| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 1 | g.161544701C>A | CA343367312 | FCGR3A | c.577G>T (p.Gly193Cys) c.574G>T (p.Gly192Cys) c.526G>T (p.Gly176Cys) c.685G>T (p.Gly229Cys) c.627G>T c.682G>T (p.Gly228Cys) c.428-1502G>T (n.428-1502G>T) c.892G>T (p.Gly298Cys) c.889G>T (p.Gly297Cys) c.635-1502G>T (n.635-1502G>T) | |
| 1 | g.161544701C>G | CA343367313 | FCGR3A | c.577G>C (p.Gly193Arg) c.574G>C (p.Gly192Arg) c.526G>C (p.Gly176Arg) c.685G>C (p.Gly229Arg) c.627G>C c.682G>C (p.Gly228Arg) c.428-1502G>C (n.428-1502G>C) c.892G>C (p.Gly298Arg) c.889G>C (p.Gly297Arg) c.635-1502G>C (n.635-1502G>C) | |
| 1 | g.161544701C>T | CA343367314 | FCGR3A | c.577G>A (p.Gly193Ser) c.574G>A (p.Gly192Ser) c.526G>A (p.Gly176Ser) c.685G>A (p.Gly229Ser) c.627G>A c.682G>A (p.Gly228Ser) c.428-1502G>A (n.428-1502G>A) c.892G>A (p.Gly298Ser) c.889G>A (p.Gly297Ser) c.635-1502G>A (n.635-1502G>A) | COSMIC |
| 1 | g.161544702T>A | CA343367315 | FCGR3A | c.576A>T (p.Gln192His) c.573A>T (p.Gln191His) c.525A>T (p.Gln175His) c.684A>T (p.Gln228His) c.626A>T c.681A>T (p.Gln227His) c.428-1503A>T (n.428-1503A>T) c.891A>T (p.Gln297His) c.888A>T (p.Gln296His) c.635-1503A>T (n.635-1503A>T) | |
| 1 | g.161544702T>C | CA1211371 | FCGR3A | c.576A>G (p.Gln192=) c.573A>G (p.Gln191=) c.525A>G (p.Gln175=) c.684A>G (p.Gln228=) c.626A>G c.681A>G (p.Gln227=) c.428-1503A>G (n.428-1503A>G) c.891A>G (p.Gln297=) c.888A>G (p.Gln296=) c.635-1503A>G (n.635-1503A>G) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 1 | g.161544702T>G | CA343367316 | FCGR3A | c.576A>C (p.Gln192His) c.573A>C (p.Gln191His) c.525A>C (p.Gln175His) c.684A>C (p.Gln228His) c.626A>C c.681A>C (p.Gln227His) c.428-1503A>C (n.428-1503A>C) c.891A>C (p.Gln297His) c.888A>C (p.Gln296His) c.635-1503A>C (n.635-1503A>C) | |
| 1 | g.161544702T= | CA1143939801 | FCGR3A | c.576A= (p.Gln192=) c.573A= (p.Gln191=) c.525A= (p.Gln175=) c.684A= (p.Gln228=) c.626A= c.681A= (p.Gln227=) c.428-1503A= (n.428-1503A=) c.891A= (p.Gln297=) c.888A= (p.Gln296=) c.635-1503A= (n.635-1503A=) | |
| 1 | g.161544703T>A | CA343367317 | FCGR3A | c.575A>T (p.Gln192Leu) c.572A>T (p.Gln191Leu) c.524A>T (p.Gln175Leu) c.683A>T (p.Gln228Leu) c.625A>T c.680A>T (p.Gln227Leu) c.428-1504A>T (n.428-1504A>T) c.890A>T (p.Gln297Leu) c.887A>T (p.Gln296Leu) c.635-1504A>T (n.635-1504A>T) | |
