Related gene-specific medical variations for Gene (Select 6498) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3318746	NM_005414.5(SKIL):c.1300A>T (p.Ile434Leu)	LOC129389168, SKIL (I434L +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3162683	NM_005414.5(SKIL):c.1372C>T (p.Leu458Phe)	LOC129389168, SKIL (L458F +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3162682	NM_005414.5(SKIL):c.1369T>C (p.Ser457Pro)	LOC129389168, SKIL (S437P +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3162681	NM_005414.5(SKIL):c.1310A>T (p.Gln437Leu)	LOC129389168, SKIL (Q417L +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2339907	NM_005414.5(SKIL):c.1207T>C (p.Tyr403His)	LOC129389168, SKIL (Y403H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 161532	NM_005414.5(SKIL):c.942A>T (p.Arg314Ser)	SKIL (R314S +1 more)	Single nucleotide variant (missense variant)	Malignant tumor of prostate	GUncertain significance

ClinVar