chr17:7673778:T>C Detail (hg38) (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	chr17:7,577,096-7,577,096 View the variant detail on this assembly version.
hg38	chr17:7,673,778-7,673,778

HGVS

TP53

Type	Transcript	Protein
RefSeq	NM_001126115.1:c.365A>G	NP_001119587.1:p.Asp122Gly
	NM_001276697.1:c.365A>G	NP_001263626.1:p.Asp122Gly
	NM_001276696.1:c.725A>G	NP_001263625.1:p.Asp242Gly
	NM_000546.5:c.842A>G	NP_000537.3:p.Asp281Gly
	NM_001126112.2:c.842A>G	NP_001119584.1:p.Asp281Gly
	NM_001276760.1:c.842A>G	NP_001263689.1:p.Asp281Gly
	NM_001276761.1:c.842A>G	NP_001263690.1:p.Asp281Gly
	NM_001126113.2:c.842A>G	NP_001119585.1:p.Asp281Gly
	NM_001276695.1:c.842A>G	NP_001263624.1:p.Asp281Gly
	NM_001126116.1:c.446A>G	NP_001119588.1:p.Asp149Gly
	NM_001276698.1:c.446A>G	NP_001263627.1:p.Asp149Gly
	NM_001126118.1:c.725A>G	NP_001119590.1:p.Asp242Gly
	NM_001126117.1:c.365A>G	NP_001119589.1:p.Asp122Gly
	NM_001276699.1:c.365A>G	NP_001263628.1:p.Asp122Gly
Ensemble	ENST00000618944.4:c.365A>G	ENST00000618944.4:p.Asp122Gly
	ENST00000619186.4:c.365A>G	ENST00000619186.4:p.Asp122Gly
	ENST00000619485.4:c.725A>G	ENST00000619485.4:p.Asp242Gly
	ENST00000620739.4:c.725A>G	ENST00000620739.4:p.Asp242Gly
	ENST00000622645.4:c.725A>G	ENST00000622645.4:p.Asp242Gly
	ENST00000269305.9:c.842A>G	ENST00000269305.9:p.Asp281Gly
	ENST00000359597.8:c.842A>G	ENST00000359597.8:p.Asp281Gly
	ENST00000413465.6:c.782+403A>G
	ENST00000420246.6:c.842A>G	ENST00000420246.6:p.Asp281Gly
	ENST00000445888.6:c.842A>G	ENST00000445888.6:p.Asp281Gly
	ENST00000455263.6:c.842A>G	ENST00000455263.6:p.Asp281Gly
	ENST00000504290.5:c.446A>G	ENST00000504290.5:p.Asp149Gly
	ENST00000504937.5:c.446A>G	ENST00000504937.5:p.Asp149Gly
	ENST00000510385.5:c.446A>G	ENST00000510385.5:p.Asp149Gly
	ENST00000576024.2:c.842A>G	ENST00000576024.2:p.Asp281Gly
	ENST00000604348.6:c.821A>G	ENST00000604348.6:p.Asp274Gly
	ENST00000610292.4:c.725A>G	ENST00000610292.4:p.Asp242Gly
	ENST00000610538.4:c.725A>G	ENST00000610538.4:p.Asp242Gly
	ENST00000610623.4:c.365A>G	ENST00000610623.4:p.Asp122Gly
	ENST00000714356.1:c.725A>G	ENST00000714356.1:p.Asp242Gly
	ENST00000714357.1:c.842A>G	ENST00000714357.1:p.Asp281Gly
	ENST00000714359.1:c.842A>G	ENST00000714359.1:p.Asp281Gly
	ENST00000714408.1:c.842A>G	ENST00000714408.1:p.Asp281Gly
	ENST00000714409.1:c.842A>G	ENST00000714409.1:p.Asp281Gly

Summary

MGeND

Clinical significance
Variant entry
GWAS entry
Disease area statistics	Show details

Frequency

[No Data.]

Prediction

ClinVar

Clinical Significance	Pathogenic
Review star
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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	COSM4271754	COSMIC
	MONDO

Disease area statistics

[No Data.]

MGeND

[No Data.]

