Favorite

Mutation Direct

Effortless mutation search and display tool

Search criteria：

Gene: TP53 & Disease: Gliosarcoma, 1798 results

ClinVar	Gene	Nucleotide	Amino Acid	Transcript ID	Mutation type	Clinical Significance	Disease count	Publications
12356	TP53	c.743G>A	p.Arg248Gln (p.R248Q)	NM_000546.6 M	SNV	P	46 +	82
	TP53	c.743G>A	p.Arg248Gln (p.R248Q)	NM_001126112.3	SNV	P	46 +	82
	TP53	c.743G>A	p.Arg248Gln (p.R248Q)	NM_001126113.3	SNV	P	46 +	82
	TP53	c.743G>A	p.Arg248Gln (p.R248Q)	NM_001126114.3	SNV	P	46 +	82
	TP53	c.347G>A	p.Arg116Gln (p.R116Q)	NM_001126115.2	SNV	P	46 +	82
	TP53	c.347G>A	p.Arg116Gln (p.R116Q)	NM_001126116.2	SNV	P	46 +	82
	TP53	c.347G>A	p.Arg116Gln (p.R116Q)	NM_001126117.2	SNV	P	46 +	82
	TP53	c.626G>A	p.Arg209Gln (p.R209Q)	NM_001126118.2	SNV	P	46 +	82
	TP53	c.626G>A	p.Arg209Gln (p.R209Q)	NM_001276695.3	SNV	P	46 +	82
	TP53	c.626G>A	p.Arg209Gln (p.R209Q)	NM_001276696.3	SNV	P	46 +	82
	TP53	c.266G>A	p.Arg89Gln (p.R89Q)	NM_001276697.3	SNV	P	46 +	82
	TP53	c.266G>A	p.Arg89Gln (p.R89Q)	NM_001276698.3	SNV	P	46 +	82
	TP53	c.266G>A	p.Arg89Gln (p.R89Q)	NM_001276699.3	SNV	P	46 +	82
	TP53	c.626G>A	p.Arg209Gln (p.R209Q)	NM_001276760.3	SNV	P	46 +	82
	TP53	c.626G>A	p.Arg209Gln (p.R209Q)	NM_001276761.3	SNV	P	46 +	82
12365	TP53	c.733G>A	p.Gly245Ser (p.G245S)	NM_000546.6 M	SNV	P	37 +	72
	TP53	c.733G>A	p.Gly245Ser (p.G245S)	NM_001126112.3	SNV	P	37 +	72
	TP53	c.733G>A	p.Gly245Ser (p.G245S)	NM_001126113.3	SNV	P	37 +	72
	TP53	c.733G>A	p.Gly245Ser (p.G245S)	NM_001126114.3	SNV	P	37 +	72
	TP53	c.337G>A	p.Gly113Ser (p.G113S)	NM_001126115.2	SNV	P	37 +	72

1798 Results, 20 per Page

...

Comparison