NM_000546.6(TP53):c.891C>T (p.His297=) AND not specified

Germline classification:: Likely benign (2 submissions)
Last evaluated:: Sep 3, 2019
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:: RCV000420610.10

Allele description [Variation Report for NM_000546.6(TP53):c.891C>T (p.His297=)]

NM_000546.6(TP53):c.891C>T (p.His297=)

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.891C>T (p.His297=)

HGVS:

NC_000017.11:g.7673729G>A
NG_017013.2:g.18822C>T
NM_000546.6:c.891C>TMANE SELECT
NM_001126112.3:c.891C>T
NM_001126113.3:c.891C>T
NM_001126114.3:c.891C>T
NM_001126115.2:c.495C>T
NM_001126116.2:c.495C>T
NM_001126117.2:c.495C>T
NM_001126118.2:c.774C>T
NM_001276695.3:c.774C>T
NM_001276696.3:c.774C>T
NM_001276697.3:c.414C>T
NM_001276698.3:c.414C>T
NM_001276699.3:c.414C>T
NM_001276760.3:c.774C>T
NM_001276761.3:c.774C>T
NP_000537.3:p.His297=
NP_000537.3:p.His297=
NP_001119584.1:p.His297=
NP_001119585.1:p.His297=
NP_001119586.1:p.His297=
NP_001119587.1:p.His165=
NP_001119588.1:p.His165=
NP_001119589.1:p.His165=
NP_001119590.1:p.His258=
NP_001263624.1:p.His258=
NP_001263625.1:p.His258=
NP_001263626.1:p.His138=
NP_001263627.1:p.His138=
NP_001263628.1:p.His138=
NP_001263689.1:p.His258=
NP_001263690.1:p.His258=
LRG_321t1:c.891C>T
LRG_321:g.18822C>T
LRG_321p1:p.His297=
NC_000017.10:g.7577047G>A
NM_000546.4:c.891C>T
NM_000546.5:c.891C>T
p.H297H
p.His297His

Links:

dbSNP: rs750578863

NCBI 1000 Genomes Browser:

rs750578863

Molecular consequence:

NM_000546.6:c.891C>T - synonymous variant - [Sequence Ontology: SO:0001819]
NM_001126112.3:c.891C>T - synonymous variant - [Sequence Ontology: SO:0001819]
NM_001126113.3:c.891C>T - synonymous variant - [Sequence Ontology: SO:0001819]
NM_001126114.3:c.891C>T - synonymous variant - [Sequence Ontology: SO:0001819]
NM_001126115.2:c.495C>T - synonymous variant - [Sequence Ontology: SO:0001819]
NM_001126116.2:c.495C>T - synonymous variant - [Sequence Ontology: SO:0001819]
NM_001126117.2:c.495C>T - synonymous variant - [Sequence Ontology: SO:0001819]
NM_001126118.2:c.774C>T - synonymous variant - [Sequence Ontology: SO:0001819]
NM_001276695.3:c.774C>T - synonymous variant - [Sequence Ontology: SO:0001819]
NM_001276696.3:c.774C>T - synonymous variant - [Sequence Ontology: SO:0001819]
NM_001276697.3:c.414C>T - synonymous variant - [Sequence Ontology: SO:0001819]
NM_001276698.3:c.414C>T - synonymous variant - [Sequence Ontology: SO:0001819]
NM_001276699.3:c.414C>T - synonymous variant - [Sequence Ontology: SO:0001819]
NM_001276760.3:c.774C>T - synonymous variant - [Sequence Ontology: SO:0001819]
NM_001276761.3:c.774C>T - synonymous variant - [Sequence Ontology: SO:0001819]

Condition(s)

Synonyms:: AllHighlyPenetrant
Identifiers:: MedGen: CN169374

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV000692064	Mayo Clinic Laboratories, Mayo Clinic	no assertion criteria provided	Likely benign	unknown	clinical testing
SCV000697454	Women's Health and Genetics/Laboratory Corporation of America, LabCorp	criteria provided, single submitter (LabCorp Variant Classification Summary - May 2015)	Likely benign (Sep 3, 2019)	germline	clinical testing	Citation Link

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV000692064

Mayo Clinic Laboratories, Mayo Clinic

no assertion criteria provided

Likely benign

unknown

clinical testing

SCV000697454

Women's Health and Genetics/Laboratory Corporation of America, LabCorp

criteria provided, single submitter

(LabCorp Variant Classification Summary - May 2015)

Likely benign
(Sep 3, 2019)

germline

clinical testing

Citation Link

Help

Summary from all submissions

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

Details of each submission

From Mayo Clinic Laboratories, Mayo Clinic, SCV000692064.1

#	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	unknown	unknown	not provided	not provided	not provided		not provided	not provided	not provided	not provided

From Women's Health and Genetics/Laboratory Corporation of America, LabCorp, SCV000697454.2

#	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	unknown	not provided	not provided	not provided		not provided	not provided	not provided	not provided

Last Updated: Oct 13, 2024

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