Related gene-specific medical variations for Gene (Select 51616) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3324299	NM_015975.5(TAF9B):c.8C>T (p.Ser3Leu)	LOC130068465, TAF9B (S3L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3173594	NM_015975.5(TAF9B):c.45T>A (p.Asp15Glu)	LOC130068465, TAF9B (D15E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2247860	NM_015975.5(TAF9B):c.37C>G (p.Pro13Ala)	LOC130068465, TAF9B (P13A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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