ClinVar for Gene (Select 10219) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
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)	KLRG1, A2M (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
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 2559055	NM_000014.6(A2M):c.260T>A (p.Val87Asp)	A2M, KLRG1 (V87D)	Single nucleotide variant (missense variant +1 more)	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 2552688	NM_000014.6(A2M):c.98T>C (p.Val33Ala)	A2M, KLRG1 (V33A)	Single nucleotide variant (missense variant +1 more)	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 2540438	NM_002864.3(PZP):c.2983T>A (p.Tyr995Asn)	KLRG1, PZP (Y995N)	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
Select item 2531002	NM_000014.6(A2M):c.1214T>C (p.Val405Ala)	A2M, KLRG1 (V305A +2 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
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 2527543	NM_000014.6(A2M):c.2251G>C (p.Val751Leu)	A2M, KLRG1 (V601L +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2526714	NM_000014.6(A2M):c.1868C>G (p.Pro623Arg)	A2M, KLRG1 (P523R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2521978	NM_000014.6(A2M):c.3674C>T (p.Ser1225Leu)	A2M, KLRG1 (S1075L +2 more)	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 2515841	NM_000014.6(A2M):c.1205A>G (p.His402Arg)	A2M, KLRG1 (H252R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2514869	NM_000014.6(A2M):c.1735C>G (p.Pro579Ala)	A2M, KLRG1 (P429A +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2514675	NM_000014.6(A2M):c.622C>G (p.Gln208Glu)	A2M, KLRG1 (Q108E +2 more)	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 2494083	NM_000014.6(A2M):c.490C>G (p.Leu164Val)	A2M, KLRG1 (L14V +2 more)	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 2485953	NM_002864.3(PZP):c.2528C>T (p.Ser843Phe)	KLRG1, PZP (S843F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
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 2478090	NM_002864.3(PZP):c.2637T>A (p.Ser879Arg)	KLRG1, PZP (S879R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2476900	NM_000014.6(A2M):c.350G>T (p.Arg117Leu)	A2M, KLRG1 (R17L +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2474181	NM_000014.6(A2M):c.3385G>A (p.Glu1129Lys)	A2M, KLRG1 (E1129K +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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