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检索条件：

基因: TP53 & 疾病: BMFS5, 共354条

ClinVar	基因	碱基改变	氨基酸改变	转录本ID	突变类型	临床意义	疾病数量	文献数量
12379	TP53	c.1010G>A	p.Arg337His (p.R337H)	NM_000546.6 M	SNV	致病突变	16 +	77
	TP53	c.1010G>A	p.Arg337His (p.R337H)	NM_001126112.3	SNV	致病突变	16 +	77
	TP53	c.*29G>A	--	NM_001126113.3	SNV	致病突变	16 +	77
	TP53	c.*117G>A	--	NM_001126114.3	SNV	致病突变	16 +	77
	TP53	c.614G>A	p.Arg205His (p.R205H)	NM_001126115.2	SNV	致病突变	16 +	77
	TP53	c.*117G>A	--	NM_001126116.2	SNV	致病突变	16 +	77
	TP53	c.*29G>A	--	NM_001126117.2	SNV	致病突变	16 +	77
	TP53	c.893G>A	p.Arg298His (p.R298H)	NM_001126118.2	SNV	致病突变	16 +	77
	TP53	c.*29G>A	--	NM_001276695.3	SNV	致病突变	16 +	77
	TP53	c.*117G>A	--	NM_001276696.3	SNV	致病突变	16 +	77
	TP53	c.533G>A	p.Arg178His (p.R178H)	NM_001276697.3	SNV	致病突变	16 +	77
	TP53	c.*117G>A	--	NM_001276698.3	SNV	致病突变	16 +	77
	TP53	c.*29G>A	--	NM_001276699.3	SNV	致病突变	16 +	77
	TP53	c.893G>A	p.Arg298His (p.R298H)	NM_001276760.3	SNV	致病突变	16 +	77
	TP53	c.893G>A	p.Arg298His (p.R298H)	NM_001276761.3	SNV	致病突变	16 +	77
12365	TP53	c.733G>A	p.Gly245Ser (p.G245S)	NM_000546.6 M	SNV	致病突变	37 +	72
	TP53	c.733G>A	p.Gly245Ser (p.G245S)	NM_001126112.3	SNV	致病突变	37 +	72
	TP53	c.733G>A	p.Gly245Ser (p.G245S)	NM_001126113.3	SNV	致病突变	37 +	72
	TP53	c.733G>A	p.Gly245Ser (p.G245S)	NM_001126114.3	SNV	致病突变	37 +	72
	TP53	c.337G>A	p.Gly113Ser (p.G113S)	NM_001126115.2	SNV	致病突变	37 +	72

共354个结果, 每页展示20条

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