"Ambry Genetics"[submitter] AND "DOLPP1"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3085209	NM_020438.5(DOLPP1):c.16C>G (p.Gln6Glu)	DOLPP1, LOC130002736 (Q6E)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3085211	NM_020438.5(DOLPP1):c.91C>T (p.His31Tyr)	DOLPP1 (H31Y)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3085210	NM_020438.5(DOLPP1):c.233A>C (p.Asn78Thr)	DOLPP1 (N78T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3273492	NM_020438.5(DOLPP1):c.517G>A (p.Gly173Ser)	DOLPP1 (G173S)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2297268	NM_020438.5(DOLPP1):c.556G>T (p.Val186Phe)	DOLPP1 (V186F)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2462742	NM_020438.5(DOLPP1):c.569T>G (p.Leu190Arg)	DOLPP1 (L190R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2216885	NM_020438.5(DOLPP1):c.640G>A (p.Val214Ile)	DOLPP1 (V214I +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2338080	NM_020438.5(DOLPP1):c.685A>G (p.Arg229Gly)	DOLPP1 (R186G +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

ClinVar