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Gene: RAC1 & Disease: MRD48, 50 results

ClinVar	Gene	Nucleotide	Amino Acid	Transcript ID	Mutation type	Clinical Significance	Disease count	Publications
445283	RAC1	c.190T>G	p.Tyr64Asp (p.Y64D)	NM_006908.5 M	SNV	P	1 +	2
1699147	RAC1	c.409A>G	p.Ile137Val (p.I137V)	NM_006908.5 M	SNV	VUS	1 +	2
445283	RAC1	c.190T>G	p.Tyr64Asp (p.Y64D)	NM_018890.4	SNV	P	1 +	2
1699147	RAC1	c.466A>G	p.Ile156Val (p.I156V)	NM_018890.4	SNV	VUS	1 +	2
2446363	RAC1	c.181C>G	p.Gln61Glu (p.Q61E)	NM_006908.5 M	SNV	P	1 +	1
2446365	RAC1	c.202C>A	p.Arg68Ser (p.R68S)	NM_006908.5 M	SNV	P	1 +	1
2446366	RAC1	c.202C>G	p.Arg68Gly (p.R68G)	NM_006908.5 M	SNV	P	1 +	1
974895	RAC1	c.198A>T	p.Arg66Ser (p.R66S)	NM_006908.5 M	SNV	LP	1 +	1
1333690	RAC1	c.191A>G	p.Tyr64Cys (p.Y64C)	NM_006908.5 M	SNV	P	1 +	1
1098331	RAC1	c.218C>T	p.Pro73Leu (p.P73L)	NM_006908.5 M	SNV	P	1 +	1
445280	RAC1	c.53G>A	p.Cys18Tyr (p.C18Y)	NM_006908.5 M	SNV	P	1 +	1
445281	RAC1	c.116A>G	p.Asn39Ser (p.N39S)	NM_006908.5 M	SNV	P	1 +	1
445282	RAC1	c.470G>A	p.Cys157Tyr (p.C157Y)	NM_006908.5 M	SNV	P	1 +	1
445284	RAC1	c.151G>A	p.Val51Met (p.V51M)	NM_006908.5 M	SNV	P	1 +	1
445285	RAC1	c.151G>C	p.Val51Leu (p.V51L)	NM_006908.5 M	SNV	P	2 +	1
2446363	RAC1	c.181C>G	p.Gln61Glu (p.Q61E)	NM_018890.4	SNV	P	1 +	1
2446365	RAC1	c.202C>A	p.Arg68Ser (p.R68S)	NM_018890.4	SNV	P	1 +	1
2446366	RAC1	c.202C>G	p.Arg68Gly (p.R68G)	NM_018890.4	SNV	P	1 +	1
974895	RAC1	c.198A>T	p.Arg66Ser (p.R66S)	NM_018890.4	SNV	LP	1 +	1
1333690	RAC1	c.191A>G	p.Tyr64Cys (p.Y64C)	NM_018890.4	SNV	P	1 +	1

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