ClinVar Miner

List of variants in gene PLA2G6 reported by CeGaT Center for Human Genetics Tuebingen

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Gene type:
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Total variants: 96
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HGVS dbSNP gnomAD frequency
NM_003560.4(PLA2G6):c.1743-137G>A rs55679135 0.00993
NM_003560.4(PLA2G6):c.1027G>A (p.Ala343Thr) rs11570680 0.00890
NM_003560.4(PLA2G6):c.2340C>T (p.Asn780=) rs138683183 0.00691
NM_003560.4(PLA2G6):c.425+464C>T rs11570633 0.00512
NM_003560.4(PLA2G6):c.187A>G (p.Arg63Gly) rs11570606 0.00379
NM_003560.4(PLA2G6):c.495G>C (p.Gly165=) rs150190277 0.00372
NM_003560.4(PLA2G6):c.972G>A (p.Ala324=) rs147755372 0.00249
NM_003560.4(PLA2G6):c.990C>T (p.Phe330=) rs146241431 0.00167
NM_003560.4(PLA2G6):c.1615G>A (p.Gly539Ser) rs143826762 0.00092
NM_003560.4(PLA2G6):c.1428-8C>T rs370288820 0.00058
NM_003560.4(PLA2G6):c.966C>T (p.His322=) rs144033740 0.00044
NM_003560.4(PLA2G6):c.2068G>A (p.Val690Ile) rs141777179 0.00041
NM_003560.4(PLA2G6):c.101C>T (p.Ser34Leu) rs147948449 0.00040
NM_003560.4(PLA2G6):c.416G>A (p.Arg139His) rs141825182 0.00038
NM_003560.4(PLA2G6):c.91G>A (p.Asp31Asn) rs150024227 0.00035
NM_003560.4(PLA2G6):c.1408A>G (p.Met470Val) rs201801144 0.00034
NM_003560.4(PLA2G6):c.1424G>A (p.Arg475Gln) rs139184008 0.00028
NM_003560.4(PLA2G6):c.2417C>G (p.Pro806Arg) rs140758033 0.00021
NM_003560.4(PLA2G6):c.396C>T (p.Arg132=) rs146252218 0.00018
NM_003560.4(PLA2G6):c.1427C>T (p.Thr476Ile) rs146684391 0.00017
NM_003560.4(PLA2G6):c.564C>T (p.Thr188=) rs185396488 0.00016
NM_003560.4(PLA2G6):c.2259C>T (p.Val753=) rs749966284 0.00014
NM_003560.4(PLA2G6):c.16C>T (p.Arg6Cys) rs143250889 0.00012
NM_003560.4(PLA2G6):c.1724C>T (p.Thr575Met) rs144012369 0.00011
NM_003560.4(PLA2G6):c.2277-6G>A rs370528124 0.00011
NM_003560.4(PLA2G6):c.447C>T (p.Asn149=) rs368631309 0.00011
NM_003560.4(PLA2G6):c.1725G>A (p.Thr575=) rs200599704 0.00010
NM_003560.4(PLA2G6):c.1268C>T (p.Ala423Val) rs199636953 0.00007
NM_003560.4(PLA2G6):c.1614C>T (p.Arg538=) rs373930150 0.00007
NM_003560.4(PLA2G6):c.2370T>G (p.Tyr790Ter) rs121908680 0.00006
NM_003560.4(PLA2G6):c.901C>T (p.Arg301Cys) rs367854265 0.00006
NM_003560.4(PLA2G6):c.2355C>T (p.Thr785=) rs146591896 0.00005
NM_003560.4(PLA2G6):c.1267G>A (p.Ala423Thr) rs746217497 0.00004
NM_003560.4(PLA2G6):c.898G>A (p.Ala300Thr) rs528966598 0.00004
NM_003560.4(PLA2G6):c.1548G>A (p.Ala516=) rs1031583350 0.00003
NM_003560.4(PLA2G6):c.1234G>A (p.Glu412Lys) rs575880571 0.00002
NM_003560.4(PLA2G6):c.1286C>T (p.Ala429Val) rs188895903 0.00002
NM_003560.4(PLA2G6):c.1779G>A (p.Pro593=) rs746984683 0.00002
NM_003560.4(PLA2G6):c.1894C>T (p.Arg632Trp) rs121908683 0.00002
NM_003560.4(PLA2G6):c.209G>A (p.Arg70Gln) rs11570607 0.00002
NM_003560.4(PLA2G6):c.2277-7C>T rs571223704 0.00002
NM_003560.4(PLA2G6):c.344G>A (p.Arg115His) rs138040351 0.00002
NM_003560.4(PLA2G6):c.803C>T (p.Ala268Val) rs762715738 0.00002
NM_003560.4(PLA2G6):c.858C>T (p.Tyr286=) rs756418076 0.00002
NM_003560.4(PLA2G6):c.948G>A (p.Ala316=) rs747199329 0.00002
NM_003560.4(PLA2G6):c.109C>T (p.Arg37Ter) rs200075782 0.00001
NM_003560.4(PLA2G6):c.1255C>T (p.His419Tyr) rs370873601 0.00001
NM_003560.4(PLA2G6):c.1414G>A (p.Asp472Asn) rs375874092 0.00001
NM_003560.4(PLA2G6):c.1423C>T (p.Arg475Trp) rs755845373 0.00001
NM_003560.4(PLA2G6):c.1531C>G (p.Leu511Val) rs886057503 0.00001
NM_003560.4(PLA2G6):c.1627C>T (p.Arg543Cys) rs753874848 0.00001
NM_003560.4(PLA2G6):c.1771C>T (p.Arg591Trp) rs1043378899 0.00001
NM_003560.4(PLA2G6):c.1898C>T (p.Ala633Val) rs201657455 0.00001
NM_003560.4(PLA2G6):c.2416C>T (p.Pro806Ser) rs745664459 0.00001
NM_003560.4(PLA2G6):c.624C>T (p.Asn208=) rs536593896 0.00001
NM_003560.4(PLA2G6):c.986G>A (p.Arg329His) rs587784363 0.00001
NM_003560.4(PLA2G6):c.1022C>A (p.Ala341Asp) rs1030529431
NM_003560.4(PLA2G6):c.1029G>A (p.Ala343=)
NM_003560.4(PLA2G6):c.102G>A (p.Ser34=)
NM_003560.4(PLA2G6):c.1037G>A (p.Arg346His)
NM_003560.4(PLA2G6):c.1059G>A (p.Pro353=)
NM_003560.4(PLA2G6):c.1186+1G>A rs761815070
NM_003560.4(PLA2G6):c.1186C>T (p.Leu396Phe) rs778423680
NM_003560.4(PLA2G6):c.1187-5A>G rs1175689296
NM_003560.4(PLA2G6):c.1200G>A (p.Lys400=) rs2145748343
NM_003560.4(PLA2G6):c.1367A>C (p.His456Pro) rs1265504715
NM_003560.4(PLA2G6):c.1512G>A (p.Ser504=)
NM_003560.4(PLA2G6):c.1527G>C (p.Lys509Asn) rs1602096719
NM_003560.4(PLA2G6):c.1547_1548dup (p.Gly517fs) rs1555988204
NM_003560.4(PLA2G6):c.1612C>A (p.Arg538Ser) rs370691849
NM_003560.4(PLA2G6):c.1628G>T (p.Arg543Leu) rs763937995
NM_003560.4(PLA2G6):c.1651G>A (p.Gly551Ser)
NM_003560.4(PLA2G6):c.1672G>C (p.Gly558Arg)
NM_003560.4(PLA2G6):c.1772G>A (p.Arg591Gln) rs776713955
NM_003560.4(PLA2G6):c.1826G>A (p.Arg609Gln)
NM_003560.4(PLA2G6):c.1890G>C (p.Val630=)
NM_003560.4(PLA2G6):c.1894C>A (p.Arg632=)
NM_003560.4(PLA2G6):c.2035-870C>A
NM_003560.4(PLA2G6):c.2035-926G>A
NM_003560.4(PLA2G6):c.2098C>T (p.Gln700Ter) rs587784346
NM_003560.4(PLA2G6):c.2251G>T (p.Glu751Ter) rs1296348337
NM_003560.4(PLA2G6):c.2349G>A (p.Trp783Ter) rs775386225
NM_003560.4(PLA2G6):c.2356G>C (p.Glu786Gln) rs778705470
NM_003560.4(PLA2G6):c.266C>A (p.Ser89Tyr) rs142715413
NM_003560.4(PLA2G6):c.266C>T (p.Ser89Phe) rs142715413
NM_003560.4(PLA2G6):c.29C>A (p.Thr10Asn) rs1323819447
NM_003560.4(PLA2G6):c.319del (p.Leu107fs) rs776376695
NM_003560.4(PLA2G6):c.348C>T (p.Asn116=)
NM_003560.4(PLA2G6):c.379G>A (p.Val127Met)
NM_003560.4(PLA2G6):c.464C>T (p.Pro155Leu) rs2145819254
NM_003560.4(PLA2G6):c.668C>T (p.Pro223Leu) rs776753796
NM_003560.4(PLA2G6):c.707T>G (p.Val236Gly) rs2145803603
NM_003560.4(PLA2G6):c.736T>C (p.Cys246Arg)
NM_003560.4(PLA2G6):c.755del (p.Asn252fs) rs587784361
NM_003560.4(PLA2G6):c.85G>A (p.Val29Met)
NM_003560.4(PLA2G6):c.991G>A (p.Asp331Asn) rs199935023

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