chr17:7578443:A>C Detail (hg19) (TP53)

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Summary
Information
Links
Disease area statistics
MGeND
ClinVar
CIViC
DisGeNET
Annotation
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Information

Genome

Assembly	Position
hg19	chr17:7,578,443-7,578,443
hg38	chr17:7,675,125-7,675,125 View the variant detail on this assembly version.

HGVS

TP53

Type	Transcript	Protein
RefSeq	NM_001126113.2:c.487T>G	NP_001119585.1:p.Tyr163Asp
	NM_001276695.1:c.487T>G	NP_001263624.1:p.Tyr163Asp
	NM_001126115.1:c.10T>G	NP_001119587.1:p.Tyr4Asp
	NM_001276697.1:c.10T>G	NP_001263626.1:p.Tyr4Asp
	NM_001126117.1:c.10T>G	NP_001119589.1:p.Tyr4Asp
	NM_001276699.1:c.10T>G	NP_001263628.1:p.Tyr4Asp
	NM_001276696.1:c.370T>G	NP_001263625.1:p.Tyr124Asp
	NM_001126118.1:c.370T>G	NP_001119590.1:p.Tyr124Asp
	NM_000546.5:c.487T>G	NP_000537.3:p.Tyr163Asp
	NM_001126112.2:c.487T>G	NP_001119584.1:p.Tyr163Asp
	NM_001276760.1:c.487T>G	NP_001263689.1:p.Tyr163Asp
	NM_001276761.1:c.487T>G	NP_001263690.1:p.Tyr163Asp
	NM_001126116.1:c.91T>G	NP_001119588.1:p.Tyr31Asp
	NM_001276698.1:c.91T>G	NP_001263627.1:p.Tyr31Asp
Ensemble	ENST00000618944.4:c.10T>G	ENST00000618944.4:p.Tyr4Asp
	ENST00000445888.6:c.487T>G	ENST00000445888.6:p.Tyr163Asp
	ENST00000455263.6:c.487T>G	ENST00000455263.6:p.Tyr163Asp
	ENST00000619485.4:c.370T>G	ENST00000619485.4:p.Tyr124Asp
	ENST00000620739.4:c.370T>G	ENST00000620739.4:p.Tyr124Asp
	ENST00000504937.5:c.91T>G	ENST00000504937.5:p.Tyr31Asp
	ENST00000619186.4:c.10T>G	ENST00000619186.4:p.Tyr4Asp
	ENST00000714408.1:c.487T>G	ENST00000714408.1:p.Tyr163Asp
	ENST00000576024.2:c.487T>G	ENST00000576024.2:p.Tyr163Asp
	ENST00000610623.4:c.10T>G	ENST00000610623.4:p.Tyr4Asp
	ENST00000420246.6:c.487T>G	ENST00000420246.6:p.Tyr163Asp
	ENST00000622645.4:c.370T>G	ENST00000622645.4:p.Tyr124Asp
	ENST00000604348.6:c.466T>G	ENST00000604348.6:p.Tyr156Asp
	ENST00000359597.8:c.487T>G	ENST00000359597.8:p.Tyr163Asp
	ENST00000714409.1:c.487T>G	ENST00000714409.1:p.Tyr163Asp
	ENST00000413465.6:c.487T>G	ENST00000413465.6:p.Tyr163Asp
	ENST00000714356.1:c.370T>G	ENST00000714356.1:p.Tyr124Asp
	ENST00000714359.1:c.487T>G	ENST00000714359.1:p.Tyr163Asp
	ENST00000610292.4:c.370T>G	ENST00000610292.4:p.Tyr124Asp
	ENST00000269305.9:c.487T>G	ENST00000269305.9:p.Tyr163Asp
	ENST00000504290.5:c.91T>G	ENST00000504290.5:p.Tyr31Asp
	ENST00000714357.1:c.487T>G	ENST00000714357.1:p.Tyr163Asp
	ENST00000510385.5:c.91T>G	ENST00000510385.5:p.Tyr31Asp
	ENST00000610538.4:c.370T>G	ENST00000610538.4:p.Tyr124Asp

Summary

MGeND

Clinical significance
Variant entry
GWAS entry
Disease area statistics	Show details

Frequency

[No Data.]

Prediction

ClinVar

Clinical Significance	Conflicting classifications of pathogenicity
Review star
Show details

Links

TP53

Type	Database	ID	Link
Gene	MIM	191170	OMIM
	HGNC	11998	HGNC
	Ensembl	ENSG00000141510	Ensembl
	NCBI		NCBI
	Gene Cards		Gene Cards
	OncoKB		OncoKB

Type	Database	ID	Link
Variant	TogoVar
	COSMIC	COSM6148120	COSMIC
	MONDO

Disease area statistics

[No Data.]

MGeND

[No Data.]

