CDA[gene] and "single gene"[properties] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3140732	NM_001785.3(CDA):c.116G>C (p.Gly39Ala)	CDA (G39A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 784935	NM_001785.3(CDA):c.183G>A (p.Pro61=)	CDA	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 737822	NM_001785.3(CDA):c.210T>C (p.Ala70=)	CDA	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 2589304	NM_001785.3(CDA):c.259A>C (p.Ile87Leu)	CDA (I87L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2391428	NM_001785.3(CDA):c.286A>G (p.Ile96Val)	CDA (I96V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3140733	NM_001785.3(CDA):c.351G>A (p.Met117Ile)	CDA (M117I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2323803	NM_001785.3(CDA):c.359C>T (p.Pro120Leu)	CDA (P120L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2408531	NM_001785.3(CDA):c.368C>T (p.Thr123Met)	CDA (T123M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3264914	NM_001785.3(CDA):c.383C>T (p.Thr128Met)	CDA (T128M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

ClinVar