Related gene-specific medical variations for Gene (Select 317781) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3271359	NM_175066.4(DDX51):c.106G>A (p.Glu36Lys)	DDX51, LOC130009246 (E36K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3271353	NM_175066.4(DDX51):c.86G>A (p.Gly29Asp)	DDX51, LOC130009246 (G29D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3081108	NM_175066.4(DDX51):c.94C>T (p.Arg32Cys)	DDX51, LOC130009246 (R32C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3081099	NM_175066.4(DDX51):c.214C>G (p.Arg72Gly)	DDX51, LOC130009245 (R72G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2373513	NM_175066.4(DDX51):c.56G>A (p.Gly19Glu)	DDX51, LOC130009247 (G19E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2254501	NM_175066.4(DDX51):c.208C>T (p.Pro70Ser)	DDX51, LOC130009245 (P70S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

ClinVar