"GeneDx"[submitter] AND "YY1AP1"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 145877	GRCh38/hg38 1q22(chr1:155648847-155715659)x3	DAP3, LOC129931572 +2 more	Copy number gain	See cases	GLikely benign
Select item 3371308	NM_139119.3(YY1AP1):c.1877del (p.Pro626fs)	YY1AP1 (P560fs +6 more)	Deletion (frameshift variant +1 more)	not provided	GLikely pathogenic
Select item 2499233	NM_139119.3(YY1AP1):c.1303del (p.Gln435fs)	YY1AP1 (Q369fs +6 more)	Deletion (frameshift variant +1 more)	not provided	GUncertain significance
Select item 1309755	NM_139119.3(YY1AP1):c.567A>T (p.Lys189Asn)	YY1AP1 (K123N +4 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1312653	NM_139119.3(YY1AP1):c.403A>G (p.Ile135Val)	YY1AP1 (I124V +4 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1723831	NM_139119.3(YY1AP1):c.-27C>T	DAP3, YY1AP1 (R130* +1 more)	Single nucleotide variant (5 prime UTR variant +2 more)	not provided	GLikely pathogenic
Select item 253835	GRCh37/hg19 1q22(chr1:155412745-155755215)x3	YY1AP1, ASH1L +3 more	Copy number gain	See cases	GUncertain significance

ClinVar