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

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Items: 72

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2605484	NM_002864.3(PZP):c.4301G>A (p.Ser1434Asn)	KLRG1, PZP (S1434N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2610904	NM_002864.3(PZP):c.4249A>T (p.Ser1417Cys)	KLRG1, PZP (S1417C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3311918	NM_002864.3(PZP):c.4178C>A (p.Ser1393Tyr)	KLRG1, PZP (S1393Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3150283	NM_002864.3(PZP):c.4170G>T (p.Lys1390Asn)	KLRG1, PZP (K1390N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3150282	NM_002864.3(PZP):c.4097G>A (p.Ser1366Asn)	KLRG1, PZP (S1366N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2209156	NM_002864.3(PZP):c.3915A>C (p.Leu1305Phe)	KLRG1, PZP (L1305F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3150280	NM_002864.3(PZP):c.3881C>T (p.Thr1294Ile)	KLRG1, PZP (T1294I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2459167	NM_002864.3(PZP):c.3734T>C (p.Met1245Thr)	KLRG1, PZP (M1245T)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2610594	NM_002864.3(PZP):c.3646T>A (p.Ser1216Thr)	KLRG1, PZP (S1216T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2472723	NM_002864.3(PZP):c.3599G>C (p.Gly1200Ala)	KLRG1, PZP (G1200A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3150279	NM_002864.3(PZP):c.3559G>A (p.Val1187Ile)	KLRG1, PZP (V1187I)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2560451	NM_002864.3(PZP):c.3517C>A (p.Leu1173Met)	KLRG1, PZP (L1173M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3311916	NM_002864.3(PZP):c.3476C>T (p.Ala1159Val)	KLRG1, PZP (A1159V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3311915	NM_002864.3(PZP):c.3465G>T (p.Leu1155Phe)	KLRG1, PZP (L1155F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2409106	NM_002864.3(PZP):c.3383G>A (p.Arg1128His)	KLRG1, PZP (R1128H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2529826	NM_002864.3(PZP):c.3329A>G (p.Tyr1110Cys)	KLRG1, PZP (Y1110C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2206198	NM_002864.3(PZP):c.3254G>A (p.Cys1085Tyr)	KLRG1, PZP (C1085Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3150277	NM_002864.3(PZP):c.3196G>A (p.Glu1066Lys)	KLRG1, PZP (E1066K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3311912	NM_002864.3(PZP):c.3167C>T (p.Ala1056Val)	KLRG1, PZP (A1056V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3311917	NM_002864.3(PZP):c.3164T>A (p.Phe1055Tyr)	KLRG1, PZP (F1055Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2540438	NM_002864.3(PZP):c.2983T>A (p.Tyr995Asn)	KLRG1, PZP (Y995N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3150276	NM_002864.3(PZP):c.2903T>C (p.Ile968Thr)	KLRG1, PZP (I968T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3150275	NM_002864.3(PZP):c.2902A>G (p.Ile968Val)	KLRG1, PZP (I968V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3150274	NM_002864.3(PZP):c.2738C>T (p.Ala913Val)	KLRG1, PZP (A913V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2478090	NM_002864.3(PZP):c.2637T>A (p.Ser879Arg)	KLRG1, PZP (S879R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2619749	NM_002864.3(PZP):c.2602C>A (p.Pro868Thr)	KLRG1, PZP (P868T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2485953	NM_002864.3(PZP):c.2528C>T (p.Ser843Phe)	KLRG1, PZP (S843F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2320335	NM_002864.3(PZP):c.2493T>G (p.Ser831Arg)	KLRG1, PZP (S831R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2595488	NM_002864.3(PZP):c.2429G>A (p.Arg810His)	PZP, KLRG1 (R810H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2358643	NM_002864.3(PZP):c.2333T>C (p.Leu778Pro)	KLRG1, PZP (L778P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3150273	NM_002864.3(PZP):c.2320G>A (p.Gly774Arg)	KLRG1, PZP (G774R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2275494	NM_002864.3(PZP):c.2308G>A (p.Glu770Lys)	KLRG1, PZP (E770K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3150272	NM_002864.3(PZP):c.2249T>C (p.Val750Ala)	KLRG1, PZP (V750A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2508644	NM_002864.3(PZP):c.2218T>G (p.Tyr740Asp)	KLRG1, PZP (Y740D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2553050	NM_002864.3(PZP):c.2195C>T (p.Pro732Leu)	KLRG1, PZP (P732L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2326619	NM_002864.3(PZP):c.2083G>C (p.Ala695Pro)	KLRG1, PZP (A695P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3150270	NM_002864.3(PZP):c.2060T>A (p.Val687Asp)	KLRG1, PZP (V687D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2568316	NM_002864.3(PZP):c.1871C>T (p.Thr624Ile)	KLRG1, PZP (T624I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3150269	NM_002864.3(PZP):c.1820C>T (p.Ala607Val)	KLRG1, PZP (A607V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2322811	NM_002864.3(PZP):c.1768C>A (p.Leu590Ile)	KLRG1, PZP (L590I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2488278	NM_002864.3(PZP):c.1753G>C (p.Ala585Pro)	KLRG1, PZP (A585P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3150268	NM_002864.3(PZP):c.1750G>A (p.Ala584Thr)	KLRG1, PZP (A584T)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3311913	NM_002864.3(PZP):c.1608G>A (p.Met536Ile)	KLRG1, PZP (M536I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2221623	NM_002864.3(PZP):c.1562C>T (p.Ala521Val)	KLRG1, PZP (A521V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2375344	NM_002864.3(PZP):c.1534G>C (p.Glu512Gln)	KLRG1, PZP (E512Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3150267	NM_002864.3(PZP):c.1492A>C (p.Lys498Gln)	KLRG1, PZP (K498Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2517424	NM_002864.3(PZP):c.1474C>T (p.His492Tyr)	KLRG1, PZP (H492Y)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2482020	NM_002864.3(PZP):c.1469G>T (p.Ser490Ile)	KLRG1, PZP (S490I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2565704	NM_002864.3(PZP):c.1337G>A (p.Arg446His)	KLRG1, PZP (R446H)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3150266	NM_002864.3(PZP):c.1311C>A (p.His437Gln)	KLRG1, PZP (H437Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2541447	NM_002864.3(PZP):c.1307A>G (p.Asp436Gly)	KLRG1, PZP (D436G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3150264	NM_002864.3(PZP):c.1216A>G (p.Asn406Asp)	KLRG1, PZP (N406D)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3150263	NM_002864.3(PZP):c.1201G>C (p.Ala401Pro)	KLRG1, PZP (A401P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2314469	NM_002864.3(PZP):c.1196G>T (p.Gly399Val)	KLRG1, PZP (G399V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2271145	NM_002864.3(PZP):c.1077C>G (p.Ile359Met)	KLRG1, PZP (I359M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2293130	NM_002864.3(PZP):c.937G>C (p.Glu313Gln)	KLRG1, PZP (E313Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2293129	NM_002864.3(PZP):c.903C>G (p.His301Gln)	KLRG1, PZP (H301Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3311909	NM_002864.3(PZP):c.886A>G (p.Ile296Val)	KLRG1, PZP (I296V)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2240948	NM_002864.3(PZP):c.859A>T (p.Ser287Cys)	KLRG1, PZP (S287C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3311908	NM_002864.3(PZP):c.771G>T (p.Lys257Asn)	KLRG1, PZP (K257N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3150288	NM_002864.3(PZP):c.737A>G (p.Asn246Ser)	KLRG1, PZP (N246S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2301804	NM_002864.3(PZP):c.724G>C (p.Asp242His)	KLRG1, PZP (D242H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3150286	NM_002864.3(PZP):c.722T>C (p.Met241Thr)	KLRG1, PZP (M241T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3150285	NM_002864.3(PZP):c.658G>A (p.Val220Met)	KLRG1, PZP (V220M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3150284	NM_002864.3(PZP):c.621G>C (p.Gln207His)	KLRG1, PZP (Q207H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2289539	NM_002864.3(PZP):c.485C>A (p.Pro162Gln)	KLRG1, PZP (P162Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2372561	NM_002864.3(PZP):c.437G>A (p.Arg146His)	KLRG1, PZP (R146H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3311911	NM_002864.3(PZP):c.223G>C (p.Asp75His)	KLRG1, PZP (D75H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3150271	NM_002864.3(PZP):c.212G>A (p.Ser71Asn)	KLRG1, PZP (S71N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3150265	NM_002864.3(PZP):c.128C>T (p.Pro43Leu)	KLRG1, PZP (P43L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3311910	NM_002864.3(PZP):c.86A>C (p.Gln29Pro)	KLRG1, PZP (Q29P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2532973	NM_002864.3(PZP):c.70A>G (p.Asn24Asp)	KLRG1, PZP (N24D)	Single nucleotide variant (missense variant)	not specified	GLikely benign

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Items: 72