Related gene-specific medical variations for Gene (Select 22979) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3274712	NM_014971.2(EFR3B):c.937G>A (p.Val313Met)	EFR3B, LOC122756672 (V313M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2212484	NM_014971.2(EFR3B):c.871A>C (p.Ile291Leu)	EFR3B, LOC122756672 (I256L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance