| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 1 | g.161544763C>A | CA1211385 | FCGR3A | c.515G>T (p.Cys172Phe) c.512G>T (p.Cys171Phe) c.464G>T (p.Cys155Phe) c.623G>T (p.Cys208Phe) c.565G>T c.620G>T (p.Cys207Phe) c.428-1564G>T (n.428-1564G>T) c.830G>T (p.Cys277Phe) c.827G>T (p.Cys276Phe) c.635-1564G>T (n.635-1564G>T) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 1 | g.161544763C= | CA1149151868 | FCGR3A | c.515G= (p.Cys172=) c.512G= (p.Cys171=) c.464G= (p.Cys155=) c.623G= (p.Cys208=) c.565G= c.620G= (p.Cys207=) c.428-1564G= (n.428-1564G=) c.830G= (p.Cys277=) c.827G= (p.Cys276=) c.635-1564G= (n.635-1564G=) | |
| 1 | g.161544763C>G | CA343367473 | FCGR3A | c.515G>C (p.Cys172Ser) c.512G>C (p.Cys171Ser) c.464G>C (p.Cys155Ser) c.623G>C (p.Cys208Ser) c.565G>C c.620G>C (p.Cys207Ser) c.428-1564G>C (n.428-1564G>C) c.830G>C (p.Cys277Ser) c.827G>C (p.Cys276Ser) c.635-1564G>C (n.635-1564G>C) | |
| 1 | g.161544763C>T | CA343367474 | FCGR3A | c.515G>A (p.Cys172Tyr) c.512G>A (p.Cys171Tyr) c.464G>A (p.Cys155Tyr) c.623G>A (p.Cys208Tyr) c.565G>A c.620G>A (p.Cys207Tyr) c.428-1564G>A (n.428-1564G>A) c.830G>A (p.Cys277Tyr) c.827G>A (p.Cys276Tyr) c.635-1564G>A (n.635-1564G>A) | dbSNP gnomAD v2 gnomAD v4 |
| 1 | g.161544764A= | CA1202785229 | FCGR3A | c.514T= (p.Cys172=) c.511T= (p.Cys171=) c.463T= (p.Cys155=) c.622T= (p.Cys208=) c.564T= c.619T= (p.Cys207=) c.428-1565T= (n.428-1565T=) c.829T= (p.Cys277=) c.826T= (p.Cys276=) c.635-1565T= (n.635-1565T=) | |
| 1 | g.161544764A>C | CA343367479 | FCGR3A | c.514T>G (p.Cys172Gly) c.511T>G (p.Cys171Gly) c.463T>G (p.Cys155Gly) c.622T>G (p.Cys208Gly) c.564T>G c.619T>G (p.Cys207Gly) c.428-1565T>G (n.428-1565T>G) c.829T>G (p.Cys277Gly) c.826T>G (p.Cys276Gly) c.635-1565T>G (n.635-1565T>G) | |
| 1 | g.161544764A>G | CA343367477 | FCGR3A | c.514T>C (p.Cys172Arg) c.511T>C (p.Cys171Arg) c.463T>C (p.Cys155Arg) c.622T>C (p.Cys208Arg) c.564T>C c.619T>C (p.Cys207Arg) c.428-1565T>C (n.428-1565T>C) c.829T>C (p.Cys277Arg) c.826T>C (p.Cys276Arg) c.635-1565T>C (n.635-1565T>C) | dbSNP COSMIC |
| 1 | g.161544764A>T | CA343367478 | FCGR3A | c.514T>A (p.Cys172Ser) c.511T>A (p.Cys171Ser) c.463T>A (p.Cys155Ser) c.622T>A (p.Cys208Ser) c.564T>A c.619T>A (p.Cys207Ser) c.428-1565T>A (n.428-1565T>A) c.829T>A (p.Cys277Ser) c.826T>A (p.Cys276Ser) c.635-1565T>A (n.635-1565T>A) | |
| 1 | g.161544765G>A | CA421612452 | FCGR3A | c.513C>T (p.Phe171=) c.510C>T (p.Phe170=) c.462C>T (p.Phe154=) c.621C>T (p.Phe207=) c.563C>T c.618C>T (p.Phe206=) c.428-1566C>T (n.428-1566C>T) c.828C>T (p.Phe276=) c.825C>T (p.Phe275=) c.635-1566C>T (n.635-1566C>T) | |
| 1 | g.161544765G>C | CA343367480 | FCGR3A | c.513C>G (p.Phe171Leu) c.510C>G (p.Phe170Leu) c.462C>G (p.Phe154Leu) c.621C>G (p.Phe207Leu) c.563C>G c.618C>G (p.Phe206Leu) c.428-1566C>G (n.428-1566C>G) c.828C>G (p.Phe276Leu) c.825C>G (p.Phe275Leu) c.635-1566C>G (n.635-1566C>G) | |
| 1 | g.161544765G>T | CA343367481 | FCGR3A | c.513C>A (p.Phe171Leu) c.510C>A (p.Phe170Leu) c.462C>A (p.Phe154Leu) c.621C>A (p.Phe207Leu) c.563C>A c.618C>A (p.Phe206Leu) c.428-1566C>A (n.428-1566C>A) c.828C>A (p.Phe276Leu) c.825C>A (p.Phe275Leu) c.635-1566C>A (n.635-1566C>A) | |
| 1 | g.161544766A>C | CA343367483 | FCGR3A | c.512T>G (p.Phe171Cys) c.509T>G (p.Phe170Cys) c.461T>G (p.Phe154Cys) c.620T>G (p.Phe207Cys) c.562T>G c.617T>G (p.Phe206Cys) c.428-1567T>G (n.428-1567T>G) c.827T>G (p.Phe276Cys) c.824T>G (p.Phe275Cys) c.635-1567T>G (n.635-1567T>G) | |
| 1 | g.161544766A>G | CA343367485 | FCGR3A | c.512T>C (p.Phe171Ser) c.509T>C (p.Phe170Ser) c.461T>C (p.Phe154Ser) c.620T>C (p.Phe207Ser) c.562T>C c.617T>C (p.Phe206Ser) c.428-1567T>C (n.428-1567T>C) c.827T>C (p.Phe276Ser) c.824T>C (p.Phe275Ser) c.635-1567T>C (n.635-1567T>C) | |
| 1 | g.161544766A>T | CA343367486 | FCGR3A | c.512T>A (p.Phe171Tyr) c.509T>A (p.Phe170Tyr) c.461T>A (p.Phe154Tyr) c.620T>A (p.Phe207Tyr) c.562T>A c.617T>A (p.Phe206Tyr) c.428-1567T>A (n.428-1567T>A) c.827T>A (p.Phe276Tyr) c.824T>A (p.Phe275Tyr) c.635-1567T>A (n.635-1567T>A) | |
| 1 | g.161544767A= | CA1202785230 | FCGR3A | c.511T= (p.Phe171=) c.508T= (p.Phe170=) c.460T= (p.Phe154=) c.619T= (p.Phe207=) c.561T= c.616T= (p.Phe206=) c.428-1568T= (n.428-1568T=) c.826T= (p.Phe276=) c.823T= (p.Phe275=) c.635-1568T= (n.635-1568T=) | |
| 1 | g.161544767A>C | CA343367488 | FCGR3A | c.511T>G (p.Phe171Val) c.508T>G (p.Phe170Val) c.460T>G (p.Phe154Val) c.619T>G (p.Phe207Val) c.561T>G c.616T>G (p.Phe206Val) c.428-1568T>G (n.428-1568T>G) c.826T>G (p.Phe276Val) c.823T>G (p.Phe275Val) c.635-1568T>G (n.635-1568T>G) | dbSNP gnomAD v2 gnomAD v4 |
| 1 | g.161544767A>G | CA343367489 | FCGR3A | c.511T>C (p.Phe171Leu) c.508T>C (p.Phe170Leu) c.460T>C (p.Phe154Leu) c.619T>C (p.Phe207Leu) c.561T>C c.616T>C (p.Phe206Leu) c.428-1568T>C (n.428-1568T>C) c.826T>C (p.Phe276Leu) c.823T>C (p.Phe275Leu) c.635-1568T>C (n.635-1568T>C) | |
| 1 | g.161544767A>T | CA1211386 | FCGR3A | c.511T>A (p.Phe171Ile) c.508T>A (p.Phe170Ile) c.460T>A (p.Phe154Ile) c.619T>A (p.Phe207Ile) c.561T>A c.616T>A (p.Phe206Ile) c.428-1568T>A (n.428-1568T>A) c.826T>A (p.Phe276Ile) c.823T>A (p.Phe275Ile) c.635-1568T>A (n.635-1568T>A) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 1 | g.161544768G>A | CA421612454 | FCGR3A | c.510C>T (p.Tyr170=) c.507C>T (p.Tyr169=) c.459C>T (p.Tyr153=) c.618C>T (p.Tyr206=) c.560C>T c.615C>T (p.Tyr205=) c.428-1569C>T (n.428-1569C>T) c.825C>T (p.Tyr275=) c.822C>T (p.Tyr274=) c.635-1569C>T (n.635-1569C>T) | |
| 1 | g.161544768G>C | CA343367491 | FCGR3A | c.510C>G (p.Tyr170Ter) c.507C>G (p.Tyr169Ter) c.459C>G (p.Tyr153Ter) c.618C>G (p.Tyr206Ter) c.560C>G c.615C>G (p.Tyr205Ter) c.428-1569C>G (n.428-1569C>G) c.825C>G (p.Tyr275Ter) c.822C>G (p.Tyr274Ter) c.635-1569C>G (n.635-1569C>G) | |
| 1 | g.161544768G>T | CA343367493 | FCGR3A | c.510C>A (p.Tyr170Ter) c.507C>A (p.Tyr169Ter) c.459C>A (p.Tyr153Ter) c.618C>A (p.Tyr206Ter) c.560C>A c.615C>A (p.Tyr205Ter) c.428-1569C>A (n.428-1569C>A) c.825C>A (p.Tyr275Ter) c.822C>A (p.Tyr274Ter) c.635-1569C>A (n.635-1569C>A) | |
| 1 | g.161544770_161544781del | CA2573939412 | FCGR3A | c.499_510del (p.Ser167_Tyr170del) c.496_507del (p.Ser166_Tyr169del) c.448_459del (p.Ser150_Tyr153del) c.607_618del (p.Ser203_Tyr206del) c.549_560del c.604_615del (p.Ser202_Tyr205del) c.428-1580_428-1569del (n.428-1580_428-1569del) c.814_825del (p.Ser272_Tyr275del) c.811_822del (p.Ser271_Tyr274del) c.635-1580_635-1569del (n.635-1580_635-1569del) | |
| 1 | g.161544769T>A | CA343367496 | FCGR3A | c.509A>T (p.Tyr170Phe) c.506A>T (p.Tyr169Phe) c.458A>T (p.Tyr153Phe) c.617A>T (p.Tyr206Phe) c.559A>T c.614A>T (p.Tyr205Phe) c.428-1570A>T (n.428-1570A>T) c.824A>T (p.Tyr275Phe) c.821A>T (p.Tyr274Phe) c.635-1570A>T (n.635-1570A>T) | |
| 1 | g.161544769T>C | CA1211387 | FCGR3A | c.509A>G (p.Tyr170Cys) c.506A>G (p.Tyr169Cys) c.458A>G (p.Tyr153Cys) c.617A>G (p.Tyr206Cys) c.559A>G c.614A>G (p.Tyr205Cys) c.428-1570A>G (n.428-1570A>G) c.824A>G (p.Tyr275Cys) c.821A>G (p.Tyr274Cys) c.635-1570A>G (n.635-1570A>G) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 1 | g.161544769T>G | CA343367494 | FCGR3A | c.509A>C (p.Tyr170Ser) c.506A>C (p.Tyr169Ser) c.458A>C (p.Tyr153Ser) c.617A>C (p.Tyr206Ser) c.559A>C c.614A>C (p.Tyr205Ser) c.428-1570A>C (n.428-1570A>C) c.824A>C (p.Tyr275Ser) c.821A>C (p.Tyr274Ser) c.635-1570A>C (n.635-1570A>C) | dbSNP gnomAD v2 gnomAD v4 |
| 1 | g.161544769T= | CA1147915952 | FCGR3A | c.509A= (p.Tyr170=) c.506A= (p.Tyr169=) c.458A= (p.Tyr153=) c.617A= (p.Tyr206=) c.559A= c.614A= (p.Tyr205=) c.428-1570A= (n.428-1570A=) c.824A= (p.Tyr275=) c.821A= (p.Tyr274=) c.635-1570A= (n.635-1570A=) | |
| 1 | g.161544770A= | CA1202785231 | FCGR3A | c.508T= (p.Tyr170=) c.505T= (p.Tyr169=) c.457T= (p.Tyr153=) c.616T= (p.Tyr206=) c.558T= c.613T= (p.Tyr205=) c.428-1571T= (n.428-1571T=) c.823T= (p.Tyr275=) c.820T= (p.Tyr274=) c.635-1571T= (n.635-1571T=) | |
| 1 | g.161544770A>C | CA31715354 | FCGR3A | c.508T>G (p.Tyr170Asp) c.505T>G (p.Tyr169Asp) c.457T>G (p.Tyr153Asp) c.616T>G (p.Tyr206Asp) c.558T>G c.613T>G (p.Tyr205Asp) c.428-1571T>G (n.428-1571T>G) c.823T>G (p.Tyr275Asp) c.820T>G (p.Tyr274Asp) c.635-1571T>G (n.635-1571T>G) | dbSNP |
| 1 | g.161544770A>G | CA343367498 | FCGR3A | c.508T>C (p.Tyr170His) c.505T>C (p.Tyr169His) c.457T>C (p.Tyr153His) c.616T>C (p.Tyr206His) c.558T>C c.613T>C (p.Tyr205His) c.428-1571T>C (n.428-1571T>C) c.823T>C (p.Tyr275His) c.820T>C (p.Tyr274His) c.635-1571T>C (n.635-1571T>C) | |
| 1 | g.161544770A>T | CA343367500 | FCGR3A | c.508T>A (p.Tyr170Asn) c.505T>A (p.Tyr169Asn) c.457T>A (p.Tyr153Asn) c.616T>A (p.Tyr206Asn) c.558T>A c.613T>A (p.Tyr205Asn) c.428-1571T>A (n.428-1571T>A) c.823T>A (p.Tyr275Asn) c.820T>A (p.Tyr274Asn) c.635-1571T>A (n.635-1571T>A) | |
| 1 | g.161544771G>A | CA421612455 | FCGR3A | c.507C>T (p.Ser169=) c.504C>T (p.Ser168=) c.456C>T (p.Ser152=) c.615C>T (p.Ser205=) c.557C>T c.612C>T (p.Ser204=) c.428-1572C>T (n.428-1572C>T) c.822C>T (p.Ser274=) c.819C>T (p.Ser273=) c.635-1572C>T (n.635-1572C>T) | gnomAD v4 |
| 1 | g.161544771G>C | CA421612456 | FCGR3A | c.507C>G (p.Ser169=) c.504C>G (p.Ser168=) c.456C>G (p.Ser152=) c.615C>G (p.Ser205=) c.557C>G c.612C>G (p.Ser204=) c.428-1572C>G (n.428-1572C>G) c.822C>G (p.Ser274=) c.819C>G (p.Ser273=) c.635-1572C>G (n.635-1572C>G) | |
| 1 | g.161544771G>T | CA421612457 | FCGR3A | c.507C>A (p.Ser169=) c.504C>A (p.Ser168=) c.456C>A (p.Ser152=) c.615C>A (p.Ser205=) c.557C>A c.612C>A (p.Ser204=) c.428-1572C>A (n.428-1572C>A) c.822C>A (p.Ser274=) c.819C>A (p.Ser273=) c.635-1572C>A (n.635-1572C>A) | |
| 1 | g.161544772G>A | CA1211388 | FCGR3A | c.506C>T (p.Ser169Phe) c.503C>T (p.Ser168Phe) c.455C>T (p.Ser152Phe) c.614C>T (p.Ser205Phe) c.556C>T c.611C>T (p.Ser204Phe) c.428-1573C>T (n.428-1573C>T) c.821C>T (p.Ser274Phe) c.818C>T (p.Ser273Phe) c.635-1573C>T (n.635-1573C>T) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 1 | g.161544772G>C | CA343367502 | FCGR3A | c.506C>G (p.Ser169Cys) c.503C>G (p.Ser168Cys) c.455C>G (p.Ser152Cys) c.614C>G (p.Ser205Cys) c.556C>G c.611C>G (p.Ser204Cys) c.428-1573C>G (n.428-1573C>G) c.821C>G (p.Ser274Cys) c.818C>G (p.Ser273Cys) c.635-1573C>G (n.635-1573C>G) | |
| 1 | g.161544772G= | CA1148898133 | FCGR3A | c.506C= (p.Ser169=) c.503C= (p.Ser168=) c.455C= (p.Ser152=) c.614C= (p.Ser205=) c.556C= c.611C= (p.Ser204=) c.428-1573C= (n.428-1573C=) c.821C= (p.Ser274=) c.818C= (p.Ser273=) c.635-1573C= (n.635-1573C=) | |
| 1 | g.161544772G>T | CA343367504 | FCGR3A | c.506C>A (p.Ser169Tyr) c.503C>A (p.Ser168Tyr) c.455C>A (p.Ser152Tyr) c.614C>A (p.Ser205Tyr) c.556C>A c.611C>A (p.Ser204Tyr) c.428-1573C>A (n.428-1573C>A) c.821C>A (p.Ser274Tyr) c.818C>A (p.Ser273Tyr) c.635-1573C>A (n.635-1573C>A) | |
| 1 | g.161544773A>C | CA343367507 | FCGR3A | c.505T>G (p.Ser169Ala) c.502T>G (p.Ser168Ala) c.454T>G (p.Ser152Ala) c.613T>G (p.Ser205Ala) c.555T>G c.610T>G (p.Ser204Ala) c.428-1574T>G (n.428-1574T>G) c.820T>G (p.Ser274Ala) c.817T>G (p.Ser273Ala) c.635-1574T>G (n.635-1574T>G) | |
| 1 | g.161544773A>G | CA343367508 | FCGR3A | c.505T>C (p.Ser169Pro) c.502T>C (p.Ser168Pro) c.454T>C (p.Ser152Pro) c.613T>C (p.Ser205Pro) c.555T>C c.610T>C (p.Ser204Pro) c.428-1574T>C (n.428-1574T>C) c.820T>C (p.Ser274Pro) c.817T>C (p.Ser273Pro) c.635-1574T>C (n.635-1574T>C) | |
| 1 | g.161544773A>T | CA343367509 | FCGR3A | c.505T>A (p.Ser169Thr) c.502T>A (p.Ser168Thr) c.454T>A (p.Ser152Thr) c.613T>A (p.Ser205Thr) c.555T>A c.610T>A (p.Ser204Thr) c.428-1574T>A (n.428-1574T>A) c.820T>A (p.Ser274Thr) c.817T>A (p.Ser273Thr) c.635-1574T>A (n.635-1574T>A) | |
| 1 | g.161544774G>A | CA421612461 | FCGR3A | c.504C>T (p.Gly168=) c.501C>T (p.Gly167=) c.453C>T (p.Gly151=) c.612C>T (p.Gly204=) c.554C>T c.609C>T (p.Gly203=) c.428-1575C>T (n.428-1575C>T) c.819C>T (p.Gly273=) c.816C>T (p.Gly272=) c.635-1575C>T (n.635-1575C>T) | dbSNP gnomAD v2 gnomAD v4 |
