KLRG1[gene] - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 619591	NC_000012.12:g.(1_3750000)_(5250000_9000000)del	GAPDH, GAU1 +477 more	Deletion	Tumoral calcinosis, hyperphosphatemic, familial, 1	Gnot provided
Select item 151004	GRCh38/hg38 12p13.33-11.1(chr12:54427-34608071)x4	TAS2R9, TEAD4 +1258 more	Copy number gain	See cases	GPathogenic
Select item 153962	GRCh38/hg38 12p13.33-11.1(chr12:64620-34682902)x4	CLEC12A, CLEC12A-AS1 +1258 more	Copy number gain	See cases	GPathogenic
Select item 59794	GRCh38/hg38 12p13.33-11.1(chr12:77187-34380176)x3	LOC126861410, LOC126861411 +1258 more	Copy number gain	See cases	GPathogenic
Select item 59795	GRCh38/hg38 12p13.33-12.1(chr12:80412-25470329)x3	A2M, A2M-AS1 +1009 more	Copy number gain	See cases	GPathogenic
Select item 147419	GRCh38/hg38 12p13.33-11.1(chr12:121255-34603274)x3	LOC130007230, LOC130007231 +1257 more	Copy number gain	See cases	GPathogenic
Select item 150740	GRCh38/hg38 12p13.33-q24.33(chr12:121271-133196807)x3	FERRY3, FGD4 +4837 more	Copy number gain	See cases	GPathogenic
Select item 150158	GRCh38/hg38 12p13.33-11.1(chr12:121271-34603261)x3	LOC126861494, LOC126861495 +1257 more	Copy number gain	See cases	GPathogenic
Select item 59799	GRCh38/hg38 12p13.33-11.1(chr12:212976-33926913)x4	CACNA1C-AS2, CACNA1C-AS4 +1242 more	Copy number gain	See cases	GPathogenic
Select item 153563	GRCh38/hg38 12p13.33-12.2(chr12:1258274-20657577)x3	A2M, A2M-AS1 +853 more	Copy number gain	See cases	GPathogenic
Select item 148626	GRCh38/hg38 12p13.33-12.3(chr12:2871741-14987348)x3	LOC130007190, LOC130007191 +698 more	Copy number gain	See cases	GPathogenic
Select item 152932	GRCh38/hg38 12p13.31(chr12:8839030-9134304)x3	A2M, A2M-AS1 +12 more	Copy number gain	See cases	GUncertain significance
Select item 2459065	NM_005810.4(KLRG1):c.74A>G (p.Gln25Arg)	KLRG1 (Q25R)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2269053	NM_005810.4(KLRG1):c.164T>C (p.Leu55Pro)	KLRG1 (L55P)	Single nucleotide variant (missense variant +2 more)	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 2279614	NM_005810.4(KLRG1):c.341C>T (p.Thr114Met)	KLRG1 (T35M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2204464	NM_005810.4(KLRG1):c.385G>A (p.Ala129Thr)	KLRG1 (A129T +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2204465	NM_005810.4(KLRG1):c.386C>A (p.Ala129Asp)	KLRG1 (A50D +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2337995	NM_005810.4(KLRG1):c.403C>A (p.Leu135Met)	KLRG1 (L135M +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2232537	NM_005810.4(KLRG1):c.556A>G (p.Lys186Glu)	KLRG1 (K107E +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 1279791	NM_005810.4(KLRG1):c.*1044A>G	KLRG1	Single nucleotide variant (3 prime UTR variant +1 more)	not provided	GBenign
Select item 2247316	NM_000014.6(A2M):c.4399T>G (p.Cys1467Gly)	A2M, KLRG1 (C1317G +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2205638	NM_000014.6(A2M):c.4364C>T (p.Thr1455Met)	A2M, KLRG1 (T1355M +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2265103	NM_000014.6(A2M):c.4264G>A (p.Val1422Met)	A2M, KLRG1 (V1322M +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 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 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 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 2303234	NM_000014.6(A2M):c.4066A>G (p.Lys1356Glu)	A2M, KLRG1 (K1206E +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2252771	NM_000014.6(A2M):c.4057G>C (p.Asp1353His)	A2M, KLRG1 (D1253H +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 2230211	NM_000014.6(A2M):c.3829C>A (p.Gln1277Lys)	A2M, KLRG1 (Q1127K +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 713107	NM_000014.6(A2M):c.3756+4G>A	A2M, KLRG1	Single nucleotide variant	not provided	GBenign
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 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 2268524	NM_000014.6(A2M):c.3593A>T (p.Glu1198Val)	A2M, KLRG1 (E1198V +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
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 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 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 781242	NM_000014.6(A2M):c.3456T>C (p.Tyr1152=)	A2M, KLRG1	Single nucleotide variant (synonymous variant)	not provided	GBenign
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
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 2332459	NM_000014.6(A2M):c.3299C>A (p.Thr1100Asn)	A2M, KLRG1 (T1000N +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
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 711716	NM_000014.6(A2M):c.3092G>A (p.Arg1031Gln)	A2M, KLRG1 (R881Q +2 more)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 726982	NM_000014.6(A2M):c.3084T>C (p.Phe1028=)	KLRG1, A2M	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2264696	NM_000014.6(A2M):c.3014T>C (p.Ile1005Thr)	A2M, KLRG1 (I1005T +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2376401	NM_000014.6(A2M):c.3008A>C (p.Lys1003Thr)	A2M, KLRG1 (K903T +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 18171	NM_000014.6(A2M):c.2998A>G (p.Ile1000Val)	A2M, KLRG1 (I1000V +2 more)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 2405095	NM_000014.6(A2M):c.2962G>A (p.Asp988Asn)	A2M, KLRG1 (D838N +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 18172	NM_000014.6(A2M):c.2915G>A (p.Cys972Tyr)	A2M, KLRG1 (C972Y +2 more)	Single nucleotide variant (missense variant)	ALPHA-2-MACROGLOBULIN POLYMORPHISM	GBenign
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 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 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 2237949	NM_000014.6(A2M):c.2785G>C (p.Glu929Gln)	A2M, KLRG1 (E779Q +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1049273	NM_000014.6(A2M):c.2771-115C>G	A2M, KLRG1	Single nucleotide variant (intron variant)	not provided	GUncertain significance
Select item 2277243	NM_000014.6(A2M):c.2689G>T (p.Asp897Tyr)	A2M, KLRG1 (D897Y +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
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 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 3060838	NM_000014.6(A2M):c.2597-4T>A	A2M, KLRG1	Single nucleotide variant (intron variant)	A2M-related disorder	GBenign
Select item 714506	NM_000014.6(A2M):c.2532G>A (p.Ala844=)	A2M, KLRG1	Single nucleotide variant (synonymous variant)	not provided	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 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 3041113	NM_000014.6(A2M):c.2439G>A (p.Thr813=)	A2M, KLRG1	Single nucleotide variant (synonymous variant)	A2M-related disorder	GLikely benign
Select item 2335320	NM_000014.6(A2M):c.2411G>A (p.Arg804His)	A2M, KLRG1 (R704H +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2288432	NM_000014.6(A2M):c.2390C>T (p.Thr797Ile)	A2M, KLRG1 (T697I +2 more)	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 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 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 974740	NC_000012.12:g.9092896_9155947dup	A2M, KLRG1	Duplication	Megacolon	GUncertain significance
Select item 18173	NM_000014.6(A2M):c.2125+1_2126-1del	A2M, KLRG1	Deletion (splice acceptor variant +1 more)	ALPHA-2-MACROGLOBULIN POLYMORPHISM	GBenign
Select item 402328	NM_000014.6(A2M):c.2126-6_2126-2del	A2M, KLRG1	Deletion (splice acceptor variant)	not specified +1 more	GBenign
Select item 18174	NM_000014.6(A2M):c.2111G>A (p.Arg704His)	A2M, KLRG1 (R704H +2 more)	Single nucleotide variant (missense variant)	ALPHA-2-MACROGLOBULIN POLYMORPHISM	GBenign
Select item 2233837	NM_000014.6(A2M):c.2039A>G (p.Asn680Ser)	A2M, KLRG1 (N580S +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 726983	NM_000014.6(A2M):c.2008C>T (p.Leu670=)	A2M, KLRG1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
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 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 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 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 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 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 2305175	NM_000014.6(A2M):c.1760T>C (p.Val587Ala)	A2M, KLRG1 (V487A +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
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 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 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 3057371	NM_000014.6(A2M):c.1644C>T (p.Thr548=)	A2M, KLRG1	Single nucleotide variant (synonymous variant)	A2M-related disorder	GLikely benign
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 3038794	NM_000014.6(A2M):c.1506G>A (p.Lys502=)	A2M, KLRG1	Single nucleotide variant (synonymous 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 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 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 2272879	NM_000014.6(A2M):c.1360C>T (p.Pro454Ser)	A2M, KLRG1 (P304S +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 768514	NM_000014.6(A2M):c.1311G>A (p.Val437=)	A2M, KLRG1	Single nucleotide variant (synonymous variant)	not provided	GBenign
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 3049620	NM_000014.6(A2M):c.1275C>T (p.Tyr425=)	A2M, KLRG1	Single nucleotide variant (synonymous variant)	A2M-related disorder	GBenign
Select item 2218210	NM_000014.6(A2M):c.1235C>T (p.Thr412Ile)	A2M, KLRG1 (T262I +2 more)	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

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