chr17:7675070:C>A Detail (hg38) (TP53)

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

Information

Genome

Assembly	Position
hg19	chr17:7,578,388-7,578,388 View the variant detail on this assembly version.
hg38	chr17:7,675,070-7,675,070

HGVS

TP53

Type	Transcript	Protein
RefSeq	NM_000546.5:c.542G>T	NP_000537.3:p.Arg181Leu
	NM_001126112.2:c.542G>T	NP_001119584.1:p.Arg181Leu
	NM_001276760.1:c.542G>T	NP_001263689.1:p.Arg181Leu
	NM_001276761.1:c.542G>T	NP_001263690.1:p.Arg181Leu
	NM_001126113.2:c.542G>T	NP_001119585.1:p.Arg181Leu
	NM_001276695.1:c.542G>T	NP_001263624.1:p.Arg181Leu
	NM_001126116.1:c.146G>T	NP_001119588.1:p.Arg49Leu
	NM_001276698.1:c.146G>T	NP_001263627.1:p.Arg49Leu
	NM_001126118.1:c.425G>T	NP_001119590.1:p.Arg142Leu
	NM_001126117.1:c.65G>T	NP_001119589.1:p.Arg22Leu
	NM_001276699.1:c.65G>T	NP_001263628.1:p.Arg22Leu
	NM_001126115.1:c.65G>T	NP_001119587.1:p.Arg22Leu
	NM_001276697.1:c.65G>T	NP_001263626.1:p.Arg22Leu
	NM_001276696.1:c.425G>T	NP_001263625.1:p.Arg142Leu
Ensemble	ENST00000269305.9:c.542G>T	ENST00000269305.9:p.Arg181Leu
	ENST00000359597.8:c.542G>T	ENST00000359597.8:p.Arg181Leu
	ENST00000413465.6:c.542G>T	ENST00000413465.6:p.Arg181Leu
	ENST00000420246.6:c.542G>T	ENST00000420246.6:p.Arg181Leu
	ENST00000445888.6:c.542G>T	ENST00000445888.6:p.Arg181Leu
	ENST00000455263.6:c.542G>T	ENST00000455263.6:p.Arg181Leu
	ENST00000504290.5:c.146G>T	ENST00000504290.5:p.Arg49Leu
	ENST00000504937.5:c.146G>T	ENST00000504937.5:p.Arg49Leu
	ENST00000510385.5:c.146G>T	ENST00000510385.5:p.Arg49Leu
	ENST00000576024.2:c.542G>T	ENST00000576024.2:p.Arg181Leu
	ENST00000604348.6:c.521G>T	ENST00000604348.6:p.Arg174Leu
	ENST00000610292.4:c.425G>T	ENST00000610292.4:p.Arg142Leu
	ENST00000610538.4:c.425G>T	ENST00000610538.4:p.Arg142Leu
	ENST00000610623.4:c.65G>T	ENST00000610623.4:p.Arg22Leu
	ENST00000618944.4:c.65G>T	ENST00000618944.4:p.Arg22Leu
	ENST00000619186.4:c.65G>T	ENST00000619186.4:p.Arg22Leu
	ENST00000619485.4:c.425G>T	ENST00000619485.4:p.Arg142Leu
	ENST00000620739.4:c.425G>T	ENST00000620739.4:p.Arg142Leu
	ENST00000622645.4:c.425G>T	ENST00000622645.4:p.Arg142Leu
	ENST00000714356.1:c.425G>T	ENST00000714356.1:p.Arg142Leu
	ENST00000714357.1:c.542G>T	ENST00000714357.1:p.Arg181Leu
	ENST00000714359.1:c.542G>T	ENST00000714359.1:p.Arg181Leu
	ENST00000714408.1:c.542G>T	ENST00000714408.1:p.Arg181Leu
	ENST00000714409.1:c.542G>T	ENST00000714409.1:p.Arg181Leu

Summary

MGeND

Clinical significance
Variant entry
GWAS entry
Disease area statistics	Show details

Frequency

[No Data.]

Prediction

ClinVar

Clinical Significance	Uncertain significance
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	COSM6474269	COSMIC
	MONDO

Disease area statistics

[No Data.]

MGeND

[No Data.]

ClinVar

Clinical significance	Last evaluated	Review status	Condition	Origin	Links
risk factor	1994-03-02	no assertion criteria provided	Glioma susceptibility 1	germline	Detail
Uncertain significance	2023-04-27	criteria provided, multiple submitters, no conflicts	Li-Fraumeni syndrome	germline	Detail

CIViC

[No Data.]

DisGeNET

Score	Disease name	Description	Source	Links
0.122	Neoplastic Syndromes, Hereditary	NA	CLINVAR	Detail
0.369	Li-Fraumeni syndrome	NA	CLINVAR	Detail
0.120	Glioma susceptibility 1	NA	CLINVAR	Detail

Annotation

Annotations

Descrption	Source	Links
NM_000546.6(TP53):c.542G>T (p.Arg181Leu) AND Glioma susceptibility 1	ClinVar	Detail
NM_000546.6(TP53):c.542G>T (p.Arg181Leu) AND Li-Fraumeni syndrome	ClinVar	Detail
NA	DisGeNET	Detail
NA	DisGeNET	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: rs397514495 dbSNP
Genome: hg38
Position: chr17:7,675,070-7,675,070
Variant Type: snv
Reference Allele: C
Alternative Allele: A

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