| 1 | g.161544774G>C | CA421612462 | FCGR3A | c.504C>G (p.Gly168=) c.501C>G (p.Gly167=) c.453C>G (p.Gly151=) c.612C>G (p.Gly204=) c.554C>G c.609C>G (p.Gly203=) c.428-1575C>G (n.428-1575C>G) c.819C>G (p.Gly273=) c.816C>G (p.Gly272=) c.635-1575C>G (n.635-1575C>G) | |
| 1 | g.161544774G= | CA1202785232 | FCGR3A | c.504C= (p.Gly168=) c.501C= (p.Gly167=) c.453C= (p.Gly151=) c.612C= (p.Gly204=) c.554C= c.609C= (p.Gly203=) c.428-1575C= (n.428-1575C=) c.819C= (p.Gly273=) c.816C= (p.Gly272=) c.635-1575C= (n.635-1575C=) | |
| 1 | g.161544774G>T | CA421612463 | FCGR3A | c.504C>A (p.Gly168=) c.501C>A (p.Gly167=) c.453C>A (p.Gly151=) c.612C>A (p.Gly204=) c.554C>A c.609C>A (p.Gly203=) c.428-1575C>A (n.428-1575C>A) c.819C>A (p.Gly273=) c.816C>A (p.Gly272=) c.635-1575C>A (n.635-1575C>A) | |
| 1 | g.161544775C>A | CA343367510 | FCGR3A | c.503G>T (p.Gly168Val) c.500G>T (p.Gly167Val) c.452G>T (p.Gly151Val) c.611G>T (p.Gly204Val) c.553G>T c.608G>T (p.Gly203Val) c.428-1576G>T (n.428-1576G>T) c.818G>T (p.Gly273Val) c.815G>T (p.Gly272Val) c.635-1576G>T (n.635-1576G>T) | gnomAD v4 |
| 1 | g.161544775C>G | CA343367511 | FCGR3A | c.503G>C (p.Gly168Ala) c.500G>C (p.Gly167Ala) c.452G>C (p.Gly151Ala) c.611G>C (p.Gly204Ala) c.553G>C c.608G>C (p.Gly203Ala) c.428-1576G>C (n.428-1576G>C) c.818G>C (p.Gly273Ala) c.815G>C (p.Gly272Ala) c.635-1576G>C (n.635-1576G>C) | |
| 1 | g.161544775C>T | CA343367512 | FCGR3A | c.503G>A (p.Gly168Asp) c.500G>A (p.Gly167Asp) c.452G>A (p.Gly151Asp) c.611G>A (p.Gly204Asp) c.553G>A c.608G>A (p.Gly203Asp) c.428-1576G>A (n.428-1576G>A) c.818G>A (p.Gly273Asp) c.815G>A (p.Gly272Asp) c.635-1576G>A (n.635-1576G>A) | COSMIC |
| 1 | g.161544776C>A | CA343367514 | FCGR3A | c.502G>T (p.Gly168Cys) c.499G>T (p.Gly167Cys) c.451G>T (p.Gly151Cys) c.610G>T (p.Gly204Cys) c.552G>T c.607G>T (p.Gly203Cys) c.428-1577G>T (n.428-1577G>T) c.817G>T (p.Gly273Cys) c.814G>T (p.Gly272Cys) c.635-1577G>T (n.635-1577G>T) | |
| 1 | g.161544776C= | CA1143392572 | FCGR3A | c.502G= (p.Gly168=) c.499G= (p.Gly167=) c.451G= (p.Gly151=) c.610G= (p.Gly204=) c.552G= c.607G= (p.Gly203=) c.428-1577G= (n.428-1577G=) c.817G= (p.Gly273=) c.814G= (p.Gly272=) c.635-1577G= (n.635-1577G=) | |
| 1 | g.161544776C>G | CA343367513 | FCGR3A | c.502G>C (p.Gly168Arg) c.499G>C (p.Gly167Arg) c.451G>C (p.Gly151Arg) c.610G>C (p.Gly204Arg) c.552G>C c.607G>C (p.Gly203Arg) c.428-1577G>C (n.428-1577G>C) c.817G>C (p.Gly273Arg) c.814G>C (p.Gly272Arg) c.635-1577G>C (n.635-1577G>C) |