chr17-7670637-C-T

Variant names:

• chr17-7670637-C-T
• rs587782237
• NM_000546.6:c.1072G>A

Variant summary

Our verdict is Uncertain significance. The variant received 2 ACMG points: 4P and 2B. PM1 PM2 BP4 BP6

The NM_000546.6(TP53):​c.1072G>A​(p.Glu358Lys) variant causes a missense change. The variant was absent in control chromosomes in GnomAD project. In-silico tool predicts a benign outcome for this variant. Variant has been reported in ClinVar as Conflicting classifications of pathogenicity (no stars). Another variant affecting the same amino acid position, but resulting in a different missense (i.e. E358V) has been classified as Likely benign.

• Frequency: Genomes: not found (cov: 32)
• Consequence: TP53 NM_000546.6 missense
• Clinical Significance: Conflicting classifications of pathogenicity criteria provided, conflicting classifications U:3 B:1
• Conservation: PhyloP100: 3.84
• Publications: 36 publications found

Genes affected

TP53 (HGNC:11998): (tumor protein p53) This gene encodes a tumor suppressor protein containing transcriptional activation, DNA binding, and oligomerization domains. The encoded protein responds to diverse cellular stresses to regulate expression of target genes, thereby inducing cell cycle arrest, apoptosis, senescence, DNA repair, or changes in metabolism. Mutations in this gene are associated with a variety of human cancers, including hereditary cancers such as Li-Fraumeni syndrome. Alternative splicing of this gene and the use of alternate promoters result in multiple transcript variants and isoforms. Additional isoforms have also been shown to result from the use of alternate translation initiation codons from identical transcript variants (PMIDs: 12032546, 20937277). [provided by RefSeq, Dec 2016]

TP53 Gene-Disease associations (from GenCC):

• breast cancer

  Inheritance: AD Classification: DEFINITIVE Submitted by: Ambry Genetics
• Li-Fraumeni syndrome

  Inheritance: AD Classification: DEFINITIVE, STRONG, SUPPORTIVE Submitted by: Labcorp Genetics (formerly Invitae), G2P, ClinGen, Orphanet
• Li-Fraumeni syndrome 1

  Inheritance: AD Classification: DEFINITIVE, STRONG Submitted by: Ambry Genetics, Genomics England PanelApp
• adrenocortical carcinoma, hereditary

  Inheritance: AD Classification: STRONG Submitted by: Ambry Genetics
• sarcoma

  Inheritance: AD Classification: STRONG Submitted by: Genomics England PanelApp
• bone marrow failure syndrome 5

  Inheritance: AD Classification: MODERATE Submitted by: Ambry Genetics
• colorectal cancer

  Inheritance: AD Classification: MODERATE Submitted by: Ambry Genetics
• choroid plexus carcinoma

  Inheritance: AD Classification: SUPPORTIVE Submitted by: Orphanet

ACMG classification

Our verdict: Uncertain_significance. The variant received 2 ACMG points.

• PM1: In a region_of_interest Interaction with HIPK1 (size 270) in uniprot entity P53_HUMAN there are 443 pathogenic changes around while only 181 benign (71%) in NM_000546.6
• PM2: Very rare variant in population databases, with high coverage
• BP4: Computational evidence support a benign effect (MetaRNN=0.28105938).
• BP6: Variant 17-7670637-C-T is Benign according to our data. Variant chr17-7670637-C-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 142105. Variant chr17-7670637-C-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 142105. Variant chr17-7670637-C-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 142105. Variant chr17-7670637-C-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 142105. Variant chr17-7670637-C-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 142105. Variant chr17-7670637-C-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 142105. Variant chr17-7670637-C-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 142105. Variant chr17-7670637-C-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 142105. Variant chr17-7670637-C-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 142105. Variant chr17-7670637-C-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 142105. Variant chr17-7670637-C-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 142105. Variant chr17-7670637-C-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 142105. Variant chr17-7670637-C-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 142105. Variant chr17-7670637-C-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 142105. Variant chr17-7670637-C-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 142105. Variant chr17-7670637-C-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 142105. Variant chr17-7670637-C-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 142105. Variant chr17-7670637-C-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 142105. Variant chr17-7670637-C-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 142105. Variant chr17-7670637-C-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 142105. Variant chr17-7670637-C-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 142105. Variant chr17-7670637-C-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 142105. Variant chr17-7670637-C-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 142105. Variant chr17-7670637-C-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 142105. Variant chr17-7670637-C-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 142105. Variant chr17-7670637-C-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 142105. Variant chr17-7670637-C-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 142105. Variant chr17-7670637-C-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 142105. Variant chr17-7670637-C-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 142105. Variant chr17-7670637-C-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 142105. Variant chr17-7670637-C-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 142105. Variant chr17-7670637-C-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 142105. Variant chr17-7670637-C-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 142105. Variant chr17-7670637-C-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 142105. Variant chr17-7670637-C-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 142105. Variant chr17-7670637-C-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 142105. Variant chr17-7670637-C-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 142105. Variant chr17-7670637-C-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 142105. Variant chr17-7670637-C-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 142105. Variant chr17-7670637-C-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 142105.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
TP53	NM_000546.6	c.1072G>A	p.Glu358Lys	missense_variant	Exon 10 of 11	ENST00000269305.9	NP_000537.3

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
TP53	ENST00000269305.9	c.1072G>A	p.Glu358Lys	missense_variant	Exon 10 of 11	1	NM_000546.6	ENSP00000269305.4

Frequencies

GnomAD3 genomes Cov.: 32

GnomAD4 exome Cov.: 31

GnomAD4 genome Cov.: 32

ClinVar

Significance: Conflicting classifications of pathogenicity

Submissions summary: Uncertain:3 Benign:1

Revision: criteria provided, conflicting classifications

Submissions by phenotype

Hereditary cancer-predisposing syndrome Uncertain:1 Benign:1

Jun 08, 2021

Ambry Genetics

Significance: Likely benign

Review Status: criteria provided, single submitter

Collection Method: clinical testing

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. -

Jun 18, 2022

Genome-Nilou Lab

Significance: Uncertain significance

Review Status: criteria provided, single submitter

Collection Method: clinical testing

- -

Li-Fraumeni syndrome Uncertain:1

Sep 23, 2019

Labcorp Genetics (formerly Invitae), Labcorp

Significance: Uncertain significance

Review Status: criteria provided, single submitter

Collection Method: clinical testing

This variant has been reported not to substantially affect TP53 protein function (PMID: 12826609, 15580553). This sequence change replaces glutamic acid with lysine at codon 358 of the TP53 protein (p.Glu358Lys). The glutamic acid residue is moderately conserved and there is a small physicochemical difference between glutamic acid and lysine. This variant is not present in population databases (ExAC no frequency). This variant has not been reported in the literature in individuals with TP53-related conditions. ClinVar contains an entry for this variant (Variation ID: 142105). 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. -

Li-Fraumeni syndrome 1 Uncertain:1

Jun 18, 2022

Genome-Nilou Lab

Significance: Uncertain significance

Review Status: criteria provided, single submitter

Collection Method: clinical testing

- -

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
AlphaMissense	Benign	0.12
BayesDel_addAF	Uncertain	0.098	D
BayesDel_noAF	Benign	-0.10
CADD	Uncertain	24
DANN	Uncertain	1.0
DEOGEN2	Uncertain	0.66	.;.;.;D;.;D;.;.
Eigen	Benign	-0.099
Eigen_PC	Benign	0.032
FATHMM_MKL	Uncertain	0.95	D
LIST_S2	Uncertain	0.94	D;D;.;.;.;D;D;D
M_CAP	Uncertain	0.095	D
MetaRNN	Benign	0.28	T;T;T;T;T;T;T;T
MetaSVM	Uncertain	0.14	D
MutationAssessor	Benign	1.9	.;.;.;L;.;L;.;.
PhyloP100		3.8
PrimateAI	Benign	0.36	T
PROVEAN	Benign	-0.070	.;.;.;N;.;N;.;.
REVEL	Uncertain	0.30
Sift	Benign	0.10	.;.;.;T;.;T;.;.
Sift4G	Benign	0.48	T;T;T;T;T;T;T;T
Polyphen		0.0080	.;.;.;B;.;B;.;.
Vest4		0.45
MutPred		0.37		.;.;.;Gain of MoRF binding (P = 0.0064);.;Gain of MoRF binding (P = 0.0064);.;.;
MVP		0.84
MPC		0.29
ClinPred		0.67	D
GERP RS		5.4
RBP_binding_hub_radar		0.97
RBP_regulation_power_radar		2.9
Varity_R		0.18
gMVP		0.31

Splicing

Name	Calibrated prediction	Score	Prediction
SpliceAI score (max)		0.0		Details are displayed if max score is > 0.2

Find out detailed SpliceAI scores and Pangolin per-transcript scores at spliceailookup.broadinstitute.org

Other links and lift over

dbSNP: rs587782237; hg19: chr17-7573955; COSMIC: COSV53432060;