"Ambry Genetics"[submitter] AND "YAP1"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2326483	NM_001130145.3(YAP1):c.305A>T (p.Lys102Ile)	YAP1 (K102I)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2271317	NM_001130145.3(YAP1):c.434C>G (p.Thr145Ser)	YAP1 (T145S)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2241590	NM_001130145.3(YAP1):c.634G>C (p.Val212Leu)	YAP1 (V34L +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2245370	NM_001130145.3(YAP1):c.638C>A (p.Thr213Lys)	YAP1 (T35K +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2593962	NM_001130145.3(YAP1):c.1004C>T (p.Pro335Leu)	YAP1 (P335L +4 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2474847	NM_001130145.3(YAP1):c.1418G>C (p.Ser473Thr)	YAP1 (S435T +8 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance

ClinVar