ClinVar

Clinical significance	Last evaluated	Review status	Condition	Origin	Links
Pathogenic	2022-08-11	criteria provided, multiple submitters, no conflicts	Hereditary cancer-predisposing syndrome	germline	Detail
Likely pathogenic	2016-05-31	no assertion criteria provided	gastric adenocarcinoma	somatic	Detail
Likely pathogenic	2016-05-31	no assertion criteria provided	Malignant neoplasm of body of uterus	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	multiple myeloma	somatic	Detail
Likely pathogenic	2016-05-31	no assertion criteria provided	neuroblastoma	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		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	Papillary renal cell carcinoma type 1	somatic	Detail
Likely pathogenic	2016-05-31	no assertion criteria provided	lung adenocarcinoma	somatic	Detail
Likely pathogenic	2016-05-31	no assertion criteria provided	glioblastoma	somatic	Detail
Likely pathogenic	2016-05-31	no assertion criteria provided		somatic	Detail
Likely pathogenic	2016-05-31	no assertion criteria provided	Breast neoplasm	somatic	Detail
Likely pathogenic	2016-05-31	no assertion criteria provided	ovarian serous cystadenocarcinoma	somatic	Detail
Likely pathogenic	2016-05-31	no assertion criteria provided	pancreatic adenocarcinoma	somatic	Detail
Likely pathogenic	2016-05-31	no assertion criteria provided	B-cell chronic lymphocytic leukemia	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
Pathogenic	2024-01-12	criteria provided, multiple submitters, no conflicts	Li-Fraumeni syndrome	germline unknown	Detail
Pathogenic	2022-06-18	criteria provided, multiple submitters, no conflicts	Li-Fraumeni syndrome 1	germline	Detail
Pathogenic	2021-11-03	criteria provided, single submitter	not provided	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.842A>G (p.Asp281Gly) AND Hereditary cancer-predisposing syndrome	ClinVar	Detail
NM_000546.6(TP53):c.842A>G (p.Asp281Gly) AND Gastric adenocarcinoma	ClinVar	Detail
NM_000546.6(TP53):c.842A>G (p.Asp281Gly) AND Malignant neoplasm of body of uterus	ClinVar	Detail
NM_000546.6(TP53):c.842A>G (p.Asp281Gly) AND Squamous cell lung carcinoma	ClinVar	Detail
NM_000546.6(TP53):c.842A>G (p.Asp281Gly) AND Multiple myeloma	ClinVar	Detail
NM_000546.6(TP53):c.842A>G (p.Asp281Gly) AND Neuroblastoma	ClinVar	Detail
NM_000546.6(TP53):c.842A>G (p.Asp281Gly) AND Squamous cell carcinoma of the head and neck	ClinVar	Detail
NM_000546.6(TP53):c.842A>G (p.Asp281Gly) AND Transitional cell carcinoma of the bladder	ClinVar	Detail
NM_000546.6(TP53):c.842A>G (p.Asp281Gly) AND Malignant melanoma of skin	ClinVar	Detail
NM_000546.6(TP53):c.842A>G (p.Asp281Gly) AND Papillary renal cell carcinoma type 1	ClinVar	Detail
NM_000546.6(TP53):c.842A>G (p.Asp281Gly) AND Lung adenocarcinoma	ClinVar	Detail
NM_000546.6(TP53):c.842A>G (p.Asp281Gly) AND Glioblastoma	ClinVar	Detail
NM_000546.6(TP53):c.842A>G (p.Asp281Gly) AND Squamous cell carcinoma of the skin	ClinVar	Detail
NM_000546.6(TP53):c.842A>G (p.Asp281Gly) AND Breast neoplasm	ClinVar	Detail
NM_000546.6(TP53):c.842A>G (p.Asp281Gly) AND Ovarian serous cystadenocarcinoma	ClinVar	Detail
NM_000546.6(TP53):c.842A>G (p.Asp281Gly) AND Pancreatic adenocarcinoma	ClinVar	Detail
NM_000546.6(TP53):c.842A>G (p.Asp281Gly) AND B-cell chronic lymphocytic leukemia	ClinVar	Detail
NM_000546.6(TP53):c.842A>G (p.Asp281Gly) AND Uterine carcinosarcoma	ClinVar	Detail
NM_000546.6(TP53):c.842A>G (p.Asp281Gly) AND Hepatocellular carcinoma	ClinVar	Detail
NM_000546.6(TP53):c.842A>G (p.Asp281Gly) AND Li-Fraumeni syndrome	ClinVar	Detail
NM_000546.6(TP53):c.842A>G (p.Asp281Gly) AND Li-Fraumeni syndrome 1	ClinVar	Detail
NM_000546.6(TP53):c.842A>G (p.Asp281Gly) AND not provided	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: rs587781525 dbSNP
Genome: hg38
Position: chr17:7,673,778-7,673,778
Variant Type: snv
Reference Allele: T
Alternative Allele: C

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