Chr Mutation (hg38) CAid Gene Transcript Linkouts
1g.161544760dupCA527135442FCGR3Ac.522dup (p.Leu175AlafsTer5)
c.519dup (p.Leu174AlafsTer5)
c.471dup (p.Leu158AlafsTer5)
c.630dup (p.Leu211AlafsTer5)
c.572dup
c.627dup (p.Leu210AlafsTer5)
c.428-1557dup (n.428-1557dup)
c.837dup (p.Leu280AlafsTer5)
c.834dup (p.Leu279AlafsTer5)
c.635-1557dup (n.635-1557dup)
dbSNP gnomAD v2 gnomAD v4
1g.161544760delCA2648790075FCGR3Ac.522del (p.Leu175PhefsTer12)
c.519del (p.Leu174PhefsTer12)
c.471del (p.Leu158PhefsTer12)
c.630del (p.Leu211PhefsTer12)
c.572del
c.627del (p.Leu210PhefsTer12)
c.428-1557del (n.428-1557del)
c.837del (p.Leu280PhefsTer12)
c.834del (p.Leu279PhefsTer12)
c.635-1557del (n.635-1557del)
gnomAD v4
1g.161544760C>ACA343367458FCGR3Ac.518G>T (p.Arg173Met)
c.515G>T (p.Arg172Met)
c.467G>T (p.Arg156Met)
c.626G>T (p.Arg209Met)
c.568G>T
c.623G>T (p.Arg208Met)
c.428-1561G>T (n.428-1561G>T)
c.833G>T (p.Arg278Met)
c.830G>T (p.Arg277Met)
c.635-1561G>T (n.635-1561G>T)
1g.161544760C>GCA343367459FCGR3Ac.518G>C (p.Arg173Thr)
c.515G>C (p.Arg172Thr)
c.467G>C (p.Arg156Thr)
c.626G>C (p.Arg209Thr)
c.568G>C
c.623G>C (p.Arg208Thr)
c.428-1561G>C (n.428-1561G>C)
c.833G>C (p.Arg278Thr)
c.830G>C (p.Arg277Thr)
c.635-1561G>C (n.635-1561G>C)
1g.161544760C>TCA343367460FCGR3Ac.518G>A (p.Arg173Lys)
c.515G>A (p.Arg172Lys)
c.467G>A (p.Arg156Lys)
c.626G>A (p.Arg209Lys)
c.568G>A
c.623G>A (p.Arg208Lys)
c.428-1561G>A (n.428-1561G>A)
c.833G>A (p.Arg278Lys)
c.830G>A (p.Arg277Lys)
c.635-1561G>A (n.635-1561G>A)
gnomAD v4
1g.161544760_161544761delinsCTCA1202785226FCGR3Ac.517_518delinsAG (p.Arg173=)
c.514_515delinsAG (p.Arg172=)
c.466_467delinsAG (p.Arg156=)
c.625_626delinsAG (p.Arg209=)
c.567_568delinsAG
c.622_623delinsAG (p.Arg208=)
c.428-1562_428-1561delinsAG (n.428-1562_428-1561delinsAG)
c.832_833delinsAG (p.Arg278=)
c.829_830delinsAG (p.Arg277=)
c.635-1562_635-1561delinsAG (n.635-1562_635-1561delinsAG)
1g.161544761delCA1211383FCGR3Ac.517del (p.Arg173GlyfsTer14)
c.514del (p.Arg172GlyfsTer14)
c.466del (p.Arg156GlyfsTer14)
c.625del (p.Arg209GlyfsTer14)
c.567del
c.622del (p.Arg208GlyfsTer14)
c.428-1562del (n.428-1562del)
c.832del (p.Arg278GlyfsTer14)
c.829del (p.Arg277GlyfsTer14)
c.635-1562del (n.635-1562del)
dbSNP ExAC gnomAD v2 gnomAD v4
1g.161544761T>ACA343367462FCGR3Ac.517A>T (p.Arg173Trp)
c.514A>T (p.Arg172Trp)
c.466A>T (p.Arg156Trp)
c.625A>T (p.Arg209Trp)
c.567A>T
c.622A>T (p.Arg208Trp)
c.428-1562A>T (n.428-1562A>T)
c.832A>T (p.Arg278Trp)
c.829A>T (p.Arg277Trp)
c.635-1562A>T (n.635-1562A>T)
dbSNP gnomAD v3 gnomAD v4
1g.161544761T>CCA343367464FCGR3Ac.517A>G (p.Arg173Gly)
c.514A>G (p.Arg172Gly)
c.466A>G (p.Arg156Gly)
c.625A>G (p.Arg209Gly)
c.567A>G
c.622A>G (p.Arg208Gly)
c.428-1562A>G (n.428-1562A>G)
c.832A>G (p.Arg278Gly)
c.829A>G (p.Arg277Gly)
c.635-1562A>G (n.635-1562A>G)
1g.161544761T>GCA421612448FCGR3Ac.517A>C (p.Arg173=)
c.514A>C (p.Arg172=)
c.466A>C (p.Arg156=)
c.625A>C (p.Arg209=)
c.567A>C
c.622A>C (p.Arg208=)
c.428-1562A>C (n.428-1562A>C)
c.832A>C (p.Arg278=)
c.829A>C (p.Arg277=)
c.635-1562A>C (n.635-1562A>C)
1g.161544761T=CA1202785227FCGR3Ac.517A= (p.Arg173=)
c.514A= (p.Arg172=)
c.466A= (p.Arg156=)
c.625A= (p.Arg209=)
c.567A=
c.622A= (p.Arg208=)
c.428-1562A= (n.428-1562A=)
c.832A= (p.Arg278=)
c.829A= (p.Arg277=)
c.635-1562A= (n.635-1562A=)
1g.161544762G>ACA1211384FCGR3Ac.516C>T (p.Cys172=)
c.513C>T (p.Cys171=)
c.465C>T (p.Cys155=)
c.624C>T (p.Cys208=)
c.566C>T
c.621C>T (p.Cys207=)
c.428-1563C>T (n.428-1563C>T)
c.831C>T (p.Cys277=)
c.828C>T (p.Cys276=)
c.635-1563C>T (n.635-1563C>T)
dbSNP ExAC gnomAD v2 gnomAD v4
1g.161544762G>CCA343367468FCGR3Ac.516C>G (p.Cys172Trp)
c.513C>G (p.Cys171Trp)
c.465C>G (p.Cys155Trp)
c.624C>G (p.Cys208Trp)
c.566C>G
c.621C>G (p.Cys207Trp)
c.428-1563C>G (n.428-1563C>G)
c.831C>G (p.Cys277Trp)
c.828C>G (p.Cys276Trp)
c.635-1563C>G (n.635-1563C>G)
1g.161544762G=CA1202785228FCGR3Ac.516C= (p.Cys172=)
c.513C= (p.Cys171=)
c.465C= (p.Cys155=)
c.624C= (p.Cys208=)
c.566C=
c.621C= (p.Cys207=)
c.428-1563C= (n.428-1563C=)
c.831C= (p.Cys277=)
c.828C= (p.Cys276=)
c.635-1563C= (n.635-1563C=)
1g.161544762G>TCA343367470FCGR3Ac.516C>A (p.Cys172Ter)
c.513C>A (p.Cys171Ter)
c.465C>A (p.Cys155Ter)
c.624C>A (p.Cys208Ter)
c.566C>A
c.621C>A (p.Cys207Ter)
c.428-1563C>A (n.428-1563C>A)
c.831C>A (p.Cys277Ter)
c.828C>A (p.Cys276Ter)
c.635-1563C>A (n.635-1563C>A)
gnomAD v4
1g.161544763C>ACA1211385FCGR3Ac.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
1g.161544763C=CA1149151868FCGR3Ac.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=)
1g.161544763C>GCA343367473FCGR3Ac.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)
1g.161544763C>TCA343367474FCGR3Ac.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
1g.161544764A=CA1202785229FCGR3Ac.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=)
1g.161544764A>CCA343367479FCGR3Ac.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)
1g.161544764A>GCA343367477FCGR3Ac.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
1g.161544764A>TCA343367478FCGR3Ac.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)
1g.161544765G>ACA421612452FCGR3Ac.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)
1g.161544765G>CCA343367480FCGR3Ac.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)
1g.161544765G>TCA343367481FCGR3Ac.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)
1g.161544766A>CCA343367483FCGR3Ac.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)
1g.161544766A>GCA343367485FCGR3Ac.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)
1g.161544766A>TCA343367486FCGR3Ac.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)
1g.161544767A=CA1202785230FCGR3Ac.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=)
1g.161544767A>CCA343367488FCGR3Ac.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
1g.161544767A>GCA343367489FCGR3Ac.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)
1g.161544767A>TCA1211386FCGR3Ac.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
1g.161544768G>ACA421612454FCGR3Ac.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)
1g.161544768G>CCA343367491FCGR3Ac.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)
1g.161544768G>TCA343367493FCGR3Ac.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)
1g.161544770_161544781delCA2573939412FCGR3Ac.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)
1g.161544769T>ACA343367496FCGR3Ac.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)
1g.161544769T>CCA1211387FCGR3Ac.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
1g.161544769T>GCA343367494FCGR3Ac.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
1g.161544769T=CA1147915952FCGR3Ac.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=)
1g.161544770A=CA1202785231FCGR3Ac.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=)
1g.161544770A>CCA31715354FCGR3Ac.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
1g.161544770A>GCA343367498FCGR3Ac.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)
1g.161544770A>TCA343367500FCGR3Ac.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)
1g.161544771G>ACA421612455FCGR3Ac.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
1g.161544771G>CCA421612456FCGR3Ac.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)
1g.161544771G>TCA421612457FCGR3Ac.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)
1g.161544772G>ACA1211388FCGR3Ac.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
1g.161544772G>CCA343367502FCGR3Ac.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)

Number of alleles fetched