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Gene: DHFR & Disease: DHFRD, 39 results

ClinVar	Gene	Nucleotide	Amino Acid	Transcript ID	Mutation type	Clinical Significance	Disease count	Publications
29674	DHFR	c.458A>T	p.Asp153Val (p.D153V)	NM_000791.4 M	SNV	P	1 +	4
	DHFR	c.302A>T	p.Asp101Val (p.D101V)	NM_001290354.2	SNV	P	1 +	4
	DHFR	c.369+3979A>T	--	NM_001290357.2	SNV	P	1 +	4
635180	DHFR	c.-416C>G	--	NM_000791.4 M	SNV	LB	2 +	2
	DHFR	c.-522C>G	--	NM_001290354.2	SNV	LB	2 +	2
	DHFR	c.-416C>G	--	NM_001290357.2	SNV	LB	2 +	2
29673	DHFR	c.238C>T	p.Leu80Phe (p.L80F)	NM_000791.4 M	SNV	P	1 +	1
	DHFR	c.82C>T	p.Leu28Phe (p.L28F)	NM_001290354.2	SNV	P	1 +	1
	DHFR	c.238C>T	p.Leu80Phe (p.L80F)	NM_001290357.2	SNV	P	1 +	1
790792	DHFR	c.-418GGCCGCTGC[1]	--	NM_000791.4 M	MS	LB	1 +	0
790792	DHFR	c.-409_-401delGGCCGCTGC	--	NM_000791.4 M	MS	LB	1 +	0
402590	DHFR	c.-442_-434del	--	NM_000791.4 M	Del	B	1 +	0
402591	DHFR	c.-473T>C	--	NM_000791.4 M	SNV	B	1 +	0
218608	DHFR	c.-437GGGGCGCTG[3]	--	NM_000791.4 M	MS	LB	1 +	0
218608	DHFR	c.-428_-420dupGGGGCGCTG	--	NM_000791.4 M	MS	LB	1 +	0
710203	DHFR	c.-406CGCTGCAGC[1]	--	NM_000791.4 M	MS	LB	1 +	0
710203	DHFR	c.-397_-389delCGCTGCAGC	--	NM_000791.4 M	MS	LB	1 +	0
769652	DHFR	c.-409_-392del	--	NM_000791.4 M	Del	LB	2 +	0
1709841	DHFR	c.335T>G	p.Met112Arg (p.M112R)	NM_000791.4 M	SNV	VUS	1 +	0
778197	DHFR	c.-259C>T	--	NM_000791.4 M	SNV	LB	1 +	0

39 Results, 20 per Page

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