Related gene-specific medical variations for Gene (Select 10291) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3160797	NM_005877.6(SF3A1):c.38C>T (p.Pro13Leu)	CCDC157, LOC130067209 +1 more (P13L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2386437	NM_005877.6(SF3A1):c.29C>T (p.Pro10Leu)	CCDC157, LOC130067209 +1 more (P10L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance