Chr Mutation (hg38) CAid Gene Transcript Linkouts
1g.161544752A=CA1139793706FCGR3Ac.523T= (p.Phe175=)
c.526T= (p.Phe176=)
c.634T= (p.Phe212=)
n.576T=
c.631T= (p.Phe211=)
c.428-1553T= (n.428-1553T=)
c.841T= (p.Phe281=)
c.838T= (p.Phe280=)
c.635-1553T= (n.635-1553T=)
1g.161544752A>CCA1211378FCGR3Ac.523T>G (p.Phe175Val)
c.526T>G (p.Phe176Val)
c.634T>G (p.Phe212Val)
n.576T>G
c.631T>G (p.Phe211Val)
c.428-1553T>G (n.428-1553T>G)
c.841T>G (p.Phe281Val)
c.838T>G (p.Phe280Val)
c.635-1553T>G (n.635-1553T>G)
ClinVar dbSNP ExAC gnomAD
1g.161544752A>GCA1211379FCGR3Ac.523T>C (p.Phe175Leu)
c.526T>C (p.Phe176Leu)
c.634T>C (p.Phe212Leu)
n.576T>C
c.631T>C (p.Phe211Leu)
c.428-1553T>C (n.428-1553T>C)
c.841T>C (p.Phe281Leu)
c.838T>C (p.Phe280Leu)
c.635-1553T>C (n.635-1553T>C)
dbSNP ExAC gnomAD
1g.161544752A>TCA343367436FCGR3Ac.523T>A (p.Phe175Ile)
c.526T>A (p.Phe176Ile)
c.634T>A (p.Phe212Ile)
n.576T>A
c.631T>A (p.Phe211Ile)
c.428-1553T>A (n.428-1553T>A)
c.841T>A (p.Phe281Ile)
c.838T>A (p.Phe280Ile)
c.635-1553T>A (n.635-1553T>A)
1g.161544753A>CCA421612439FCGR3Ac.522T>G (p.Leu174=)
c.525T>G (p.Leu175=)
c.633T>G (p.Leu211=)
n.575T>G
c.630T>G (p.Leu210=)
c.428-1554T>G (n.428-1554T>G)
c.840T>G (p.Leu280=)
c.837T>G (p.Leu279=)
c.635-1554T>G (n.635-1554T>G)
1g.161544753A>GCA421612440FCGR3Ac.522T>C (p.Leu174=)
c.525T>C (p.Leu175=)
c.633T>C (p.Leu211=)
n.575T>C
c.630T>C (p.Leu210=)
c.428-1554T>C (n.428-1554T>C)
c.840T>C (p.Leu280=)
c.837T>C (p.Leu279=)
c.635-1554T>C (n.635-1554T>C)
1g.161544753A>TCA421612441FCGR3Ac.522T>A (p.Leu174=)
c.525T>A (p.Leu175=)
c.633T>A (p.Leu211=)
n.575T>A
c.630T>A (p.Leu210=)
c.428-1554T>A (n.428-1554T>A)
c.840T>A (p.Leu280=)
c.837T>A (p.Leu279=)
c.635-1554T>A (n.635-1554T>A)
1g.161544754A>CCA343367438FCGR3Ac.521T>G (p.Leu174Arg)
c.524T>G (p.Leu175Arg)
c.632T>G (p.Leu211Arg)
n.574T>G
c.629T>G (p.Leu210Arg)
c.428-1555T>G (n.428-1555T>G)
c.839T>G (p.Leu280Arg)
c.836T>G (p.Leu279Arg)
c.635-1555T>G (n.635-1555T>G)
1g.161544754A>GCA343367440FCGR3Ac.521T>C (p.Leu174Pro)
c.524T>C (p.Leu175Pro)
c.632T>C (p.Leu211Pro)
n.574T>C
c.629T>C (p.Leu210Pro)
c.428-1555T>C (n.428-1555T>C)
c.839T>C (p.Leu280Pro)
c.836T>C (p.Leu279Pro)
c.635-1555T>C (n.635-1555T>C)
1g.161544754A>TCA343367442FCGR3Ac.521T>A (p.Leu174His)
c.524T>A (p.Leu175His)
c.632T>A (p.Leu211His)
n.574T>A
c.629T>A (p.Leu210His)
c.428-1555T>A (n.428-1555T>A)
c.839T>A (p.Leu280His)
c.836T>A (p.Leu279His)
c.635-1555T>A (n.635-1555T>A)
1g.161544755G>ACA343367443FCGR3Ac.520C>T (p.Leu174Phe)
