ClinVar for Gene (Select 10219) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3339138	NM_000014.6(A2M):c.1078C>T (p.Arg360Ter)	A2M, KLRG1 (R210* +2 more)	Single nucleotide variant (nonsense)	not specified	GUncertain significance
Select item 3327032	NM_000014.6(A2M):c.2809C>T (p.Pro937Ser)	A2M, KLRG1 (P837S +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3318187	NM_000014.6(A2M):c.479A>T (p.Glu160Val)	A2M, KLRG1 (E10V +2 more)	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 3311917	NM_002864.3(PZP):c.3164T>A (p.Phe1055Tyr)	KLRG1, PZP (F1055Y)	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 3311913	NM_002864.3(PZP):c.1608G>A (p.Met536Ile)	KLRG1, PZP (M536I)	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 3311911	NM_002864.3(PZP):c.223G>C (p.Asp75His)	KLRG1, PZP (D75H)	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 3311909	NM_002864.3(PZP):c.886A>G (p.Ile296Val)	KLRG1, PZP (I296V)	Single nucleotide variant (missense variant)	not specified	GLikely benign
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 3309792	NM_000014.6(A2M):c.703G>T (p.Val235Leu)	A2M, KLRG1 (V135L +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3266898	NM_000014.6(A2M):c.4232G>A (p.Ser1411Asn)	A2M, KLRG1 (S1411N +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3266038	NM_000014.6(A2M):c.733G>A (p.Glu245Lys)	A2M, KLRG1 (E95K +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3265170	NM_000014.6(A2M):c.1747G>A (p.Ala583Thr)	A2M, KLRG1 (A483T +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3264313	NM_000014.6(A2M):c.1771C>T (p.Pro591Ser)	A2M, KLRG1 (P491S +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3263422	NM_000014.6(A2M):c.1456A>T (p.Thr486Ser)	A2M, KLRG1 (T336S +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3262551	NM_000014.6(A2M):c.1946A>G (p.Tyr649Cys)	A2M, KLRG1 (Y499C +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3261780	NM_000014.6(A2M):c.3349A>C (p.Thr1117Pro)	A2M, KLRG1 (T1017P +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3261445	NM_000014.6(A2M):c.1225A>G (p.Ile409Val)	A2M, KLRG1 (I259V +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3260852	NM_000014.6(A2M):c.445G>A (p.Val149Ile)	A2M, KLRG1 (V149I +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3258116	NM_000014.6(A2M):c.1616G>A (p.Arg539Gln)	A2M, KLRG1 (R539Q +2 more)	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 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 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 3150280	NM_002864.3(PZP):c.3881C>T (p.Thr1294Ile)	KLRG1, PZP (T1294I)	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 3150277	NM_002864.3(PZP):c.3196G>A (p.Glu1066Lys)	KLRG1, PZP (E1066K)	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 3150273	NM_002864.3(PZP):c.2320G>A (p.Gly774Arg)	KLRG1, PZP (G774R)	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 3150271	NM_002864.3(PZP):c.212G>A (p.Ser71Asn)	KLRG1, PZP (S71N)	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 3150269	NM_002864.3(PZP):c.1820C>T (p.Ala607Val)	KLRG1, PZP (A607V)	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 3150267	NM_002864.3(PZP):c.1492A>C (p.Lys498Gln)	KLRG1, PZP (K498Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
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 3150265	NM_002864.3(PZP):c.128C>T (p.Pro43Leu)	KLRG1, PZP (P43L)	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 3146264	NM_000014.6(A2M):c.278A>T (p.Lys93Met)	A2M, KLRG1 (K93M)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3145039	NM_000014.6(A2M):c.2601T>G (p.Asn867Lys)	A2M, KLRG1 (N767K +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3144731	NM_000014.6(A2M):c.2491T>C (p.Ser831Pro)	A2M, KLRG1 (S681P +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3143593	NM_000014.6(A2M):c.2286C>G (p.Ile762Met)	A2M, KLRG1 (I662M +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3142903	NM_000014.6(A2M):c.214A>C (p.Ser72Arg)	A2M, KLRG1 (S72R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3142343	NM_000014.6(A2M):c.2003G>A (p.Ser668Asn)	A2M, KLRG1 (S518N +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3141435	NM_000014.6(A2M):c.1846T>C (p.Ser616Pro)	A2M, KLRG1 (S616P +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3141194	NM_000014.6(A2M):c.1844C>T (p.Ala615Val)	A2M, KLRG1 (A515V +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3140339	NM_000014.6(A2M):c.1402C>A (p.Leu468Ile)	A2M, KLRG1 (L368I +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3140033	NM_000014.6(A2M):c.1373T>G (p.Phe458Cys)	A2M, KLRG1 (F458C +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3137445	NM_000014.6(A2M):c.1096T>C (p.Phe366Leu)	A2M, KLRG1 (F216L +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3115937	NM_005810.4(KLRG1):c.233G>A (p.Arg78His)	KLRG1 (R78H)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 3082359	NM_000014.6(A2M):c.616G>T (p.Val206Leu)	A2M, KLRG1 (V206L +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3080278	NM_000014.6(A2M):c.4205C>G (p.Ser1402Cys)	A2M, KLRG1 (S1252C +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3079719	NM_000014.6(A2M):c.4118G>A (p.Arg1373His)	A2M, KLRG1 (R1373H +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3078885	NM_000014.6(A2M):c.4033G>A (p.Val1345Met)	A2M, KLRG1 (V1345M +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3078057	NM_000014.6(A2M):c.3656C>A (p.Ala1219Asp)	A2M, KLRG1 (A1119D +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3077670	NM_000014.6(A2M):c.3653C>T (p.Thr1218Met)	A2M, KLRG1 (T1118M +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3076781	NM_000014.6(A2M):c.3488G>C (p.Arg1163Thr)	A2M, KLRG1 (R1013T +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3063250	GRCh37/hg19 12p13.33-11.1(chr12:173786-34835641)x3	A2M, A2ML1 +278 more	Copy number gain	not specified	GPathogenic
Select item 3060838	NM_000014.6(A2M):c.2597-4T>A	A2M, KLRG1	Single nucleotide variant (intron variant)	A2M-related disorder	GBenign
Select item 3058150	NM_000014.6(A2M):c.3494A>G (p.Glu1165Gly)	A2M, KLRG1 (E1015G +2 more)	Single nucleotide variant (missense variant)	A2M-related disorder	GLikely benign
Select item 3057371	NM_000014.6(A2M):c.1644C>T (p.Thr548=)	A2M, KLRG1	Single nucleotide variant (synonymous variant)	A2M-related disorder	GLikely benign
Select item 3057128	NM_000014.6(A2M):c.3277-9T>G	A2M, KLRG1	Single nucleotide variant (intron variant)	A2M-related disorder	GLikely benign
Select item 3057071	NM_000014.6(A2M):c.1296C>T (p.Tyr432=)	A2M, KLRG1	Single nucleotide variant (synonymous variant)	A2M-related disorder	GBenign
Select item 3052428	NM_000014.6(A2M):c.2679C>T (p.His893=)	A2M, KLRG1	Single nucleotide variant (synonymous variant)	A2M-related disorder	GLikely benign
Select item 3049620	NM_000014.6(A2M):c.1275C>T (p.Tyr425=)	A2M, KLRG1	Single nucleotide variant (synonymous variant)	A2M-related disorder	GBenign
Select item 3048942	NM_000014.6(A2M):c.2812A>G (p.Asn938Asp)	A2M, KLRG1 (N788D +2 more)	Single nucleotide variant (missense variant)	A2M-related disorder	GLikely benign
Select item 3046130	NM_000014.6(A2M):c.3485A>G (p.Lys1162Arg)	A2M, KLRG1 (K1012R +2 more)	Single nucleotide variant (missense variant)	A2M-related disorder	GLikely benign
Select item 3044172	NM_000014.6(A2M):c.1129G>A (p.Val377Ile)	A2M, KLRG1 (V227I +2 more)	Single nucleotide variant (missense variant)	A2M-related disorder	GBenign
Select item 3042128	NM_000014.6(A2M):c.2531C>T (p.Ala844Val)	A2M, KLRG1 (A694V +2 more)	Single nucleotide variant (missense variant)	A2M-related disorder	GBenign
Select item 3041387	NM_000014.6(A2M):c.53T>G (p.Leu18Arg)	A2M, KLRG1 (L18R)	Single nucleotide variant (missense variant +1 more)	A2M-related disorder	GLikely benign
Select item 3041113	NM_000014.6(A2M):c.2439G>A (p.Thr813=)	A2M, KLRG1	Single nucleotide variant (synonymous variant)	A2M-related disorder	GLikely benign
Select item 3038794	NM_000014.6(A2M):c.1506G>A (p.Lys502=)	A2M, KLRG1	Single nucleotide variant (synonymous variant)	A2M-related disorder	GLikely benign
Select item 3034349	NM_000014.6(A2M):c.1757G>A (p.Arg586Gln)	A2M, KLRG1 (R436Q +2 more)	Single nucleotide variant (missense variant)	A2M-related disorder	GLikely benign
Select item 3033677	NM_000014.6(A2M):c.1495-10T>C	A2M, KLRG1	Single nucleotide variant (intron variant)	A2M-related disorder	GLikely benign
Select item 2671607	Single allele	FGD4, FGF23 +278 more	Duplication	not provided	GPathogenic
Select item 2642695	NM_002864.3(PZP):c.234G>A (p.Ala78=)	KLRG1, PZP	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2642694	NM_002864.3(PZP):c.342G>A (p.Arg114=)	KLRG1, PZP	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2642693	NM_002864.3(PZP):c.1503C>T (p.Ile501=)	KLRG1, PZP	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2642692	NM_002864.3(PZP):c.3435C>T (p.Thr1145=)	KLRG1, PZP	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2620624	NM_000014.6(A2M):c.4204T>G (p.Ser1402Ala)	A2M, KLRG1 (S1252A +2 more)	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 2611046	NM_000014.6(A2M):c.1231A>G (p.Thr411Ala)	A2M, KLRG1 (T261A +2 more)	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 2610594	NM_002864.3(PZP):c.3646T>A (p.Ser1216Thr)	KLRG1, PZP (S1216T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2609731	NM_000014.6(A2M):c.2330G>A (p.Gly777Glu)	A2M, KLRG1 (G677E +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
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 2604162	NM_000014.6(A2M):c.2842G>T (p.Val948Phe)	A2M, KLRG1 (V798F +2 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2595488	NM_002864.3(PZP):c.2429G>A (p.Arg810His)	KLRG1, PZP (R810H)	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 2565704	NM_002864.3(PZP):c.1337G>A (p.Arg446His)	KLRG1, PZP (R446H)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2563952	NM_000014.6(A2M):c.1934G>A (p.Arg645His)	A2M, KLRG1 (R645H +2 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign

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