| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 1 | g.161674017_161674037dup | CA1008429688 | FCGR2B | c.704_724dup (p.Val241_Val242insAlaAlaIleValAlaAlaVal) c.683_703dup (p.Val234_Val235insAlaAlaIleValAlaAlaVal) n.754_774dup n.2072_2092dup c.701_721dup (p.Val240_Val241insAlaAlaIleValAlaAlaVal) c.680_700dup (p.Val233_Val234insAlaAlaIleValAlaAlaVal) n.933_953dup | dbSNP gnomAD v3 gnomAD v4 |
| 1 | g.161674011C>A | CA343367725 | FCGR2B | c.698C>A (p.Ala233Asp) c.677C>A (p.Ala226Asp) n.748C>A n.2066C>A c.695C>A (p.Ala232Asp) c.674C>A (p.Ala225Asp) n.927C>A | gnomAD v4 |
| 1 | g.161674011C>G | CA343367727 | FCGR2B | c.698C>G (p.Ala233Gly) c.677C>G (p.Ala226Gly) n.748C>G n.2066C>G c.695C>G (p.Ala232Gly) c.674C>G (p.Ala225Gly) n.927C>G | |
| 1 | g.161674011C>T | CA343367728 | FCGR2B | c.698C>T (p.Ala233Val) c.677C>T (p.Ala226Val) n.748C>T n.2066C>T c.695C>T (p.Ala232Val) c.674C>T (p.Ala225Val) n.927C>T | |
| 1 | g.161674012T>A | CA421420517 | FCGR2B | c.699T>A (p.Ala233=) c.678T>A (p.Ala226=) n.749T>A n.2067T>A c.696T>A (p.Ala232=) c.675T>A (p.Ala225=) n.928T>A | |
| 1 | g.161674012T>C | CA421420519 | FCGR2B | c.699T>C (p.Ala233=) c.678T>C (p.Ala226=) n.749T>C n.2067T>C c.696T>C (p.Ala232=) c.675T>C (p.Ala225=) n.928T>C | gnomAD v4 |
| 1 | g.161674012T>G | CA421420521 | FCGR2B | c.699T>G (p.Ala233=) c.678T>G (p.Ala226=) n.749T>G n.2067T>G c.696T>G (p.Ala232=) c.675T>G (p.Ala225=) n.928T>G | |
| 1 | g.161674013G>A | CA343367744 | FCGR2B | c.700G>A (p.Val234Ile) c.679G>A (p.Val227Ile) n.750G>A n.2068G>A c.697G>A (p.Val233Ile) c.676G>A (p.Val226Ile) n.929G>A | dbSNP gnomAD v2 gnomAD v4 |
| 1 | g.161674013G>C | CA343367732 | FCGR2B | c.700G>C (p.Val234Leu) c.679G>C (p.Val227Leu) n.750G>C n.2068G>C c.697G>C (p.Val233Leu) c.676G>C (p.Val226Leu) n.929G>C | |
| 1 | g.161674013G= | CA1202839758 | FCGR2B | c.700G= (p.Val234=) c.679G= (p.Val227=) n.750G= n.2068G= c.697G= (p.Val233=) c.676G= (p.Val226=) n.929G= | |
| 1 | g.161674013G>T | CA343367734 | FCGR2B | c.700G>T (p.Val234Leu) c.679G>T (p.Val227Leu) n.750G>T n.2068G>T c.697G>T (p.Val233Leu) c.676G>T (p.Val226Leu) n.929G>T | |
| 1 | g.161674014T>A | CA343367748 | FCGR2B | c.701T>A (p.Val234Glu) c.680T>A (p.Val227Glu) n.751T>A n.2069T>A c.698T>A (p.Val233Glu) c.677T>A (p.Val226Glu) n.930T>A | gnomAD v3 gnomAD v4 |
| 1 | g.161674014T>C | CA343367751 | FCGR2B | c.701T>C (p.Val234Ala) c.680T>C (p.Val227Ala) n.751T>C n.2069T>C c.698T>C (p.Val233Ala) c.677T>C (p.Val226Ala) n.930T>C | |
| 1 | g.161674014T>G | CA343367753 | FCGR2B | c.701T>G (p.Val234Gly) c.680T>G (p.Val227Gly) n.751T>G n.2069T>G c.698T>G (p.Val233Gly) c.677T>G (p.Val226Gly) n.930T>G | gnomAD v4 |
| 1 | g.161674015A= | CA1202839759 | FCGR2B | c.702A= (p.Val234=) c.681A= (p.Val227=) n.752A= n.2070A= c.699A= (p.Val233=) c.678A= (p.Val226=) n.931A= | |
| 1 | g.161674015A>C | CA421420533 | FCGR2B | c.702A>C (p.Val234=) c.681A>C (p.Val227=) n.752A>C n.2070A>C c.699A>C (p.Val233=) c.678A>C (p.Val226=) n.931A>C | |