| 1 | g.161544703T>C | CA343367319 | FCGR3A | c.575A>G (p.Gln192Arg) c.572A>G (p.Gln191Arg) c.524A>G (p.Gln175Arg) c.683A>G (p.Gln228Arg) c.625A>G c.680A>G (p.Gln227Arg) c.428-1504A>G (n.428-1504A>G) c.890A>G (p.Gln297Arg) c.887A>G (p.Gln296Arg) c.635-1504A>G (n.635-1504A>G) | dbSNP gnomAD v2 gnomAD v4 |
| 1 | g.161544703T>G | CA343367318 | FCGR3A | c.575A>C (p.Gln192Pro) c.572A>C (p.Gln191Pro) c.524A>C (p.Gln175Pro) c.683A>C (p.Gln228Pro) c.625A>C c.680A>C (p.Gln227Pro) c.428-1504A>C (n.428-1504A>C) c.890A>C (p.Gln297Pro) c.887A>C (p.Gln296Pro) c.635-1504A>C (n.635-1504A>C) | |
| 1 | g.161544703T= | CA1202785206 | FCGR3A | c.575A= (p.Gln192=) c.572A= (p.Gln191=) c.524A= (p.Gln175=) c.683A= (p.Gln228=) c.625A= c.680A= (p.Gln227=) c.428-1504A= (n.428-1504A=) c.890A= (p.Gln297=) c.887A= (p.Gln296=) c.635-1504A= (n.635-1504A=) | |
| 1 | g.161544704G>A | CA343367320 | FCGR3A | c.574C>T (p.Gln192Ter) c.571C>T (p.Gln191Ter) c.523C>T (p.Gln175Ter) c.682C>T (p.Gln228Ter) c.624C>T c.679C>T (p.Gln227Ter) c.428-1505C>T (n.428-1505C>T) c.889C>T (p.Gln297Ter) c.886C>T (p.Gln296Ter) c.635-1505C>T (n.635-1505C>T) | |
| 1 | g.161544704G>C | CA343367322 | FCGR3A | c.574C>G (p.Gln192Glu) c.571C>G (p.Gln191Glu) c.523C>G (p.Gln175Glu) c.682C>G (p.Gln228Glu) c.624C>G c.679C>G (p.Gln227Glu) c.428-1505C>G (n.428-1505C>G) c.889C>G (p.Gln297Glu) c.886C>G (p.Gln296Glu) c.635-1505C>G (n.635-1505C>G) | |
| 1 | g.161544704G>T | CA343367321 | FCGR3A | c.574C>A (p.Gln192Lys) c.571C>A (p.Gln191Lys) c.523C>A (p.Gln175Lys) c.682C>A (p.Gln228Lys) c.624C>A c.679C>A (p.Gln227Lys) c.428-1505C>A (n.428-1505C>A) c.889C>A (p.Gln297Lys) c.886C>A (p.Gln296Lys) c.635-1505C>A (n.635-1505C>A) | gnomAD v4 |
| 1 | g.161544705A>C | CA421612318 | FCGR3A | c.573T>G (p.Thr191=) c.570T>G (p.Thr190=) c.522T>G (p.Thr174=) c.681T>G (p.Thr227=) c.623T>G c.678T>G (p.Thr226=) c.428-1506T>G (n.428-1506T>G) c.888T>G (p.Thr296=) c.885T>G (p.Thr295=) c.635-1506T>G (n.635-1506T>G) | |
| 1 | g.161544705A>G | CA421612320 | FCGR3A | c.573T>C (p.Thr191=) c.570T>C (p.Thr190=) c.522T>C (p.Thr174=) c.681T>C (p.Thr227=) c.623T>C c.678T>C (p.Thr226=) c.428-1506T>C (n.428-1506T>C) c.888T>C (p.Thr296=) c.885T>C (p.Thr295=) c.635-1506T>C (n.635-1506T>C) | |
| 1 | g.161544705A>T | CA421612321 | FCGR3A | c.573T>A (p.Thr191=) c.570T>A (p.Thr190=) c.522T>A (p.Thr174=) c.681T>A (p.Thr227=) c.623T>A c.678T>A (p.Thr226=) c.428-1506T>A (n.428-1506T>A) c.888T>A (p.Thr296=) c.885T>A (p.Thr295=) c.635-1506T>A (n.635-1506T>A) | |