ClinVar

Clinical significance	Last evaluated	Review status	Condition	Origin	Links
Likely pathogenic	2019-09-20	criteria provided, single submitter	Hereditary cancer-predisposing syndrome	germline	Detail
Likely pathogenic	2016-05-31	no assertion criteria provided	Small cell lung carcinoma	somatic	Detail
Likely pathogenic	2016-05-31	no assertion criteria provided	uterine carcinosarcoma	somatic	Detail
Likely pathogenic	2016-05-31	no assertion criteria provided	hepatocellular carcinoma	somatic	Detail
Likely pathogenic	2016-05-31	no assertion criteria provided	lung adenocarcinoma	somatic	Detail
Likely pathogenic	2016-05-31	no assertion criteria provided	Malignant melanoma of skin	somatic	Detail
Likely pathogenic	2016-05-31	no assertion criteria provided	Breast neoplasm	somatic	Detail
Likely pathogenic	2016-05-31	no assertion criteria provided	Neoplasm of the large intestine	somatic	Detail
Likely pathogenic	2016-05-31	no assertion criteria provided	Neoplasm of brain	somatic	Detail
Likely pathogenic	2016-05-31	no assertion criteria provided	Squamous cell carcinoma of the head and neck	somatic	Detail
Likely pathogenic	2016-05-31	no assertion criteria provided	Carcinoma of esophagus	somatic	Detail
Likely pathogenic	2016-05-31	no assertion criteria provided		somatic	Detail
Likely pathogenic	2016-05-31	no assertion criteria provided	pancreatic adenocarcinoma	somatic	Detail
Likely pathogenic	2016-05-31	no assertion criteria provided	Squamous cell lung carcinoma	somatic	Detail
Likely pathogenic	2016-05-31	no assertion criteria provided	ovarian serous cystadenocarcinoma	somatic	Detail
Uncertain significance	2021-10-18	criteria provided, single submitter	Li-Fraumeni syndrome	germline	Detail

CIViC

[No Data.]

DisGeNET

Score	Disease name	Description	Source	Pubmed	Links
0.122	Neoplastic Syndromes, Hereditary	NA	CLINVAR		Detail

Annotation

Annotations

Descrption	Source	Links
NM_000546.6(TP53):c.487T>G (p.Tyr163Asp) AND Hereditary cancer-predisposing syndrome	ClinVar	Detail
NM_000546.6(TP53):c.487T>G (p.Tyr163Asp) AND Small cell lung carcinoma	ClinVar	Detail
NM_000546.6(TP53):c.487T>G (p.Tyr163Asp) AND Uterine carcinosarcoma	ClinVar	Detail
NM_000546.6(TP53):c.487T>G (p.Tyr163Asp) AND Hepatocellular carcinoma	ClinVar	Detail
NM_000546.6(TP53):c.487T>G (p.Tyr163Asp) AND Lung adenocarcinoma	ClinVar	Detail
NM_000546.6(TP53):c.487T>G (p.Tyr163Asp) AND Malignant melanoma of skin	ClinVar	Detail
NM_000546.6(TP53):c.487T>G (p.Tyr163Asp) AND Breast neoplasm	ClinVar	Detail
NM_000546.6(TP53):c.487T>G (p.Tyr163Asp) AND Neoplasm of the large intestine	ClinVar	Detail
NM_000546.6(TP53):c.487T>G (p.Tyr163Asp) AND Neoplasm of brain	ClinVar	Detail
NM_000546.6(TP53):c.487T>G (p.Tyr163Asp) AND Squamous cell carcinoma of the head and neck	ClinVar	Detail
NM_000546.6(TP53):c.487T>G (p.Tyr163Asp) AND Carcinoma of esophagus	ClinVar	Detail
NM_000546.6(TP53):c.487T>G (p.Tyr163Asp) AND Brainstem glioma	ClinVar	Detail
NM_000546.6(TP53):c.487T>G (p.Tyr163Asp) AND Pancreatic adenocarcinoma	ClinVar	Detail
NM_000546.6(TP53):c.487T>G (p.Tyr163Asp) AND Squamous cell lung carcinoma	ClinVar	Detail
NM_000546.6(TP53):c.487T>G (p.Tyr163Asp) AND Ovarian serous cystadenocarcinoma	ClinVar	Detail
NM_000546.6(TP53):c.487T>G (p.Tyr163Asp) AND Li-Fraumeni syndrome	ClinVar	Detail
NA	DisGeNET	Detail

Overlapped Transcript Coordinates

Gene	Transcript ID	Exon Number	Chromosome	Start	Stop	Type	Amino Mutation	Transcript Position	Links

Overlapped Transcript

Gene	Transcript ID	Chromosome	Start	Stop	Links

Gene: -
dbSNP: rs786203436 dbSNP
Genome: hg19
Position: chr17:7,578,443-7,578,443
Variant Type: snv
Reference Allele: A
Alternative Allele: C

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