| 1 | g.161674015A>G | CA421420532 | FCGR2B | c.702A>G (p.Val234=) c.681A>G (p.Val227=) n.752A>G n.2070A>G c.699A>G (p.Val233=) c.678A>G (p.Val226=) n.931A>G | gnomAD v4 |
| 1 | g.161674015A>T | CA421420530 | FCGR2B | c.702A>T (p.Val234=) c.681A>T (p.Val227=) n.752A>T n.2070A>T c.699A>T (p.Val233=) c.678A>T (p.Val226=) n.931A>T | dbSNP gnomAD v3 gnomAD v4 |
| 1 | g.161674016G>A | CA343367758 | FCGR2B | c.703G>A (p.Ala235Thr) c.682G>A (p.Ala228Thr) n.753G>A n.2071G>A c.700G>A (p.Ala234Thr) c.679G>A (p.Ala227Thr) n.932G>A | |
| 1 | g.161674016G>C | CA343367762 | FCGR2B | c.703G>C (p.Ala235Pro) c.682G>C (p.Ala228Pro) n.753G>C n.2071G>C c.700G>C (p.Ala234Pro) c.679G>C (p.Ala227Pro) n.932G>C | gnomAD v4 |
| 1 | g.161674016G= | CA1202839760 | FCGR2B | c.703G= (p.Ala235=) c.682G= (p.Ala228=) n.753G= n.2071G= c.700G= (p.Ala234=) c.679G= (p.Ala227=) n.932G= | |
| 1 | g.161674016G>T | CA343367764 | FCGR2B | c.703G>T (p.Ala235Ser) c.682G>T (p.Ala228Ser) n.753G>T n.2071G>T c.700G>T (p.Ala234Ser) c.679G>T (p.Ala227Ser) n.932G>T | dbSNP gnomAD v2 |
| 1 | g.161674017C>A | CA343367767 | FCGR2B | c.704C>A (p.Ala235Glu) c.683C>A (p.Ala228Glu) n.754C>A n.2072C>A c.701C>A (p.Ala234Glu) c.680C>A (p.Ala227Glu) n.933C>A | gnomAD v4 |
| 1 | g.161674017C= | CA1202839761 | FCGR2B | c.704C= (p.Ala235=) c.683C= (p.Ala228=) n.754C= n.2072C= c.701C= (p.Ala234=) c.680C= (p.Ala227=) n.933C= | |
| 1 | g.161674017C>G | CA343367769 | FCGR2B | c.704C>G (p.Ala235Gly) c.683C>G (p.Ala228Gly) n.754C>G n.2072C>G c.701C>G (p.Ala234Gly) c.680C>G (p.Ala227Gly) n.933C>G | |
| 1 | g.161674017C>T | CA343367772 | FCGR2B | c.704C>T (p.Ala235Val) c.683C>T (p.Ala228Val) n.754C>T n.2072C>T c.701C>T (p.Ala234Val) c.680C>T (p.Ala227Val) n.933C>T | dbSNP gnomAD v2 gnomAD v4 |
| 1 | g.161674018G>A | CA421420542 | FCGR2B | c.705G>A (p.Ala235=) c.684G>A (p.Ala228=) n.755G>A n.2073G>A c.702G>A (p.Ala234=) c.681G>A (p.Ala227=) n.934G>A | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 1 | g.161674018G>C | CA421420544 | FCGR2B | c.705G>C (p.Ala235=) c.684G>C (p.Ala228=) n.755G>C n.2073G>C c.702G>C (p.Ala234=) c.681G>C (p.Ala227=) n.934G>C | |
| 1 | g.161674018G= | CA1202839762 | FCGR2B | c.705G= (p.Ala235=) c.684G= (p.Ala228=) n.755G= n.2073G= c.702G= (p.Ala234=) c.681G= (p.Ala227=) n.934G= | |
| 1 | g.161674018G>T | CA421420545 | FCGR2B | c.705G>T (p.Ala235=) c.684G>T (p.Ala228=) n.755G>T n.2073G>T c.702G>T (p.Ala234=) c.681G>T (p.Ala227=) n.934G>T | gnomAD v4 |
| 1 | g.161674019G>A | CA343367776 | FCGR2B | c.706G>A (p.Ala236Thr) c.685G>A (p.Ala229Thr) n.756G>A n.2074G>A c.703G>A (p.Ala235Thr) c.682G>A (p.Ala228Thr) n.935G>A | dbSNP gnomAD v2 gnomAD v4 |
| 1 | g.161674019G>C | CA343367778 | FCGR2B | c.706G>C (p.Ala236Pro) c.685G>C (p.Ala229Pro) n.756G>C n.2074G>C c.703G>C (p.Ala235Pro) c.682G>C (p.Ala228Pro) n.935G>C | |
| 1 | g.161674019G= | CA1202839763 | FCGR2B | c.706G= (p.Ala236=) c.685G= (p.Ala229=) n.756G= n.2074G= c.703G= (p.Ala235=) c.682G= (p.Ala228=) n.935G= | |
