| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 1 | g.161674008T>A | CA343367701 | FCGR2B | c.692T>A (p.Ile231Asn) c.695T>A (p.Ile232Asn) c.674T>A (p.Ile225Asn) c.671T>A (p.Ile224Asn) n.924T>A n.745T>A n.2063T>A | |
| 1 | g.161674008T>C | CA117549 | FCGR2B | c.692T>C (p.Ile231Thr) c.695T>C (p.Ile232Thr) c.674T>C (p.Ile225Thr) c.671T>C (p.Ile224Thr) n.924T>C n.745T>C n.2063T>C | ClinVar dbSNP ExAC gnomAD |
| 1 | g.161674008T>G | CA343367706 | FCGR2B | c.692T>G (p.Ile231Ser) c.695T>G (p.Ile232Ser) c.674T>G (p.Ile225Ser) c.671T>G (p.Ile224Ser) n.924T>G n.745T>G n.2063T>G | |
| 1 | g.161674009T>A | CA421420506 | FCGR2B | c.693T>A (p.Ile231=) c.696T>A (p.Ile232=) c.675T>A (p.Ile225=) c.672T>A (p.Ile224=) n.925T>A n.746T>A n.2064T>A | |
| 1 | g.161674009T>C | CA421420507 | FCGR2B | c.693T>C (p.Ile231=) c.696T>C (p.Ile232=) c.675T>C (p.Ile225=) c.672T>C (p.Ile224=) n.925T>C n.746T>C n.2064T>C | |
| 1 | g.161674009T>G | CA343367709 | FCGR2B | c.693T>G (p.Ile231Met) c.696T>G (p.Ile232Met) c.675T>G (p.Ile225Met) c.672T>G (p.Ile224Met) n.925T>G n.746T>G n.2064T>G | |
| 1 | g.161674017_161674037dup | CA1008429688 | FCGR2B | c.701_721dup (p.Val240_Val241insAlaAlaIleValAlaAlaVal) c.704_724dup (p.Val241_Val242insAlaAlaIleValAlaAlaVal) c.683_703dup (p.Val234_Val235insAlaAlaIleValAlaAlaVal) c.680_700dup (p.Val233_Val234insAlaAlaIleValAlaAlaVal) n.933_953dup n.754_774dup n.2072_2092dup | |
| 1 | g.161674010G>A | CA343367715 | FCGR2B | c.694G>A (p.Ala232Thr) c.697G>A (p.Ala233Thr) c.676G>A (p.Ala226Thr) c.673G>A (p.Ala225Thr) n.926G>A n.747G>A n.2065G>A | |
| 1 | g.161674010G>C | CA343367717 | FCGR2B | c.694G>C (p.Ala232Pro) c.697G>C (p.Ala233Pro) c.676G>C (p.Ala226Pro) c.673G>C (p.Ala225Pro) n.926G>C n.747G>C n.2065G>C | |
| 1 | g.161674010G>T | CA343367720 | FCGR2B | c.694G>T (p.Ala232Ser) c.697G>T (p.Ala233Ser) c.676G>T (p.Ala226Ser) c.673G>T (p.Ala225Ser) n.926G>T n.747G>T n.2065G>T | |
| 1 | g.161674011C>A | CA343367725 | FCGR2B | c.695C>A (p.Ala232Asp) c.698C>A (p.Ala233Asp) c.677C>A (p.Ala226Asp) c.674C>A (p.Ala225Asp) n.927C>A n.748C>A n.2066C>A | |
| 1 | g.161674011C>G | CA343367727 | FCGR2B | c.695C>G (p.Ala232Gly) c.698C>G (p.Ala233Gly) c.677C>G (p.Ala226Gly) c.674C>G (p.Ala225Gly) n.927C>G n.748C>G n.2066C>G | |
| 1 | g.161674011C>T | CA343367728 | FCGR2B | c.695C>T (p.Ala232Val) c.698C>T (p.Ala233Val) c.677C>T (p.Ala226Val) c.674C>T (p.Ala225Val) n.927C>T n.748C>T n.2066C>T | |
| 1 | g.161674012T>A | CA421420517 | FCGR2B | c.696T>A (p.Ala232=) c.699T>A (p.Ala233=) c.678T>A (p.Ala226=) c.675T>A (p.Ala225=) n.928T>A n.749T>A n.2067T>A | |
| 1 | g.161674012T>C | CA421420519 | FCGR2B | c.696T>C (p.Ala232=) c.699T>C (p.Ala233=) c.678T>C (p.Ala226=) c.675T>C (p.Ala225=) n.928T>C n.749T>C n.2067T>C | |
| 1 | g.161674012T>G | CA421420521 | FCGR2B | c.696T>G (p.Ala232=) c.699T>G (p.Ala233=) c.678T>G (p.Ala226=) c.675T>G (p.Ala225=) n.928T>G n.749T>G n.2067T>G | |
