NM_000546.6(TP53):c.91G>A (p.Val31Ile) AND Hereditary cancer-predisposing syndrome

Germline classification:: Likely benign (3 submissions)
Last evaluated:: Nov 25, 2021
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:: RCV000115742.24

Allele description [Variation Report for NM_000546.6(TP53):c.91G>A (p.Val31Ile)]

NM_000546.6(TP53):c.91G>A (p.Val31Ile)

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.91G>A (p.Val31Ile)

Other names:

p.V31I:GTT>ATT

HGVS:

NC_000017.11:g.7676387C>T
NG_017013.2:g.16164G>A
NM_000546.6:c.91G>AMANE SELECT
NM_001126112.3:c.91G>A
NM_001126113.3:c.91G>A
NM_001126114.3:c.91G>A
NM_001126118.2:c.-27G>A
NM_001276695.3:c.-27G>A
NM_001276696.3:c.-27G>A
NM_001276760.3:c.-27G>A
NM_001276761.3:c.-27G>A
NP_000537.3:p.Val31Ile
NP_000537.3:p.Val31Ile
NP_001119584.1:p.Val31Ile
NP_001119585.1:p.Val31Ile
NP_001119586.1:p.Val31Ile
LRG_321t1:c.91G>A
LRG_321:g.16164G>A
LRG_321p1:p.Val31Ile
NC_000017.10:g.7579705C>T
NM_000546.4:c.91G>A
NM_000546.5:c.91G>A
P04637:p.Val31Ile
p.V31I

Protein change:

V31I

Links:

UniProtKB: P04637#VAR_044554; dbSNP: rs201753350

NCBI 1000 Genomes Browser:

rs201753350

Molecular consequence:

NM_001126118.2:c.-27G>A - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
NM_001276695.3:c.-27G>A - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
NM_001276696.3:c.-27G>A - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
NM_001276760.3:c.-27G>A - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
NM_001276761.3:c.-27G>A - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
NM_000546.6:c.91G>A - missense variant - [Sequence Ontology: SO:0001583]
NM_001126112.3:c.91G>A - missense variant - [Sequence Ontology: SO:0001583]
NM_001126113.3:c.91G>A - missense variant - [Sequence Ontology: SO:0001583]
NM_001126114.3:c.91G>A - 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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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV000187523	Ambry Genetics	criteria provided, single submitter (Ambry Variant Classification Scheme 2023)	Likely benign (Sep 22, 2020)	germline	clinical testing	PubMed (11) [See all records that cite these PMIDs] 12826609, 17690113, 24728327, 24896186, 25856671, 26332594, 27374712, 29338689, 30352134, 30840781, 31016814 Citation Link,
SCV000910670	Color Diagnostics, LLC DBA Color Health	criteria provided, single submitter (ACMG Guidelines, 2015)	Likely benign (May 20, 2020)	germline	clinical testing	PubMed (1) [See all records that cite this PMID]
SCV002532723	Sema4, Sema4	criteria provided, single submitter (Sema4 Curation Guidelines)	Likely benign (Nov 25, 2021)	germline	curation	Citation Link

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV000187523

Ambry Genetics

criteria provided, single submitter

(Ambry Variant Classification Scheme 2023)

Likely benign
(Sep 22, 2020)

germline

clinical testing

PubMed (11)
[See all records that cite these PMIDs]

Citation Link,

SCV000910670

Color Diagnostics, LLC DBA Color Health

criteria provided, single submitter

(ACMG Guidelines, 2015)

Likely benign
(May 20, 2020)

germline

clinical testing

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

SCV002532723

Sema4, Sema4

criteria provided, single submitter

(Sema4 Curation Guidelines)

Likely benign
(Nov 25, 2021)

germline

curation

Citation Link

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, curation

Citations

PubMed

Understanding the function-structure and function-mutation relationships of p53 tumor suppressor protein by high-resolution missense mutation analysis.

Kato S, Han SY, Liu W, Otsuka K, Shibata H, Kanamaru R, Ishioka C.

Proc Natl Acad Sci U S A. 2003 Jul 8;100(14):8424-9. Epub 2003 Jun 25.

PubMed [citation]

PMID:: 12826609
PMCID:: PMC166245

Identification and characterization of a novel germ line p53 mutation in familial gastric cancer in the Japanese population.

Yamada H, Shinmura K, Okudela K, Goto M, Suzuki M, Kuriki K, Tsuneyoshi T, Sugimura H.

Carcinogenesis. 2007 Sep;28(9):2013-8. Epub 2007 Aug 8.

PubMed [citation]

PMID:: 17690113

See all PubMed Citations (12)

Details of each submission

From Ambry Genetics, SCV000187523.9

#	Ethnicity	Individuals	Chromosomes Tested	Family History	Method	Citations
1	not provided	not provided	not provided	not provided	clinical testing	PubMed (11)

Description

This alteration is classified as likely benign based on a combination of the following: seen in unaffected individuals, population frequency, intact protein function, lack of segregation with disease, co-occurrence, RNA analysis, in silico models, amino acid conservation, lack of disease association in case-control studies, and/or the mechanism of disease or impacted region is inconsistent with a known cause of pathogenicity.

#	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 Color Diagnostics, LLC DBA Color Health, SCV000910670.2

#	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 Sema4, Sema4, SCV002532723.1

#	Ethnicity	Individuals	Chromosomes Tested	Family History	Method	Citations
1	not provided	not provided	not provided	not provided	curation	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: Nov 10, 2024

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