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

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Items: 26

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2531537	NM_003631.5(PARG):c.2914C>A (p.Gln972Lys)	PARG (Q972K +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2510283	NM_003631.5(PARG):c.2903A>G (p.Asp968Gly)	PARG (D968G +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3208652	NM_003631.5(PARG):c.2846A>T (p.Asp949Val)	PARG (D841V +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3208651	NM_003631.5(PARG):c.2801G>A (p.Arg934Gln)	PARG (R520Q +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2354976	NM_003631.5(PARG):c.2731A>G (p.Ile911Val)	PARG (I803V +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2373478	NM_003631.5(PARG):c.2659A>T (p.Ile887Leu)	PARG (I473L +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2295823	NM_003631.5(PARG):c.2561G>A (p.Arg854His)	PARG (R772H +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2518578	NM_003631.5(PARG):c.2560C>T (p.Arg854Cys)	PARG (R772C +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3208650	NM_003631.5(PARG):c.2472C>G (p.Ile824Met)	PARG (I716M +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3208649	NM_003631.5(PARG):c.2446C>T (p.Arg816Trp)	PARG (R816W +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2349399	NM_003631.5(PARG):c.2398C>T (p.Arg800Cys)	PARG (R800C +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3208648	NM_003631.5(PARG):c.2222G>A (p.Arg741His)	PARG (R327H +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2349970	NM_003631.5(PARG):c.2167G>A (p.Glu723Lys)	PARG (E641K +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2348952	NM_003631.5(PARG):c.2150G>A (p.Arg717Gln)	PARG (R717Q +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2596481	NM_003631.5(PARG):c.1991T>C (p.Leu664Ser)	PARG (L582S +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2590390	NM_003631.5(PARG):c.1861C>T (p.His621Tyr)	PARG (H207Y +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3208647	NM_003631.5(PARG):c.1834A>G (p.Ile612Val)	PARG (I530V +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2245814	NM_003631.5(PARG):c.1712C>A (p.Thr571Lys)	PARG (T463K +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2404281	NM_003631.5(PARG):c.1641T>A (p.Phe547Leu)	PARG (F133L +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2394736	NM_003631.5(PARG):c.1635C>A (p.Asn545Lys)	PARG (N437K +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2292093	NM_003631.5(PARG):c.1612C>G (p.Leu538Val)	PARG (L124V +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3208646	NM_003631.5(PARG):c.1601G>A (p.Ser534Asn)	PARG (S120N +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2589052	NM_003631.5(PARG):c.1513T>A (p.Leu505Met)	PARG (L397M +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2458763	NM_003631.5(PARG):c.1457T>G (p.Val486Gly)	PARG (V404G +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2256078	NM_003631.5(PARG):c.1124G>A (p.Ser375Asn)	PARG (S267N +2 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2376555	NM_003631.5(PARG):c.1046C>G (p.Ala349Gly)	PARG (A241G +2 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance

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Items: 26