| 1 | g.161674013G>A | CA343367744 | FCGR2B | c.697G>A (p.Val233Ile) c.700G>A (p.Val234Ile) c.679G>A (p.Val227Ile) c.676G>A (p.Val226Ile) n.929G>A n.750G>A n.2068G>A | gnomAD |
| 1 | g.161674013G>C | CA343367732 | FCGR2B | c.697G>C (p.Val233Leu) c.700G>C (p.Val234Leu) c.679G>C (p.Val227Leu) c.676G>C (p.Val226Leu) n.929G>C n.750G>C n.2068G>C | |
| 1 | g.161674013G>T | CA343367734 | FCGR2B | c.697G>T (p.Val233Leu) c.700G>T (p.Val234Leu) c.679G>T (p.Val227Leu) c.676G>T (p.Val226Leu) n.929G>T n.750G>T n.2068G>T | |
| 1 | g.161674014T>A | CA343367748 | FCGR2B | c.698T>A (p.Val233Glu) c.701T>A (p.Val234Glu) c.680T>A (p.Val227Glu) c.677T>A (p.Val226Glu) n.930T>A n.751T>A n.2069T>A | |
| 1 | g.161674014T>C | CA343367751 | FCGR2B | c.698T>C (p.Val233Ala) c.701T>C (p.Val234Ala) c.680T>C (p.Val227Ala) c.677T>C (p.Val226Ala) n.930T>C n.751T>C n.2069T>C | |
| 1 | g.161674014T>G | CA343367753 | FCGR2B | c.698T>G (p.Val233Gly) c.701T>G (p.Val234Gly) c.680T>G (p.Val227Gly) c.677T>G (p.Val226Gly) n.930T>G n.751T>G n.2069T>G | |
| 1 | g.161674015A>C | CA421420533 | FCGR2B | c.699A>C (p.Val233=) c.702A>C (p.Val234=) c.681A>C (p.Val227=) c.678A>C (p.Val226=) n.931A>C n.752A>C n.2070A>C | |
| 1 | g.161674015A>G | CA421420532 | FCGR2B | c.699A>G (p.Val233=) c.702A>G (p.Val234=) c.681A>G (p.Val227=) c.678A>G (p.Val226=) n.931A>G n.752A>G n.2070A>G | |
| 1 | g.161674015A>T | CA421420530 | FCGR2B | c.699A>T (p.Val233=) c.702A>T (p.Val234=) c.681A>T (p.Val227=) c.678A>T (p.Val226=) n.931A>T n.752A>T n.2070A>T | |
| 1 | g.161674016G>A | CA343367758 | FCGR2B | c.700G>A (p.Ala234Thr) c.703G>A (p.Ala235Thr) c.682G>A (p.Ala228Thr) c.679G>A (p.Ala227Thr) n.932G>A n.753G>A n.2071G>A | |
| 1 | g.161674016G>C | CA343367762 | FCGR2B | c.700G>C (p.Ala234Pro) c.703G>C (p.Ala235Pro) c.682G>C (p.Ala228Pro) c.679G>C (p.Ala227Pro) n.932G>C n.753G>C n.2071G>C | |
| 1 | g.161674016G>T | CA343367764 | FCGR2B | c.700G>T (p.Ala234Ser) c.703G>T (p.Ala235Ser) c.682G>T (p.Ala228Ser) c.679G>T (p.Ala227Ser) n.932G>T n.753G>T n.2071G>T | gnomAD |
| 1 | g.161674017C>A | CA343367767 | FCGR2B | c.701C>A (p.Ala234Glu) c.704C>A (p.Ala235Glu) c.683C>A (p.Ala228Glu) c.680C>A (p.Ala227Glu) n.933C>A n.754C>A n.2072C>A | |
| 1 | g.161674017C>G | CA343367769 | FCGR2B | c.701C>G (p.Ala234Gly) c.704C>G (p.Ala235Gly) c.683C>G (p.Ala228Gly) c.680C>G (p.Ala227Gly) n.933C>G n.754C>G n.2072C>G | |
| 1 | g.161674017C>T | CA343367772 | FCGR2B | c.701C>T (p.Ala234Val) c.704C>T (p.Ala235Val) c.683C>T (p.Ala228Val) c.680C>T (p.Ala227Val) n.933C>T n.754C>T n.2072C>T | gnomAD |
| 1 | g.161674018G>A | CA421420542 | FCGR2B | c.702G>A (p.Ala234=) c.705G>A (p.Ala235=) c.684G>A (p.Ala228=) c.681G>A (p.Ala227=) n.934G>A n.755G>A n.2073G>A | gnomAD |
| 1 | g.161674018G>C | CA421420544 | FCGR2B | c.702G>C (p.Ala234=) c.705G>C (p.Ala235=) c.684G>C (p.Ala228=) c.681G>C (p.Ala227=) n.934G>C n.755G>C n.2073G>C | |
