"Ambry Genetics"[submitter] AND "FUNDC2"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2276085	NM_023934.4(FUNDC2):c.23C>A (p.Ala8Asp)	FUNDC2 (A8D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2496211	NM_023934.4(FUNDC2):c.37G>A (p.Val13Met)	FUNDC2 (V13M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2352260	NM_023934.4(FUNDC2):c.55C>T (p.His19Tyr)	FUNDC2 (H19Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3097447	NM_023934.4(FUNDC2):c.103A>C (p.Lys35Gln)	FUNDC2, LOC130068894 (K35Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2380588	NM_023934.4(FUNDC2):c.127A>G (p.Ser43Gly)	FUNDC2, LOC130068894 (S43G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2251007	NM_023934.4(FUNDC2):c.211G>A (p.Gly71Arg)	FUNDC2 (G71R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2249337	NM_023934.4(FUNDC2):c.347T>G (p.Phe116Cys)	FUNDC2 (F116C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3280172	NM_023934.4(FUNDC2):c.446G>A (p.Arg149His)	FUNDC2 (R149H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

ClinVar