| 1 | g.161544706G>A | CA1211372 | FCGR3A | c.572C>T (p.Thr191Ile) c.569C>T (p.Thr190Ile) c.521C>T (p.Thr174Ile) c.680C>T (p.Thr227Ile) c.622C>T c.677C>T (p.Thr226Ile) c.428-1507C>T (n.428-1507C>T) c.887C>T (p.Thr296Ile) c.884C>T (p.Thr295Ile) c.635-1507C>T (n.635-1507C>T) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 1 | g.161544706G>C | CA343367323 | FCGR3A | c.572C>G (p.Thr191Ser) c.569C>G (p.Thr190Ser) c.521C>G (p.Thr174Ser) c.680C>G (p.Thr227Ser) c.622C>G c.677C>G (p.Thr226Ser) c.428-1507C>G (n.428-1507C>G) c.887C>G (p.Thr296Ser) c.884C>G (p.Thr295Ser) c.635-1507C>G (n.635-1507C>G) | |
| 1 | g.161544706G= | CA1202785207 | FCGR3A | c.572C= (p.Thr191=) c.569C= (p.Thr190=) c.521C= (p.Thr174=) c.680C= (p.Thr227=) c.622C= c.677C= (p.Thr226=) c.428-1507C= (n.428-1507C=) c.887C= (p.Thr296=) c.884C= (p.Thr295=) c.635-1507C= (n.635-1507C=) | |
| 1 | g.161544706G>T | CA1211373 | FCGR3A | c.572C>A (p.Thr191Asn) c.569C>A (p.Thr190Asn) c.521C>A (p.Thr174Asn) c.680C>A (p.Thr227Asn) c.622C>A c.677C>A (p.Thr226Asn) c.428-1507C>A (n.428-1507C>A) c.887C>A (p.Thr296Asn) c.884C>A (p.Thr295Asn) c.635-1507C>A (n.635-1507C>A) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 1 | g.161544707T>A | CA343367324 | FCGR3A | c.571A>T (p.Thr191Ser) c.568A>T (p.Thr190Ser) c.520A>T (p.Thr174Ser) c.679A>T (p.Thr227Ser) c.621A>T c.676A>T (p.Thr226Ser) c.428-1508A>T (n.428-1508A>T) c.886A>T (p.Thr296Ser) c.883A>T (p.Thr295Ser) c.635-1508A>T (n.635-1508A>T) | |
| 1 | g.161544707T>C | CA343367325 | FCGR3A | c.571A>G (p.Thr191Ala) c.568A>G (p.Thr190Ala) c.520A>G (p.Thr174Ala) c.679A>G (p.Thr227Ala) c.621A>G c.676A>G (p.Thr226Ala) c.428-1508A>G (n.428-1508A>G) c.886A>G (p.Thr296Ala) c.883A>G (p.Thr295Ala) c.635-1508A>G (n.635-1508A>G) | |
| 1 | g.161544707T>G | CA343367326 | FCGR3A | c.571A>C (p.Thr191Pro) c.568A>C (p.Thr190Pro) c.520A>C (p.Thr174Pro) c.679A>C (p.Thr227Pro) c.621A>C c.676A>C (p.Thr226Pro) c.428-1508A>C (n.428-1508A>C) c.886A>C (p.Thr296Pro) c.883A>C (p.Thr295Pro) c.635-1508A>C (n.635-1508A>C) | dbSNP |
| 1 | g.161544707T= | CA1202785208 | FCGR3A | c.571A= (p.Thr191=) c.568A= (p.Thr190=) c.520A= (p.Thr174=) c.679A= (p.Thr227=) c.621A= c.676A= (p.Thr226=) c.428-1508A= (n.428-1508A=) c.886A= (p.Thr296=) c.883A= (p.Thr295=) c.635-1508A= (n.635-1508A=) | |
