"Genome Diagnostics Laboratory, University Medical Center Utrecht"[sub - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1328049	NM_138295.5(PKD1L1):c.7795A>G (p.Met2599Val)	PKD1L1, PKD1L1-AS1 (M2599V)	Single nucleotide variant (missense variant)	not provided +1 more	GLikely benign
Select item 732966	NM_138295.5(PKD1L1):c.5108G>A (p.Arg1703His)	PKD1L1 (R1703H)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 1285159	NM_138295.5(PKD1L1):c.3845T>A (p.Val1282Glu)	PKD1L1 (V1282E)	Single nucleotide variant (missense variant)	not provided +2 more	GUncertain significance
Select item 715847	NM_138295.5(PKD1L1):c.2979A>T (p.Ser993=)	PKD1L1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 777629	NM_138295.5(PKD1L1):c.2675+4C>T	PKD1L1	Single nucleotide variant (intron variant)	not provided +1 more	GBenign/Likely benign
Select item 717522	NM_138295.5(PKD1L1):c.908G>A (p.Arg303Gln)	PKD1L1 (R303Q)	Single nucleotide variant (missense variant)	not provided	GBenign/Likely benign

ClinVar