| 1 | g.161674018G>T | CA421420545 | FCGR2B | c.702G>T (p.Ala234=) c.705G>T (p.Ala235=) c.684G>T (p.Ala228=) c.681G>T (p.Ala227=) n.934G>T n.755G>T n.2073G>T | |
| 1 | g.161674019G>A | CA343367776 | FCGR2B | c.703G>A (p.Ala235Thr) c.706G>A (p.Ala236Thr) c.685G>A (p.Ala229Thr) c.682G>A (p.Ala228Thr) n.935G>A n.756G>A n.2074G>A | gnomAD |
| 1 | g.161674019G>C | CA343367778 | FCGR2B | c.703G>C (p.Ala235Pro) c.706G>C (p.Ala236Pro) c.685G>C (p.Ala229Pro) c.682G>C (p.Ala228Pro) n.935G>C n.756G>C n.2074G>C | |
| 1 | g.161674019G>T | CA343367782 | FCGR2B | c.703G>T (p.Ala235Ser) c.706G>T (p.Ala236Ser) c.685G>T (p.Ala229Ser) c.682G>T (p.Ala228Ser) n.935G>T n.756G>T n.2074G>T | |
| 1 | g.161674020C>A | CA343367794 | FCGR2B | c.704C>A (p.Ala235Asp) c.707C>A (p.Ala236Asp) c.686C>A (p.Ala229Asp) c.683C>A (p.Ala228Asp) n.936C>A n.757C>A n.2075C>A | |
| 1 | g.161674020C>G | CA343367785 | FCGR2B | c.704C>G (p.Ala235Gly) c.707C>G (p.Ala236Gly) c.686C>G (p.Ala229Gly) c.683C>G (p.Ala228Gly) n.936C>G n.757C>G n.2075C>G | |
| 1 | g.161674020C>T | CA343367792 | FCGR2B | c.704C>T (p.Ala235Val) c.707C>T (p.Ala236Val) c.686C>T (p.Ala229Val) c.683C>T (p.Ala228Val) n.936C>T n.757C>T n.2075C>T | |
| 1 | g.161674021C>A | CA421420560 | FCGR2B | c.705C>A (p.Ala235=) c.708C>A (p.Ala236=) c.687C>A (p.Ala229=) c.684C>A (p.Ala228=) n.937C>A n.758C>A n.2076C>A | |
| 1 | g.161674021C>G | CA421420557 | FCGR2B | c.705C>G (p.Ala235=) c.708C>G (p.Ala236=) c.687C>G (p.Ala229=) c.684C>G (p.Ala228=) n.937C>G n.758C>G n.2076C>G | |
| 1 | g.161674021C>T | CA421420559 | FCGR2B | c.705C>T (p.Ala235=) c.708C>T (p.Ala236=) c.687C>T (p.Ala229=) c.684C>T (p.Ala228=) n.937C>T n.758C>T n.2076C>T | |
| 1 | g.161674022A>C | CA343367798 | FCGR2B | c.706A>C (p.Ile236Leu) c.709A>C (p.Ile237Leu) c.688A>C (p.Ile230Leu) c.685A>C (p.Ile229Leu) n.938A>C n.759A>C n.2077A>C | |
| 1 | g.161674022A>G | CA343367803 | FCGR2B | c.706A>G (p.Ile236Val) c.709A>G (p.Ile237Val) c.688A>G (p.Ile230Val) c.685A>G (p.Ile229Val) n.938A>G n.759A>G n.2077A>G | |
| 1 | g.161674022A>T | CA343367801 | FCGR2B | c.706A>T (p.Ile236Phe) c.709A>T (p.Ile237Phe) c.688A>T (p.Ile230Phe) c.685A>T (p.Ile229Phe) n.938A>T n.759A>T n.2077A>T | |
| 1 | g.161674023T>A | CA343367809 | FCGR2B | c.707T>A (p.Ile236Asn) c.710T>A (p.Ile237Asn) c.689T>A (p.Ile230Asn) c.686T>A (p.Ile229Asn) n.939T>A n.760T>A n.2078T>A | |
| 1 | g.161674023T>C | CA343367812 | FCGR2B | c.707T>C (p.Ile236Thr) c.710T>C (p.Ile237Thr) c.689T>C (p.Ile230Thr) c.686T>C (p.Ile229Thr) n.939T>C n.760T>C n.2078T>C | |
| 1 | g.161674023T>G | CA343367813 | FCGR2B | c.707T>G (p.Ile236Ser) c.710T>G (p.Ile237Ser) c.689T>G (p.Ile230Ser) c.686T>G (p.Ile229Ser) n.939T>G n.760T>G n.2078T>G | |
| 1 | g.161674024T>A | CA421420572 | FCGR2B | c.708T>A (p.Ile236=) c.711T>A (p.Ile237=) c.690T>A (p.Ile230=) c.687T>A (p.Ile229=) n.940T>A n.761T>A n.2079T>A |