"PreventionGenetics, part of Exact Sciences"[submitter] AND "YAP1"[gen - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2884801	NM_001130145.3(YAP1):c.129_140del (p.Ala44_Ala47del)	YAP1	Deletion (inframe_deletion)	YAP1-related condition +1 more	GUncertain significance
Select item 725467	NM_001130145.3(YAP1):c.204C>G (p.Leu68=)	YAP1	Single nucleotide variant (synonymous variant)	YAP1-related condition +1 more	GLikely benign
Select item 2634825	NM_001130145.3(YAP1):c.313T>C (p.Ser105Pro)	YAP1 (S105P)	Single nucleotide variant (missense variant)	not provided +2 more	GUncertain significance
Select item 3044203	NM_001130145.3(YAP1):c.321+8C>T	YAP1	Single nucleotide variant (intron variant)	YAP1-related condition	GLikely benign
Select item 802714	NM_001130145.3(YAP1):c.832C>T (p.Pro278Ser)	YAP1 (P100S +2 more)	Single nucleotide variant (missense variant)	Uveal coloboma-cleft lip and palate-intellectual disability +2 more	GLikely benign
Select item 3059192	NM_001130145.3(YAP1):c.879C>T (p.Gly293=)	YAP1	Single nucleotide variant (synonymous variant)	YAP1-related condition	GLikely benign
Select item 789314	NM_001130145.3(YAP1):c.1104C>T (p.Pro368=)	YAP1	Single nucleotide variant (synonymous variant)	YAP1-related condition +1 more	GBenign/Likely benign
Select item 778560	NM_001130145.3(YAP1):c.1277-4C>T	YAP1	Single nucleotide variant (intron variant)	YAP1-related condition +1 more	GBenign

ClinVar