c.523C>T (p.Leu175Phe)
c.631C>T (p.Leu211Phe)
n.573C>T
c.628C>T (p.Leu210Phe)
c.428-1556C>T (n.428-1556C>T)
c.838C>T (p.Leu280Phe)
c.835C>T (p.Leu279Phe)
c.635-1556C>T (n.635-1556C>T)
1g.161544755G>CCA343367444FCGR3Ac.520C>G (p.Leu174Val)
c.523C>G (p.Leu175Val)
c.631C>G (p.Leu211Val)
n.573C>G
c.628C>G (p.Leu210Val)
c.428-1556C>G (n.428-1556C>G)
c.838C>G (p.Leu280Val)
c.835C>G (p.Leu279Val)
c.635-1556C>G (n.635-1556C>G)
1g.161544755G=CA1202785223FCGR3Ac.520C= (p.Leu174=)
c.523C= (p.Leu175=)
c.631C= (p.Leu211=)
n.573C=
c.628C= (p.Leu210=)
c.428-1556C= (n.428-1556C=)
c.838C= (p.Leu280=)
c.835C= (p.Leu279=)
c.635-1556C= (n.635-1556C=)
1g.161544755G>TCA343367445FCGR3Ac.520C>A (p.Leu174Ile)
c.523C>A (p.Leu175Ile)
c.631C>A (p.Leu211Ile)
n.573C>A
c.628C>A (p.Leu210Ile)
c.428-1556C>A (n.428-1556C>A)
c.838C>A (p.Leu280Ile)
c.835C>A (p.Leu279Ile)
c.635-1556C>A (n.635-1556C>A)
1g.161544756C>ACA421612442FCGR3Ac.519G>T (p.Gly173=)
c.522G>T (p.Gly174=)
c.630G>T (p.Gly210=)
n.572G>T
c.627G>T (p.Gly209=)
c.428-1557G>T (n.428-1557G>T)
c.837G>T (p.Gly279=)
c.834G>T (p.Gly278=)
c.635-1557G>T (n.635-1557G>T)
1g.161544756C>GCA421612443FCGR3Ac.519G>C (p.Gly173=)
c.522G>C (p.Gly174=)
c.630G>C (p.Gly210=)
n.572G>C
c.627G>C (p.Gly209=)
c.428-1557G>C (n.428-1557G>C)
c.837G>C (p.Gly279=)
c.834G>C (p.Gly278=)
c.635-1557G>C (n.635-1557G>C)
1g.161544756C>TCA421612445FCGR3Ac.519G>A (p.Gly173=)
c.522G>A (p.Gly174=)
c.630G>A (p.Gly210=)
n.572G>A
c.627G>A (p.Gly209=)
c.428-1557G>A (n.428-1557G>A)
c.837G>A (p.Gly279=)
c.834G>A (p.Gly278=)
c.635-1557G>A (n.635-1557G>A)
COSMIC
1g.161544760dupCA527135442FCGR3Ac.519dup (p.Leu174AlafsTer5)
c.522dup (p.Leu175AlafsTer5)
c.630dup (p.Leu211AlafsTer5)
n.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
1g.161544757C>ACA343367450FCGR3Ac.518G>T (p.Gly173Val)
c.521G>T (p.Gly174Val)
c.629G>T (p.Gly210Val)
n.571G>T
c.626G>T (p.Gly209Val)
c.428-1558G>T (n.428-1558G>T)
c.836G>T (p.Gly279Val)
c.833G>T (p.Gly278Val)
c.635-1558G>T (n.635-1558G>T)
1g.161544757C=CA1202785224FCGR3Ac.518G= (p.Gly173=)
c.521G= (p.Gly174=)
c.629G= (p.Gly210=)
n.571G=
c.626G= (p.Gly209=)
c.428-1558G= (n.428-1558G=)
c.836G= (p.Gly279=)
c.833G= (p.Gly278=)
c.635-1558G= (n.635-1558G=)
1g.161544757C>GCA343367448FCGR3Ac.518G>C (p.Gly173Ala)
c.521G>C (p.Gly174Ala)
c.629G>C (p.Gly210Ala)
n.571G>C
c.626G>C (p.Gly209Ala)
c.428-1558G>C (n.428-1558G>C)
c.836G>C (p.Gly279Ala)
c.833G>C (p.Gly278Ala)
c.635-1558G>C (n.635-1558G>C)
1g.161544757C>TCA1211380FCGR3Ac.518G>A (p.Gly173Glu)
c.521G>A (p.Gly174Glu)
c.629G>A (p.Gly210Glu)
n.571G>A
c.626G>A (p.Gly209Glu)
c.428-1558G>A (n.428-1558G>A)
c.836G>A (p.Gly279Glu)
c.833G>A (p.Gly278Glu)
c.635-1558G>A (n.635-1558G>A)
dbSNP ExAC gnomAD
1g.161544758C>ACA343367452FCGR3Ac.517G>T (p.Gly173Trp)
c.520G>T (p.Gly174Trp)
c.628G>T (p.Gly210Trp)
n.570G>T
c.625G>T (p.Gly209Trp)
c.428-1559G>T (n.428-1559G>T)
c.835G>T (p.Gly279Trp)
c.832G>T (p.Gly278Trp)
c.635-1559G>T (n.635-1559G>T)
1g.161544758C>GCA343367455FCGR3Ac.517G>C (p.Gly173Arg)
c.520G>C (p.Gly174Arg)
c.628G>C (p.Gly210Arg)
n.570G>C
c.625G>C (p.Gly209Arg)
c.428-1559G>C (n.428-1559G>C)
c.835G>C (p.Gly279Arg)
c.832G>C (p.Gly278Arg)
c.635-1559G>C (n.635-1559G>C)
1g.161544758C>TCA343367453FCGR3Ac.517G>A (p.Gly173Arg)
c.520G>A (p.Gly174Arg)
c.628G>A (p.Gly210Arg)
n.570G>A
c.625G>A (p.Gly209Arg)
c.428-1559G>A (n.428-1559G>A)
c.835G>A (p.Gly279Arg)
c.832G>A (p.Gly278Arg)
c.635-1559G>A (n.635-1559G>A)
1g.161544759C>ACA343367456FCGR3Ac.516G>T (p.Arg172Ser)
c.519G>T (p.Arg173Ser)
c.627G>T (p.Arg209Ser)
n.569G>T
c.624G>T (p.Arg208Ser)
c.428-1560G>T (n.428-1560G>T)
c.834G>T (p.Arg278Ser)
c.831G>T (p.Arg277Ser)
c.635-1560G>T (n.635-1560G>T)
1g.161544759C=CA1202785225FCGR3Ac.516G= (p.Arg172=)
c.519G= (p.Arg173=)
c.627G= (p.Arg209=)
n.569G=
c.624G= (p.Arg208=)
c.428-1560G= (n.428-1560G=)
c.834G= (p.Arg278=)
c.831G= (p.Arg277=)
c.635-1560G= (n.635-1560G=)
1g.161544759C>GCA1211382FCGR3Ac.516G>C (p.Arg172Ser)
c.519G>C (p.Arg173Ser)
c.627G>C (p.Arg209Ser)
n.569G>C
c.624G>C (p.Arg208Ser)
c.428-1560G>C (n.428-1560G>C)
c.834G>C (p.Arg278Ser)
c.831G>C (p.Arg277Ser)
c.635-1560G>C (n.635-1560G>C)
dbSNP ExAC gnomAD
1g.161544759C>TCA1211381FCGR3Ac.516G>A (p.Arg172=)
c.519G>A (p.Arg173=)
c.627G>A (p.Arg209=)
n.569G>A
c.624G>A (p.Arg208=)
c.428-1560G>A (n.428-1560G>A)
c.834G>A (p.Arg278=)
c.831G>A (p.Arg277=)
c.635-1560G>A (n.635-1560G>A)
dbSNP ExAC gnomAD
1g.161544760C>ACA343367458FCGR3Ac.515G>T (p.Arg172Met)
c.518G>T (p.Arg173Met)
c.626G>T (p.Arg209Met)
n.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.515G>C (p.Arg172Thr)
c.518G>C (p.Arg173Thr)
c.626G>C (p.Arg209Thr)
n.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.515G>A (p.Arg172Lys)
c.518G>A (p.Arg173Lys)
c.626G>A (p.Arg209Lys)
n.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)
1g.161544760_161544761delinsCTCA1202785226FCGR3Ac.514_515delinsAG (p.Arg172=)
c.517_518delinsAG (p.Arg173=)
