Related gene-specific medical variations for Gene (Select 373863) - ClinVar - NCBI

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Items: 11

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3273155	NM_194249.3(DND1):c.906C>A (p.Ser302Arg)	DND1, WDR55 (S302R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3273153	NM_194249.3(DND1):c.701G>A (p.Arg234Gln)	WDR55, DND1 (R234Q)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 3084648	NM_194249.3(DND1):c.974C>A (p.Ser325Tyr)	DND1, WDR55 (S325Y)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3084647	NM_194249.3(DND1):c.910C>G (p.Leu304Val)	DND1, WDR55 (L304V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3084645	NM_194249.3(DND1):c.758A>G (p.Gln253Arg)	DND1, WDR55 (Q253R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3084644	NM_194249.3(DND1):c.692C>T (p.Pro231Leu)	DND1, WDR55 (P231L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3084643	NM_194249.3(DND1):c.668G>A (p.Arg223Gln)	DND1, WDR55 (R223Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2550707	NM_194249.3(DND1):c.842G>A (p.Gly281Glu)	DND1, WDR55 (G281E)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2515573	NM_194249.3(DND1):c.830G>A (p.Cys277Tyr)	DND1, WDR55 (C277Y)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2276783	NM_194249.3(DND1):c.827A>G (p.Lys276Arg)	DND1, WDR55 (K276R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2272049	NM_194249.3(DND1):c.951T>A (p.His317Gln)	DND1, WDR55 (H317Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance