"Mayo Clinic Laboratories, Mayo Clinic"[submitter] AND "CAD"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1993842	NM_004341.5(CAD):c.560A>G (p.Tyr187Cys)	CAD (Y187C)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 817700	NM_004341.5(CAD):c.1070_1071del (p.Val357fs)	CAD (V357fs)	Microsatellite (frameshift variant)	not provided	GLikely pathogenic
Select item 1434867	NM_004341.5(CAD):c.1130G>A (p.Arg377His)	CAD (R377H)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2077848	NM_004341.5(CAD):c.2156+5G>A	CAD	Single nucleotide variant (intron variant)	not provided	GUncertain significance
Select item 1450827	NM_004341.5(CAD):c.4471G>A (p.Ala1491Thr)	CAD (A1428T +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1947700	NM_004341.5(CAD):c.4667A>C (p.Lys1556Thr)	CAD (K1556T +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1368987	NM_004341.5(CAD):c.5394+6C>T	CAD	Single nucleotide variant (intron variant)	not provided	GUncertain significance

ClinVar