c.625_626delinsAG (p.Arg209=)
n.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.514del (p.Arg172GlyfsTer14)
c.517del (p.Arg173GlyfsTer14)
c.625del (p.Arg209GlyfsTer14)
n.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
1g.161544761T>ACA343367462FCGR3Ac.514A>T (p.Arg172Trp)
c.517A>T (p.Arg173Trp)
c.625A>T (p.Arg209Trp)
n.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)
1g.161544761T>CCA343367464FCGR3Ac.514A>G (p.Arg172Gly)
c.517A>G (p.Arg173Gly)
c.625A>G (p.Arg209Gly)
n.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.514A>C (p.Arg172=)
c.517A>C (p.Arg173=)
c.625A>C (p.Arg209=)
n.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.514A= (p.Arg172=)
c.517A= (p.Arg173=)
c.625A= (p.Arg209=)
n.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.513C>T (p.Cys171=)
c.516C>T (p.Cys172=)
c.624C>T (p.Cys208=)
n.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
1g.161544762G>CCA343367468FCGR3Ac.513C>G (p.Cys171Trp)
c.516C>G (p.Cys172Trp)
c.624C>G (p.Cys208Trp)
n.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.513C= (p.Cys171=)
c.516C= (p.Cys172=)
c.624C= (p.Cys208=)
n.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.513C>A (p.Cys171Ter)
c.516C>A (p.Cys172Ter)
c.624C>A (p.Cys208Ter)
n.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)
1g.161544763C>ACA1211385FCGR3Ac.512G>T (p.Cys171Phe)
c.515G>T (p.Cys172Phe)
c.623G>T (p.Cys208Phe)
n.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)
dbSNP ExAC gnomAD
1g.161544763C=CA1149151868FCGR3Ac.512G= (p.Cys171=)
c.515G= (p.Cys172=)
c.623G= (p.Cys208=)
n.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.512G>C (p.Cys171Ser)
c.515G>C (p.Cys172Ser)
c.623G>C (p.Cys208Ser)
n.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.512G>A (p.Cys171Tyr)
c.515G>A (p.Cys172Tyr)
c.623G>A (p.Cys208Tyr)
n.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)
gnomAD
1g.161544764A=CA1202785229FCGR3Ac.511T= (p.Cys171=)
c.514T= (p.Cys172=)
c.622T= (p.Cys208=)
n.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.511T>G (p.Cys171Gly)
c.514T>G (p.Cys172Gly)
c.622T>G (p.Cys208Gly)
n.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.511T>C (p.Cys171Arg)
c.514T>C (p.Cys172Arg)
c.622T>C (p.Cys208Arg)
n.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)
COSMIC
1g.161544764A>TCA343367478FCGR3Ac.511T>A (p.Cys171Ser)
c.514T>A (p.Cys172Ser)
c.622T>A (p.Cys208Ser)
n.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)

Number of alleles fetched