| 1 | g.161544708G>A | CA421612329 | FCGR3A | c.570C>T (p.Ile190=) c.567C>T (p.Ile189=) c.519C>T (p.Ile173=) c.678C>T (p.Ile226=) c.620C>T c.675C>T (p.Ile225=) c.428-1509C>T (n.428-1509C>T) c.885C>T (p.Ile295=) c.882C>T (p.Ile294=) c.635-1509C>T (n.635-1509C>T) | dbSNP gnomAD v3 gnomAD v4 |
| 1 | g.161544708G>C | CA343367327 | FCGR3A | c.570C>G (p.Ile190Met) c.567C>G (p.Ile189Met) c.519C>G (p.Ile173Met) c.678C>G (p.Ile226Met) c.620C>G c.675C>G (p.Ile225Met) c.428-1509C>G (n.428-1509C>G) c.885C>G (p.Ile295Met) c.882C>G (p.Ile294Met) c.635-1509C>G (n.635-1509C>G) | |
| 1 | g.161544708G= | CA1202785209 | FCGR3A | c.570C= (p.Ile190=) c.567C= (p.Ile189=) c.519C= (p.Ile173=) c.678C= (p.Ile226=) c.620C= c.675C= (p.Ile225=) c.428-1509C= (n.428-1509C=) c.885C= (p.Ile295=) c.882C= (p.Ile294=) c.635-1509C= (n.635-1509C=) | |
| 1 | g.161544708G>T | CA421612332 | FCGR3A | c.570C>A (p.Ile190=) c.567C>A (p.Ile189=) c.519C>A (p.Ile173=) c.678C>A (p.Ile226=) c.620C>A c.675C>A (p.Ile225=) c.428-1509C>A (n.428-1509C>A) c.885C>A (p.Ile295=) c.882C>A (p.Ile294=) c.635-1509C>A (n.635-1509C>A) | dbSNP |
| 1 | g.161544709A>C | CA343367328 | FCGR3A | c.569T>G (p.Ile190Ser) c.566T>G (p.Ile189Ser) c.518T>G (p.Ile173Ser) c.677T>G (p.Ile226Ser) c.619T>G c.674T>G (p.Ile225Ser) c.428-1510T>G (n.428-1510T>G) c.884T>G (p.Ile295Ser) c.881T>G (p.Ile294Ser) c.635-1510T>G (n.635-1510T>G) | |
| 1 | g.161544709A>G | CA343367329 | FCGR3A | c.569T>C (p.Ile190Thr) c.566T>C (p.Ile189Thr) c.518T>C (p.Ile173Thr) c.677T>C (p.Ile226Thr) c.619T>C c.674T>C (p.Ile225Thr) c.428-1510T>C (n.428-1510T>C) c.884T>C (p.Ile295Thr) c.881T>C (p.Ile294Thr) c.635-1510T>C (n.635-1510T>C) | gnomAD v4 |
| 1 | g.161544709A>T | CA343367330 | FCGR3A | c.569T>A (p.Ile190Asn) c.566T>A (p.Ile189Asn) c.518T>A (p.Ile173Asn) c.677T>A (p.Ile226Asn) c.619T>A c.674T>A (p.Ile225Asn) c.428-1510T>A (n.428-1510T>A) c.884T>A (p.Ile295Asn) c.881T>A (p.Ile294Asn) c.635-1510T>A (n.635-1510T>A) | |
| 1 | g.161544710T>A | CA343367331 | FCGR3A | c.568A>T (p.Ile190Phe) c.565A>T (p.Ile189Phe) c.517A>T (p.Ile173Phe) c.676A>T (p.Ile226Phe) c.618A>T c.673A>T (p.Ile225Phe) c.428-1511A>T (n.428-1511A>T) c.883A>T (p.Ile295Phe) c.880A>T (p.Ile294Phe) c.635-1511A>T (n.635-1511A>T) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 1 | g.161544710T>C | CA343367332 | FCGR3A | c.568A>G (p.Ile190Val) c.565A>G (p.Ile189Val) c.517A>G (p.Ile173Val) c.676A>G (p.Ile226Val) c.618A>G c.673A>G (p.Ile225Val) c.428-1511A>G (n.428-1511A>G) c.883A>G (p.Ile295Val) c.880A>G (p.Ile294Val) c.635-1511A>G (n.635-1511A>G) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 1 | g.161544710T>G | CA343367333 | FCGR3A | c.568A>C (p.Ile190Leu) c.565A>C (p.Ile189Leu) c.517A>C (p.Ile173Leu) c.676A>C (p.Ile226Leu) c.618A>C c.673A>C (p.Ile225Leu) c.428-1511A>C (n.428-1511A>C) c.883A>C (p.Ile295Leu) c.880A>C (p.Ile294Leu) c.635-1511A>C (n.635-1511A>C) | |
| 1 | g.161544710T= | CA1202785210 | FCGR3A | c.568A= (p.Ile190=) c.565A= (p.Ile189=) c.517A= (p.Ile173=) c.676A= (p.Ile226=) c.618A= c.673A= (p.Ile225=) c.428-1511A= (n.428-1511A=) c.883A= (p.Ile295=) c.880A= (p.Ile294=) c.635-1511A= (n.635-1511A=) | |
| 1 | g.161544711G>A | CA1211374 | FCGR3A | c.567C>T (p.Thr189=) c.564C>T (p.Thr188=) c.516C>T (p.Thr172=) c.675C>T (p.Thr225=) c.617C>T c.672C>T (p.Thr224=) c.428-1512C>T (n.428-1512C>T) c.882C>T (p.Thr294=) c.879C>T (p.Thr293=) c.635-1512C>T (n.635-1512C>T) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 1 | g.161544711G>C | CA421612336 | FCGR3A | c.567C>G (p.Thr189=) c.564C>G (p.Thr188=) c.516C>G (p.Thr172=) c.675C>G (p.Thr225=) c.617C>G c.672C>G (p.Thr224=) c.428-1512C>G (n.428-1512C>G) c.882C>G (p.Thr294=) c.879C>G (p.Thr293=) c.635-1512C>G (n.635-1512C>G) | |
| 1 | g.161544711G= | CA1202785211 | FCGR3A | c.567C= (p.Thr189=) c.564C= (p.Thr188=) c.516C= (p.Thr172=) c.675C= (p.Thr225=) c.617C= c.672C= (p.Thr224=) c.428-1512C= (n.428-1512C=) c.882C= (p.Thr294=) c.879C= (p.Thr293=) c.635-1512C= (n.635-1512C=) | |
| 1 | g.161544711G>T | CA421612338 | FCGR3A | c.567C>A (p.Thr189=) c.564C>A (p.Thr188=) c.516C>A (p.Thr172=) c.675C>A (p.Thr225=) c.617C>A c.672C>A (p.Thr224=) c.428-1512C>A (n.428-1512C>A) c.882C>A (p.Thr294=) c.879C>A (p.Thr293=) c.635-1512C>A (n.635-1512C>A) | |
| 1 | g.161544712G>A | CA343367336 | FCGR3A | c.566C>T (p.Thr189Ile) c.563C>T (p.Thr188Ile) c.515C>T (p.Thr172Ile) c.674C>T (p.Thr225Ile) c.616C>T c.671C>T (p.Thr224Ile) c.428-1513C>T (n.428-1513C>T) c.881C>T (p.Thr294Ile) c.878C>T (p.Thr293Ile) c.635-1513C>T (n.635-1513C>T) | gnomAD v4 |
| 1 | g.161544712G>C | CA343367334 | FCGR3A | c.566C>G (p.Thr189Ser) c.563C>G (p.Thr188Ser) c.515C>G (p.Thr172Ser) c.674C>G (p.Thr225Ser) c.616C>G c.671C>G (p.Thr224Ser) c.428-1513C>G (n.428-1513C>G) c.881C>G (p.Thr294Ser) c.878C>G (p.Thr293Ser) c.635-1513C>G (n.635-1513C>G) | |
