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Gene: GRIN2B & Disease: MRD6, 1173 results

ClinVar	Gene	Nucleotide	Amino Acid	Transcript ID	Mutation type	Clinical Significance	Disease count	Publications
208643	GRIN2B	c.2459G>C	p.Gly820Ala (p.G820A)	NM_000834.5 M	SNV	P	3 +	7
916598	GRIN2B	c.1382G>T	p.Cys461Phe (p.C461F)	NM_000834.5 M	SNV	P	1 +	6
224818	GRIN2B	c.2065G>A	p.Gly689Ser (p.G689S)	NM_000834.5 M	SNV	P	3 +	5
580700	GRIN2B	c.2459G>A	p.Gly820Glu (p.G820E)	NM_000834.5 M	SNV	P	3 +	5
374226	GRIN2B	c.2116A>G	p.Met706Val (p.M706V)	NM_000834.5 M	SNV	P	3 +	4
98436	GRIN2B	c.2691C>T	p.Asn897= (p.N897=)	NM_000834.5 M	SNV	LB	2 +	3
205703	GRIN2B	c.3552C>T	p.Gly1184= (p.G1184=)	NM_000834.5 M	SNV	LB	2 +	3
205720	GRIN2B	c.3747C>T	p.Gly1249= (p.G1249=)	NM_000834.5 M	SNV	LB	2 +	3
205732	GRIN2B	c.3799G>T	p.Ala1267Ser (p.A1267S)	NM_000834.5 M	SNV	LB	2 +	3
411106	GRIN2B	c.4105G>A	p.Gly1369Ser (p.G1369S)	NM_000834.5 M	SNV	LB	2 +	3
98431	GRIN2B	c.4218C>T	p.Phe1406= (p.F1406=)	NM_000834.5 M	SNV	B	2 +	3
98432	GRIN2B	c.4197T>C	p.His1399= (p.H1399=)	NM_000834.5 M	SNV	LB	2 +	3
129200	GRIN2B	c.1665C>T	p.Ser555= (p.S555=)	NM_000834.5 M	SNV	LB	2 +	3
129204	GRIN2B	c.3534C>T	p.His1178= (p.H1178=)	NM_000834.5 M	SNV	LB	2 +	3
129203	GRIN2B	c.3498C>T	p.Ser1166= (p.S1166=)	NM_000834.5 M	SNV	LB	2 +	3
39661	GRIN2B	c.1658C>T	p.Pro553Leu (p.P553L)	NM_000834.5 M	SNV	P	2 +	3
245764	GRIN2B	c.4312G>A	p.Val1438Met (p.V1438M)	NM_000834.5 M	SNV	B	2 +	2
98433	GRIN2B	c.3648C>T	p.Arg1216= (p.R1216=)	NM_000834.5 M	SNV	LB	2 +	2
98437	GRIN2B	c.2664C>T	p.Thr888= (p.T888=)	NM_000834.5 M	SNV	LB	2 +	2
98442	GRIN2B	c.15G>A	p.Ala5= (p.A5=)	NM_000834.5 M	SNV	LB	2 +	2

共1173个结果, 每页展示20条

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