"CeGaT Center for Human Genetics Tuebingen"[submitter] AND "ULK3"[gene - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2645547	NM_001099436.4(ULK3):c.852A>G (p.Ala284=)	ULK3	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2645548	NM_001099436.4(ULK3):c.498G>A (p.Pro166=)	ULK3	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2645549	NM_001099436.4(ULK3):c.295C>T (p.Leu99=)	ULK3	Single nucleotide variant (synonymous variant +2 more)	not provided	GLikely benign
Select item 2645550	NM_001099436.4(ULK3):c.93C>T (p.Ala31=)	ULK3	Single nucleotide variant (synonymous variant +2 more)	not provided	GLikely benign
Select item 2498630	GRCh37/hg19 15q22.33-26.1(chr15:67358491-91644328)x3	ISLR2, MESD +209 more	Copy number gain	not provided	GPathogenic
Select item 369835	GRCh37/hg19 15q22.1-26.3(chr15:59297293-102480888)x3	SLC24A1, SLC28A1 +310 more	Copy number gain	not provided	GLikely pathogenic

ClinVar