| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 1 | g.161544750A>C | CA343367427 | FCGR3A | c.528T>G (p.Phe176Leu) c.525T>G (p.Phe175Leu) c.477T>G (p.Phe159Leu) c.636T>G (p.Phe212Leu) c.578T>G c.633T>G (p.Phe211Leu) c.428-1551T>G (n.428-1551T>G) c.843T>G (p.Phe281Leu) c.840T>G (p.Phe280Leu) c.635-1551T>G (n.635-1551T>G) | |
| 1 | g.161544750A>G | CA421612435 | FCGR3A | c.528T>C (p.Phe176=) c.525T>C (p.Phe175=) c.477T>C (p.Phe159=) c.636T>C (p.Phe212=) c.578T>C c.633T>C (p.Phe211=) c.428-1551T>C (n.428-1551T>C) c.843T>C (p.Phe281=) c.840T>C (p.Phe280=) c.635-1551T>C (n.635-1551T>C) | |
| 1 | g.161544750A>T | CA343367429 | FCGR3A | c.528T>A (p.Phe176Leu) c.525T>A (p.Phe175Leu) c.477T>A (p.Phe159Leu) c.636T>A (p.Phe212Leu) c.578T>A c.633T>A (p.Phe211Leu) c.428-1551T>A (n.428-1551T>A) c.843T>A (p.Phe281Leu) c.840T>A (p.Phe280Leu) c.635-1551T>A (n.635-1551T>A) | |
| 1 | g.161544754del | CA2648790074 | FCGR3A | c.528del (p.Phe176LeufsTer11) c.525del (p.Phe175LeufsTer11) c.477del (p.Phe159LeufsTer11) c.636del (p.Phe212LeufsTer11) c.578del c.633del (p.Phe211LeufsTer11) c.428-1551del (n.428-1551del) c.843del (p.Phe281LeufsTer11) c.840del (p.Phe280LeufsTer11) c.635-1551del (n.635-1551del) | gnomAD v4 |
| 1 | g.161544751A>C | CA343367430 | FCGR3A | c.527T>G (p.Phe176Cys) c.524T>G (p.Phe175Cys) c.476T>G (p.Phe159Cys) c.635T>G (p.Phe212Cys) c.577T>G c.632T>G (p.Phe211Cys) c.428-1552T>G (n.428-1552T>G) c.842T>G (p.Phe281Cys) c.839T>G (p.Phe280Cys) c.635-1552T>G (n.635-1552T>G) | |
| 1 | g.161544751A>G | CA343367431 | FCGR3A | c.527T>C (p.Phe176Ser) c.524T>C (p.Phe175Ser) c.476T>C (p.Phe159Ser) c.635T>C (p.Phe212Ser) c.577T>C c.632T>C (p.Phe211Ser) c.428-1552T>C (n.428-1552T>C) c.842T>C (p.Phe281Ser) c.839T>C (p.Phe280Ser) c.635-1552T>C (n.635-1552T>C) | gnomAD v4 |
| 1 | g.161544751A>T | CA343367433 | FCGR3A | c.527T>A (p.Phe176Tyr) c.524T>A (p.Phe175Tyr) c.476T>A (p.Phe159Tyr) c.635T>A (p.Phe212Tyr) c.577T>A c.632T>A (p.Phe211Tyr) c.428-1552T>A (n.428-1552T>A) c.842T>A (p.Phe281Tyr) c.839T>A (p.Phe280Tyr) c.635-1552T>A (n.635-1552T>A) | |
| 1 | g.161544752A= | CA1139793706 | FCGR3A | c.526T= (p.Phe176=) c.523T= (p.Phe175=) c.475T= (p.Phe159=) c.634T= (p.Phe212=) c.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=) | |
| 1 | g.161544752A>C | CA1211378 | FCGR3A | c.526T>G (p.Phe176Val) c.523T>G (p.Phe175Val) c.475T>G (p.Phe159Val) c.634T>G (p.Phe212Val) c.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 v2 gnomAD v3 gnomAD v4 |
| 1 | g.161544752A>G | CA1211379 | FCGR3A | c.526T>C (p.Phe176Leu) c.523T>C (p.Phe175Leu) c.475T>C (p.Phe159Leu) c.634T>C (p.Phe212Leu) c.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 v2 gnomAD v4 |
| 1 | g.161544752A>T | CA343367436 | FCGR3A | c.526T>A (p.Phe176Ile) c.523T>A (p.Phe175Ile) c.475T>A (p.Phe159Ile) c.634T>A (p.Phe212Ile) c.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) | dbSNP gnomAD v4 |
| 1 | g.161544753A>C | CA421612439 | FCGR3A | c.525T>G (p.Leu175=) c.522T>G (p.Leu174=) c.474T>G (p.Leu158=) c.633T>G (p.Leu211=) c.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) | |
| 1 | g.161544753A>G | CA421612440 | FCGR3A | c.525T>C (p.Leu175=) c.522T>C (p.Leu174=) c.474T>C (p.Leu158=) c.633T>C (p.Leu211=) c.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) | |
| 1 | g.161544753A>T | CA421612441 | FCGR3A | c.525T>A (p.Leu175=) c.522T>A (p.Leu174=) c.474T>A (p.Leu158=) c.633T>A (p.Leu211=) c.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) | |
| 1 | g.161544754A>C | CA343367438 | FCGR3A | c.524T>G (p.Leu175Arg) c.521T>G (p.Leu174Arg) c.473T>G (p.Leu158Arg) c.632T>G (p.Leu211Arg) c.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) | gnomAD v4 |
| 1 | g.161544754A>G | CA343367440 | FCGR3A | c.524T>C (p.Leu175Pro) c.521T>C (p.Leu174Pro) c.473T>C (p.Leu158Pro) c.632T>C (p.Leu211Pro) c.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) | |
| 1 | g.161544754A>T | CA343367442 | FCGR3A | c.524T>A (p.Leu175His) c.521T>A (p.Leu174His) c.473T>A (p.Leu158His) c.632T>A (p.Leu211His) c.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) | |
| 1 | g.161544755G>A | CA343367443 | FCGR3A | c.523C>T (p.Leu175Phe) c.520C>T (p.Leu174Phe) c.472C>T (p.Leu158Phe) c.631C>T (p.Leu211Phe) c.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) | gnomAD v4 |
| 1 | g.161544755G>C | CA343367444 | FCGR3A | c.523C>G (p.Leu175Val) c.520C>G (p.Leu174Val) c.472C>G (p.Leu158Val) c.631C>G (p.Leu211Val) c.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) | |
| 1 | g.161544755G= | CA1202785223 | FCGR3A | c.523C= (p.Leu175=) c.520C= (p.Leu174=) c.472C= (p.Leu158=) c.631C= (p.Leu211=) c.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=) | |
| 1 | g.161544755G>T | CA343367445 | FCGR3A | c.523C>A (p.Leu175Ile) c.520C>A (p.Leu174Ile) c.472C>A (p.Leu158Ile) c.631C>A (p.Leu211Ile) c.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) | |
| 1 | g.161544756C>A | CA421612442 | FCGR3A | c.522G>T (p.Gly174=) c.519G>T (p.Gly173=) c.471G>T (p.Gly157=) c.630G>T (p.Gly210=) c.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) | gnomAD v4 |
| 1 | g.161544756C>G | CA421612443 | FCGR3A | c.522G>C (p.Gly174=) c.519G>C (p.Gly173=) c.471G>C (p.Gly157=) c.630G>C (p.Gly210=) c.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) | |
| 1 | g.161544756C>T | CA421612445 | FCGR3A | c.522G>A (p.Gly174=) c.519G>A (p.Gly173=) c.471G>A (p.Gly157=) c.630G>A (p.Gly210=) c.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) | gnomAD v4 COSMIC |
| 1 | g.161544760dup | CA527135442 | FCGR3A | c.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 |
| 1 | g.161544760del | CA2648790075 | FCGR3A | c.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 |
| 1 | g.161544757C>A | CA343367450 | FCGR3A | c.521G>T (p.Gly174Val) c.518G>T (p.Gly173Val) c.470G>T (p.Gly157Val) c.629G>T (p.Gly210Val) c.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) | |
| 1 | g.161544757C= | CA1202785224 | FCGR3A | c.521G= (p.Gly174=) c.518G= (p.Gly173=) c.470G= (p.Gly157=) c.629G= (p.Gly210=) c.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=) | |
| 1 | g.161544757C>G | CA343367448 | FCGR3A | c.521G>C (p.Gly174Ala) c.518G>C (p.Gly173Ala) c.470G>C (p.Gly157Ala) c.629G>C (p.Gly210Ala) c.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) | |
| 1 | g.161544757C>T | CA1211380 | FCGR3A | c.521G>A (p.Gly174Glu) c.518G>A (p.Gly173Glu) c.470G>A (p.Gly157Glu) c.629G>A (p.Gly210Glu) c.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 v2 gnomAD v4 |