| 1 | g.161544712G>T | CA343367335 | FCGR3A | c.566C>A (p.Thr189Asn) c.563C>A (p.Thr188Asn) c.515C>A (p.Thr172Asn) c.674C>A (p.Thr225Asn) c.616C>A c.671C>A (p.Thr224Asn) c.428-1513C>A (n.428-1513C>A) c.881C>A (p.Thr294Asn) c.878C>A (p.Thr293Asn) c.635-1513C>A (n.635-1513C>A) | |
| 1 | g.161544713T>A | CA343367337 | FCGR3A | c.565A>T (p.Thr189Ser) c.562A>T (p.Thr188Ser) c.514A>T (p.Thr172Ser) c.673A>T (p.Thr225Ser) c.615A>T c.670A>T (p.Thr224Ser) c.428-1514A>T (n.428-1514A>T) c.880A>T (p.Thr294Ser) c.877A>T (p.Thr293Ser) c.635-1514A>T (n.635-1514A>T) | |
| 1 | g.161544713T>C | CA343367338 | FCGR3A | c.565A>G (p.Thr189Ala) c.562A>G (p.Thr188Ala) c.514A>G (p.Thr172Ala) c.673A>G (p.Thr225Ala) c.615A>G c.670A>G (p.Thr224Ala) c.428-1514A>G (n.428-1514A>G) c.880A>G (p.Thr294Ala) c.877A>G (p.Thr293Ala) c.635-1514A>G (n.635-1514A>G) | |
| 1 | g.161544713T>G | CA343367339 | FCGR3A | c.565A>C (p.Thr189Pro) c.562A>C (p.Thr188Pro) c.514A>C (p.Thr172Pro) c.673A>C (p.Thr225Pro) c.615A>C c.670A>C (p.Thr224Pro) c.428-1514A>C (n.428-1514A>C) c.880A>C (p.Thr294Pro) c.877A>C (p.Thr293Pro) c.635-1514A>C (n.635-1514A>C) | |
| 1 | g.161544714G>A | CA421612342 | FCGR3A | c.564C>T (p.Ile188=) c.561C>T (p.Ile187=) c.513C>T (p.Ile171=) c.672C>T (p.Ile224=) c.614C>T c.669C>T (p.Ile223=) c.428-1515C>T (n.428-1515C>T) c.879C>T (p.Ile293=) c.876C>T (p.Ile292=) c.635-1515C>T (n.635-1515C>T) | COSMIC |
| 1 | g.161544714G>C | CA343367340 | FCGR3A | c.564C>G (p.Ile188Met) c.561C>G (p.Ile187Met) c.513C>G (p.Ile171Met) c.672C>G (p.Ile224Met) c.614C>G c.669C>G (p.Ile223Met) c.428-1515C>G (n.428-1515C>G) c.879C>G (p.Ile293Met) c.876C>G (p.Ile292Met) c.635-1515C>G (n.635-1515C>G) | |
| 1 | g.161544714G>T | CA421612340 | FCGR3A | c.564C>A (p.Ile188=) c.561C>A (p.Ile187=) c.513C>A (p.Ile171=) c.672C>A (p.Ile224=) c.614C>A c.669C>A (p.Ile223=) c.428-1515C>A (n.428-1515C>A) c.879C>A (p.Ile293=) c.876C>A (p.Ile292=) c.635-1515C>A (n.635-1515C>A) | |
| 1 | g.161544715A>C | CA343367341 | FCGR3A | c.563T>G (p.Ile188Ser) c.560T>G (p.Ile187Ser) c.512T>G (p.Ile171Ser) c.671T>G (p.Ile224Ser) c.613T>G c.668T>G (p.Ile223Ser) c.428-1516T>G (n.428-1516T>G) c.878T>G (p.Ile293Ser) c.875T>G (p.Ile292Ser) c.635-1516T>G (n.635-1516T>G) |