"Ambry Genetics"[submitter] AND "LOC130003219"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3296466	NM_019046.3(ANKRD16):c.154G>T (p.Val52Leu)	ANKRD16, LOC130003219 (V52L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2217906	NM_019046.3(ANKRD16):c.127T>C (p.Cys43Arg)	ANKRD16, LOC130003219 (C43R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2208886	NM_019046.3(ANKRD16):c.118C>G (p.Leu40Val)	ANKRD16, LOC130003219 (L40V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2218478	NM_019046.3(ANKRD16):c.106G>A (p.Ala36Thr)	ANKRD16, LOC130003219 (A36T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3123261	NM_019046.3(ANKRD16):c.104C>G (p.Pro35Arg)	ANKRD16, LOC130003219 (P35R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2570383	NM_019046.3(ANKRD16):c.40G>A (p.Val14Met)	ANKRD16, LOC130003219 (V14M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2237678	NM_019046.3(ANKRD16):c.20C>T (p.Pro7Leu)	ANKRD16, LOC130003219 (P7L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

ClinVar