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Gene: MYH3 & Disease: DA2B1, 159 results

ClinVar	Gene	Nucleotide	Amino Acid	Transcript ID	Mutation type	Clinical Significance	Disease count	Publications
129649	MYH3	c.2151C>A	p.Gly717= (p.G717=)	NM_002470.4 M	SNV	B	5 +	3
129652	MYH3	c.2916A>G	p.Thr972= (p.T972=)	NM_002470.4 M	SNV	B	5 +	3
129653	MYH3	c.2952T>C	p.Ser984= (p.S984=)	NM_002470.4 M	SNV	B	5 +	3
129656	MYH3	c.3138A>C	p.Arg1046= (p.R1046=)	NM_002470.4 M	SNV	B	5 +	3
129657	MYH3	c.3348T>C	p.Ile1116= (p.I1116=)	NM_002470.4 M	SNV	B	2 +	3
129658	MYH3	c.3574G>A	p.Ala1192Thr (p.A1192T)	NM_002470.4 M	SNV	B	5 +	3
129663	MYH3	c.4731C>T	p.Ile1577= (p.I1577=)	NM_002470.4 M	SNV	B	5 +	3
321727	MYH3	c.4172+9C>T	--	NM_002470.4 M	SNV	LB	2 +	2
321746	MYH3	c.2683-14C>A	--	NM_002470.4 M	SNV	LB	2 +	2
321772	MYH3	c.252G>A	p.Lys84= (p.K84=)	NM_002470.4 M	SNV	LB	2 +	2
321773	MYH3	c.248C>G	p.Pro83Arg (p.P83R)	NM_002470.4 M	SNV	B	2 +	2
211552	MYH3	c.3592G>A	p.Ala1198Thr (p.A1198T)	NM_002470.4 M	SNV	LB	2 +	2
211555	MYH3	c.4910C>T	p.Ala1637Val (p.A1637V)	NM_002470.4 M	SNV	LB	2 +	2
211557	MYH3	c.875C>G	p.Ser292Cys (p.S292C)	NM_002470.4 M	SNV	LP	1 +	2
258670	MYH3	c.1575C>T	p.Ile525= (p.I525=)	NM_002470.4 M	SNV	LB	5 +	2
258671	MYH3	c.1581+13A>C	--	NM_002470.4 M	SNV	B	5 +	2
129648	MYH3	c.2106C>T	p.Gly702= (p.G702=)	NM_002470.4 M	SNV	LB	2 +	2
258673	MYH3	c.2166-15A>G	--	NM_002470.4 M	SNV	B	5 +	2
129651	MYH3	c.2610A>G	p.Lys870= (p.K870=)	NM_002470.4 M	SNV	LB	2 +	2
258674	MYH3	c.2683-4T>C	--	NM_002470.4 M	SNV	LB	2 +	2

159 Results, 20 per Page

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