| 1 | g.161544757_161544758insA | CA2648790076 | FCGR3A | c.520_521insT (p.Gly174ValfsTer6) c.517_518insT (p.Gly173ValfsTer6) c.469_470insT (p.Gly157ValfsTer6) c.628_629insT (p.Gly210ValfsTer6) c.570_571insT c.625_626insT (p.Gly209ValfsTer6) c.428-1559_428-1558insT (n.428-1559_428-1558insT) c.835_836insT (p.Gly279ValfsTer6) c.832_833insT (p.Gly278ValfsTer6) c.635-1559_635-1558insT (n.635-1559_635-1558insT) | gnomAD v4 |
| 1 | g.161544758C>A | CA343367452 | FCGR3A | c.520G>T (p.Gly174Trp) c.517G>T (p.Gly173Trp) c.469G>T (p.Gly157Trp) c.628G>T (p.Gly210Trp) c.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) | |
| 1 | g.161544758C>G | CA343367455 | FCGR3A | c.520G>C (p.Gly174Arg) c.517G>C (p.Gly173Arg) c.469G>C (p.Gly157Arg) c.628G>C (p.Gly210Arg) c.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) | |
| 1 | g.161544758C>T | CA343367453 | FCGR3A | c.520G>A (p.Gly174Arg) c.517G>A (p.Gly173Arg) c.469G>A (p.Gly157Arg) c.628G>A (p.Gly210Arg) c.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) | gnomAD v4 |
| 1 | g.161544759C>A | CA343367456 | FCGR3A | c.519G>T (p.Arg173Ser) c.516G>T (p.Arg172Ser) c.468G>T (p.Arg156Ser) c.627G>T (p.Arg209Ser) c.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) | gnomAD v4 |
| 1 | g.161544759C= | CA1202785225 | FCGR3A | c.519G= (p.Arg173=) c.516G= (p.Arg172=) c.468G= (p.Arg156=) c.627G= (p.Arg209=) c.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=) | |
| 1 | g.161544759C>G | CA1211382 | FCGR3A | c.519G>C (p.Arg173Ser) c.516G>C (p.Arg172Ser) c.468G>C (p.Arg156Ser) c.627G>C (p.Arg209Ser) c.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 v2 gnomAD v4 |
| 1 | g.161544759C>T | CA1211381 | FCGR3A | c.519G>A (p.Arg173=) c.516G>A (p.Arg172=) c.468G>A (p.Arg156=) c.627G>A (p.Arg209=) c.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 v2 |
| 1 | g.161544760C>A | CA343367458 | FCGR3A | c.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) | |
| 1 | g.161544760C>G | CA343367459 | FCGR3A | c.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) | |
| 1 | g.161544760C>T | CA343367460 | FCGR3A | c.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 |
| 1 | g.161544760_161544761delinsCT | CA1202785226 | FCGR3A | c.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) | |
| 1 | g.161544761del | CA1211383 | FCGR3A | c.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 |
| 1 | g.161544761T>A | CA343367462 | FCGR3A | c.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 |
| 1 | g.161544761T>C | CA343367464 | FCGR3A | c.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) | |
| 1 | g.161544761T>G | CA421612448 | FCGR3A | c.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) | |
| 1 | g.161544761T= | CA1202785227 | FCGR3A | c.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=) | |
| 1 | g.161544762G>A | CA1211384 | FCGR3A | c.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 |
| 1 | g.161544762G>C | CA343367468 | FCGR3A | c.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) | |
| 1 | g.161544762G= | CA1202785228 | FCGR3A | c.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=) |