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检索条件：

基因: EGFR & 疾病: GBM, 共88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
45225	EGFR	c.2156G>C	p.Gly719Ala (p.G719A)	NM_005228.5 M	SNV	致病突变	5 +	18
	EGFR	c.2021G>C	p.Gly674Ala (p.G674A)	NM_001346897.2	SNV	致病突变	5 +	18
	EGFR	c.2156G>C	p.Gly719Ala (p.G719A)	NM_001346898.2	SNV	致病突变	5 +	18
	EGFR	c.2021G>C	p.Gly674Ala (p.G674A)	NM_001346899.2	SNV	致病突变	5 +	18
	EGFR	c.1997G>C	p.Gly666Ala (p.G666A)	NM_001346900.2	SNV	致病突变	5 +	18
	EGFR	c.1355G>C	p.Gly452Ala (p.G452A)	NM_001346941.2	SNV	致病突变	5 +	18
16611	EGFR	c.2155G>T	p.Gly719Cys (p.G719C)	NM_005228.5 M	SNV	致病突变	5 +	16
	EGFR	c.2020G>T	p.Gly674Cys (p.G674C)	NM_001346897.2	SNV	致病突变	5 +	16
	EGFR	c.2155G>T	p.Gly719Cys (p.G719C)	NM_001346898.2	SNV	致病突变	5 +	16
	EGFR	c.2020G>T	p.Gly674Cys (p.G674C)	NM_001346899.2	SNV	致病突变	5 +	16
	EGFR	c.1996G>T	p.Gly666Cys (p.G666C)	NM_001346900.2	SNV	致病突变	5 +	16
	EGFR	c.1354G>T	p.Gly452Cys (p.G452C)	NM_001346941.2	SNV	致病突变	5 +	16
376075	EGFR	c.2156G>A	p.Gly719Asp (p.G719D)	NM_005228.5 M	SNV	可能致病	6 +	5
	EGFR	c.2021G>A	p.Gly674Asp (p.G674D)	NM_001346897.2	SNV	可能致病	6 +	5
	EGFR	c.2156G>A	p.Gly719Asp (p.G719D)	NM_001346898.2	SNV	可能致病	6 +	5
	EGFR	c.2021G>A	p.Gly674Asp (p.G674D)	NM_001346899.2	SNV	可能致病	6 +	5
	EGFR	c.1997G>A	p.Gly666Asp (p.G666D)	NM_001346900.2	SNV	可能致病	6 +	5
	EGFR	c.1355G>A	p.Gly452Asp (p.G452D)	NM_001346941.2	SNV	可能致病	6 +	5
376209	EGFR	c.866C>T	p.Ala289Val (p.A289V)	NM_005228.5 M	SNV	可能致病	5 +	2
376210	EGFR	c.1793G>T	p.Gly598Val (p.G598V)	NM_005228.5 M	SNV	可能致病	5 +	2

共88个结果, 每页展示20条

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