001126113.3:c.994-42A>C
NM_001126114.3:c.1025A>C
NM_001126115.2:c.597+227A>C
NM_001126116.2:c.629A>C
NM_001126117.2:c.598-42A>C
NM_001126118.2:c.876+227A>C
NM_001276695.3:c.877-42A>C
NM_001276696.3:c.908A>C
NM_001276697.3:c.516+227A>C
NM_001276698.3:c.548A>C
NM_001276699.3:c.517-42A>C
NM_001276760.3:c.876+227A>C
NM_001276761.3:c.876+227A>C
NP_001119586.1:p.Ter342Ser
NP_001119588.1:p.Ter210Ser
NP_001263625.1:p.Ter303Ser
NP_001263627.1:p.Ter183Ser
LRG_321t1:c.993+227A>C
LRG_321:g.19243A>C
NC_000017.10:g.7576626T>G
NM_000546.5:c.993+227A>C

Links:

dbSNP: rs764562217

NCBI 1000 Genomes Browser:

rs764562217

Molecular consequence:

NM_000546.6:c.993+227A>C - intron variant - [Sequence Ontology: SO:0001627]
NM_001126112.3:c.993+227A>C - intron variant - [Sequence Ontology: SO:0001627]
NM_001126113.3:c.994-42A>C - intron variant - [Sequence Ontology: SO:0001627]
NM_001126115.2:c.597+227A>C - intron variant - [Sequence Ontology: SO:0001627]
NM_001126117.2:c.598-42A>C - intron variant - [Sequence Ontology: SO:0001627]
NM_001126118.2:c.876+227A>C - intron variant - [Sequence Ontology: SO:0001627]
NM_001276695.3:c.877-42A>C - intron variant - [Sequence Ontology: SO:0001627]
NM_001276697.3:c.516+227A>C - intron variant - [Sequence Ontology: SO:0001627]
NM_001276699.3:c.517-42A>C - intron variant - [Sequence Ontology: SO:0001627]
NM_001276760.3:c.876+227A>C - intron variant - [Sequence Ontology: SO:0001627]
NM_001276761.3:c.876+227A>C - intron variant - [Sequence Ontology: SO:0001627]
NM_001126114.3:c.1025A>C - stop lost - [Sequence Ontology: SO:0001578]
NM_001126116.2:c.629A>C - stop lost - [Sequence Ontology: SO:0001578]
NM_001276696.3:c.908A>C - stop lost - [Sequence Ontology: SO:0001578]
NM_001276698.3:c.548A>C - stop lost - [Sequence Ontology: SO:0001578]

Condition(s)

Synonyms:: none provided
Identifiers:: MedGen: C3661900

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV002036683	Laboratory of Diagnostic Genome Analysis, Leiden University Medical Center (LUMC) - VKGL Data-share Consensus See additional submitters Diagnostic Laboratory, Department of Genetics, University Medical Center Groningen	no assertion criteria provided	Uncertain significance	germline	clinical testing
SCV002037409	Joint Genome Diagnostic Labs from Nijmegen and Maastricht, Radboudumc and MUMC+ - VKGL Data-share Consensus See additional submitters Diagnostic Laboratory, Department of Genetics, University Medical Center Groningen	no assertion criteria provided	Uncertain significance	germline	clinical testing

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV002036683

Laboratory of Diagnostic Genome Analysis, Leiden University Medical Center (LUMC) - VKGL Data-share Consensus

See additional submitters

no assertion criteria provided

Uncertain significance

germline

clinical testing

SCV002037409

Joint Genome Diagnostic Labs from Nijmegen and Maastricht, Radboudumc and MUMC+ - VKGL Data-share Consensus

See additional submitters

no assertion criteria provided

Uncertain significance

germline

clinical testing

Help

Summary from all submissions

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

Details of each submission

From Laboratory of Diagnostic Genome Analysis, Leiden University Medical Center (LUMC) - VKGL Data-share Consensus, SCV002036683.1

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

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

From Joint Genome Diagnostic Labs from Nijmegen and Maastricht, Radboudumc and MUMC+ - VKGL Data-share Consensus, SCV002037409.1

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

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

Last Updated: Dec 24, 2023

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