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

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3141704	NM_198476.5(ACTMAP):c.1000C>T (p.Arg334Trp)	ACTMAP (R196W +2 more)	Single nucleotide variant (missense variant +3 more)	not specified	GUncertain significance
Select item 3141720	NM_198476.5(ACTMAP):c.979G>A (p.Val327Met)	ACTMAP (V189M +2 more)	Single nucleotide variant (missense variant +3 more)	not specified	GUncertain significance
Select item 3141718	NM_198476.5(ACTMAP):c.494C>T (p.Thr165Met)	ACTMAP (T27M +1 more)	Single nucleotide variant (synonymous variant +2 more)	not specified	GUncertain significance
Select item 3141714	NM_198476.5(ACTMAP):c.469C>T (p.Arg157Trp)	ACTMAP (T26M +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3141711	NM_198476.5(ACTMAP):c.451C>T (p.Pro151Ser)	ACTMAP (P20L +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3141708	NM_198476.5(ACTMAP):c.187G>A (p.Ala63Thr)	ACTMAP (A63T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

ClinVar