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Mutation Direct

Effortless mutation search and display tool

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Gene: RRM2B & Disease: FRTS1, 3 results

ClinVar	Gene	Nucleotide	Amino Acid	Transcript ID	Mutation type	Clinical Significance	Disease count	Publications
977276	RRM2B	c.786G>T	p.Glu262Asp (p.E262D)	NM_015713.5 M	SNV	P	4 +	2
	RRM2B	c.1002G>T	p.Glu334Asp (p.E334D)	NM_001172477.1	SNV	P	4 +	2
	RRM2B	c.630G>T	p.Glu210Asp (p.E210D)	NM_001172478.2	SNV	P	4 +	2

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