| 1 | g.161674019G>T | CA343367782 | FCGR2B | c.706G>T (p.Ala236Ser) c.685G>T (p.Ala229Ser) n.756G>T n.2074G>T c.703G>T (p.Ala235Ser) c.682G>T (p.Ala228Ser) n.935G>T | gnomAD v4 |
| 1 | g.161674020C>A | CA343367794 | FCGR2B | c.707C>A (p.Ala236Asp) c.686C>A (p.Ala229Asp) n.757C>A n.2075C>A c.704C>A (p.Ala235Asp) c.683C>A (p.Ala228Asp) n.936C>A | |
| 1 | g.161674020C>G | CA343367785 | FCGR2B | c.707C>G (p.Ala236Gly) c.686C>G (p.Ala229Gly) n.757C>G n.2075C>G c.704C>G (p.Ala235Gly) c.683C>G (p.Ala228Gly) n.936C>G | |
| 1 | g.161674020C>T | CA343367792 | FCGR2B | c.707C>T (p.Ala236Val) c.686C>T (p.Ala229Val) n.757C>T n.2075C>T c.704C>T (p.Ala235Val) c.683C>T (p.Ala228Val) n.936C>T | gnomAD v3 gnomAD v4 |
| 1 | g.161674021C>A | CA421420560 | FCGR2B | c.708C>A (p.Ala236=) c.687C>A (p.Ala229=) n.758C>A n.2076C>A c.705C>A (p.Ala235=) c.684C>A (p.Ala228=) n.937C>A | gnomAD v4 |
| 1 | g.161674021C>G | CA421420557 | FCGR2B | c.708C>G (p.Ala236=) c.687C>G (p.Ala229=) n.758C>G n.2076C>G c.705C>G (p.Ala235=) c.684C>G (p.Ala228=) n.937C>G | |
| 1 | g.161674021C>T | CA421420559 | FCGR2B | c.708C>T (p.Ala236=) c.687C>T (p.Ala229=) n.758C>T n.2076C>T c.705C>T (p.Ala235=) c.684C>T (p.Ala228=) n.937C>T | |
| 1 | g.161674022A>C | CA343367798 | FCGR2B | c.709A>C (p.Ile237Leu) c.688A>C (p.Ile230Leu) n.759A>C n.2077A>C c.706A>C (p.Ile236Leu) c.685A>C (p.Ile229Leu) n.938A>C | |
| 1 | g.161674022A>G | CA343367803 | FCGR2B | c.709A>G (p.Ile237Val) c.688A>G (p.Ile230Val) n.759A>G n.2077A>G c.706A>G (p.Ile236Val) c.685A>G (p.Ile229Val) n.938A>G | |
| 1 | g.161674022A>T | CA343367801 | FCGR2B | c.709A>T (p.Ile237Phe) c.688A>T (p.Ile230Phe) n.759A>T n.2077A>T c.706A>T (p.Ile236Phe) c.685A>T (p.Ile229Phe) n.938A>T | |
| 1 | g.161674022_161674025delinsATTG | CA1202839764 | FCGR2B | c.709_712delinsATTG (p.Ile237=) c.688_691delinsATTG (p.Ile230=) n.759_762delinsATTG n.2077_2080delinsATTG c.706_709delinsATTG (p.Ile236=) c.685_688delinsATTG (p.Ile229=) n.938_941delinsATTG | |
| 1 | g.161674023T>A | CA343367809 | FCGR2B | c.710T>A (p.Ile237Asn) c.689T>A (p.Ile230Asn) n.760T>A n.2078T>A c.707T>A (p.Ile236Asn) c.686T>A (p.Ile229Asn) n.939T>A | |
| 1 | g.161674023T>C | CA343367812 | FCGR2B | c.710T>C (p.Ile237Thr) c.689T>C (p.Ile230Thr) n.760T>C n.2078T>C c.707T>C (p.Ile236Thr) c.686T>C (p.Ile229Thr) n.939T>C | |
| 1 | g.161674023T>G | CA343367813 | FCGR2B | c.710T>G (p.Ile237Ser) c.689T>G (p.Ile230Ser) n.760T>G n.2078T>G c.707T>G (p.Ile236Ser) c.686T>G (p.Ile229Ser) n.939T>G | |
| 1 | g.161674026_161674028del | CA1202839765 | FCGR2B | c.713_715del (p.Val238del) c.692_694del (p.Val231del) n.763_765del n.2081_2083del c.710_712del (p.Val237del) c.689_691del (p.Val230del) n.942_944del | dbSNP |
| 1 | g.161674024T>A | CA421420572 | FCGR2B | c.711T>A (p.Ile237=) c.690T>A (p.Ile230=) n.761T>A n.2079T>A c.708T>A (p.Ile236=) c.687T>A (p.Ile229=) n.940T>A | |
| 1 | g.161674024T>C | CA421420574 | FCGR2B | c.711T>C (p.Ile237=) c.690T>C (p.Ile230=) n.761T>C n.2079T>C c.708T>C (p.Ile236=) c.687T>C (p.Ile229=) n.940T>C |