Related gene-specific medical variations for Gene (Select 8446) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3505816	NM_003584.3(DUSP11):c.79G>C (p.Gly27Arg)	DUSP11, LOC129934093 (G27R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3505811	NM_003584.3(DUSP11):c.-77C>T	DUSP11, LOC129934094 (S22F)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3274041	NM_003584.3(DUSP11):c.-98G>C	DUSP11, LOC129934094 (R15P)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3086260	NM_003584.3(DUSP11):c.-56C>T	DUSP11, LOC129934094 (A29V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3086257	NM_003584.3(DUSP11):c.-72C>T	DUSP11, LOC129934094 (P24S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3086255	NM_003584.3(DUSP11):c.-86G>A	DUSP11, LOC129934094 (C19Y)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2410176	NM_003584.3(DUSP11):c.-36G>A	DUSP11, LOC129934094	Single nucleotide variant (5 prime UTR variant)	not specified	GUncertain significance
Select item 2313883	NM_003584.3(DUSP11):c.82G>A (p.Gly28Arg)	DUSP11, LOC129934093 (G28R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

ClinVar