C3149841[trait identifier] AND "Prenatal Diagnosis Center, Inner Mongo - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1711178	NM_001009944.3(PKD1):c.8098G>A (p.Ala2700Thr)	PKD1 (A2700T)	Single nucleotide variant (missense variant)	Polycystic kidney disease, adult type	GPathogenic
Select item 1711176	NM_001009944.3(PKD1):c.5155G>C (p.Gly1719Arg)	PKD1 (G1719R)	Single nucleotide variant (missense variant)	Polycystic kidney disease, adult type	GPathogenic
Select item 1711177	NM_001009944.3(PKD1):c.4394C>T (p.Pro1465Leu)	PKD1 (P1465L)	Single nucleotide variant (missense variant)	Polycystic kidney disease, adult type	GPathogenic
Select item 1711173	NM_001009944.3(PKD1):c.2545G>A (p.Val849Met)	PKD1 (V849M)	Single nucleotide variant (missense variant)	Polycystic kidney disease, adult type	GPathogenic
Select item 618300	NM_001009944.3(PKD1):c.1198C>T (p.Arg400Ter)	PKD1 (R400*)	Single nucleotide variant (nonsense)	Polycystic kidney disease, adult type +1 more	GPathogenic
Select item 1711174	NM_001009944.3(PKD1):c.616C>T (p.Gln206Ter)	PKD1 (Q206*)	Single nucleotide variant (nonsense)	Polycystic kidney disease, adult type	GPathogenic
Select item 1711175	NM_001009944.3(PKD1):c.191G>C (p.Arg64Pro)	PKD1 (R64P)	Single nucleotide variant (missense variant)	Polycystic kidney disease, adult type	GPathogenic

ClinVar