Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
7 | g.152648837_152648838del | CA16618428 | XRCC2 | c.483_484del (p.Cys161Ter) c.651_652del (p.Cys217Ter) n.673_674del | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.152648838_152648839insACCAAACACACCCAACACA | CA2778474372 | XRCC2 | c.483_484insTGGGTGTGTTTGGTTGTGT (p.Asp162TrpfsTer7) c.651_652insTGGGTGTGTTTGGTTGTGT (p.Asp218TrpfsTer7) n.673_674insTGGGTGTGTTTGGTTGTGT | |
7 | g.152648835C>A | CA370198249 | XRCC2 | c.482G>T (p.Cys161Phe) c.650G>T (p.Cys217Phe) n.672G>T | |
7 | g.152648835C= | CA1753246879 | XRCC2 | c.482G= (p.Cys161=) c.650G= (p.Cys217=) n.672G= | |
7 | g.152648835C>G | CA370198250 | XRCC2 | c.482G>C (p.Cys161Ser) c.650G>C (p.Cys217Ser) n.672G>C | dbSNP |
7 | g.152648835C>T | CA10584276 | XRCC2 | c.482G>A (p.Cys161Tyr) c.650G>A (p.Cys217Tyr) n.672G>A | ClinVar dbSNP |
7 | g.152648836A= | CA1753246882 | XRCC2 | c.481T= (p.Cys161=) c.649T= (p.Cys217=) n.671T= | |
7 | g.152648836A>C | CA370198251 | XRCC2 | c.481T>G (p.Cys161Gly) c.649T>G (p.Cys217Gly) n.671T>G | |
7 | g.152648836A>G | CA370198252 | XRCC2 | c.481T>C (p.Cys161Arg) c.649T>C (p.Cys217Arg) n.671T>C | dbSNP |
7 | g.152648836A>T | CA370198253 | XRCC2 | c.481T>A (p.Cys161Ser) c.649T>A (p.Cys217Ser) n.671T>A | gnomAD v4 |
7 | g.152648837C>A | CA458895330 | XRCC2 | c.480G>T (p.Leu160=) c.648G>T (p.Leu216=) n.670G>T | ClinVar |
7 | g.152648837C>G | CA458895331 | XRCC2 | c.480G>C (p.Leu160=) c.648G>C (p.Leu216=) n.670G>C | |
7 | g.152648837C>T | CA458895332 | XRCC2 | c.480G>A (p.Leu160=) c.648G>A (p.Leu216=) n.670G>A | ClinVar gnomAD v4 |
7 | g.152648837_152648847delinsCAGTCGTCGAG | CA1753246884 | XRCC2 | c.470_480delinsCTCGACGACTG (p.Ser157=) c.638_648delinsCTCGACGACTG (p.Ser213=) n.660_670delinsCTCGACGACTG | |
7 | g.152648838A= | CA1753246887 | XRCC2 | c.479T= (p.Leu160=) c.647T= (p.Leu216=) n.669T= | |
7 | g.152648838A>C | CA370198254 | XRCC2 | c.479T>G (p.Leu160Arg) c.647T>G (p.Leu216Arg) n.669T>G | |
7 | g.152648838A>G | CA370198255 | XRCC2 | c.479T>C (p.Leu160Pro) c.647T>C (p.Leu216Pro) n.669T>C | ClinVar dbSNP gnomAD v4 |
7 | g.152648838A>T | CA370198256 | XRCC2 | c.479T>A (p.Leu160Gln) c.647T>A (p.Leu216Gln) n.669T>A | |
7 | g.152648840_152648849del | CA579080840 | XRCC2 | c.470_479del (p.Ser157CysfsTer6) c.638_647del (p.Ser213CysfsTer6) n.660_669del | dbSNP gnomAD v2 gnomAD v4 |
7 | g.152648839G>A | CA458895333 | XRCC2 | c.478C>T (p.Leu160=) c.646C>T (p.Leu216=) n.668C>T | |
7 | g.152648839G>C | CA370198257 | XRCC2 | c.478C>G (p.Leu160Val) c.646C>G (p.Leu216Val) n.668C>G | dbSNP |
7 | g.152648839G>T | CA370198258 | XRCC2 | c.478C>A (p.Leu160Met) c.646C>A (p.Leu216Met) n.668C>A | |
7 | g.152648840T>A | CA458895335 | XRCC2 | c.477A>T (p.Arg159=) c.645A>T (p.Arg215=) n.667A>T | |
7 | g.152648840T>C | CA458895336 | XRCC2 | c.477A>G (p.Arg159=) c.645A>G (p.Arg215=) n.667A>G | gnomAD v4 |
7 | g.152648840T>G | CA458895337 | XRCC2 | c.477A>C (p.Arg159=) c.645A>C (p.Arg215=) n.667A>C | ClinVar dbSNP gnomAD v2 gnomAD v4 |
7 | g.152648840T= | CA1753246889 | XRCC2 | c.477A= (p.Arg159=) c.645A= (p.Arg215=) n.667A= | |
7 | g.152648841C>A | CA370198260 | XRCC2 | c.476G>T (p.Arg159Leu) c.644G>T (p.Arg215Leu) n.666G>T | gnomAD v4 |
7 | g.152648841C= | CA1753246892 | XRCC2 | c.476G= (p.Arg159=) c.644G= (p.Arg215=) n.666G= | |
7 | g.152648841C>G | CA370198259 | XRCC2 | c.476G>C (p.Arg159Pro) c.644G>C (p.Arg215Pro) n.666G>C | |
7 | g.152648841C>T | CA4582316 | XRCC2 | c.476G>A (p.Arg159Gln) c.644G>A (p.Arg215Gln) n.666G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
7 | g.152648842G>A | CA128903 | XRCC2 | c.475C>T (p.Arg159Ter) c.643C>T (p.Arg215Ter) n.665C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.152648842G>C | CA370198261 | XRCC2 | c.475C>G (p.Arg159Gly) c.643C>G (p.Arg215Gly) n.665C>G | |
7 | g.152648842G= | CA1753246897 | XRCC2 | c.475C= (p.Arg159=) c.643C= (p.Arg215=) n.665C= | |
7 | g.152648842G>T | CA458895338 | XRCC2 | c.475C>A (p.Arg159=) c.643C>A (p.Arg215=) n.665C>A | gnomAD v4 |
7 | g.152648843T>A | CA458895340 | XRCC2 | c.474A>T (p.Arg158=) c.642A>T (p.Arg214=) n.664A>T | dbSNP |
7 | g.152648843T>C | CA458895342 | XRCC2 | c.474A>G (p.Arg158=) c.642A>G (p.Arg214=) n.664A>G | |
7 | g.152648843T>G | CA458895341 | XRCC2 | c.474A>C (p.Arg158=) c.642A>C (p.Arg214=) n.664A>C | |
7 | g.152648844C>A | CA370198262 | XRCC2 | c.473G>T (p.Arg158Leu) c.641G>T (p.Arg214Leu) n.663G>T | dbSNP |
7 | g.152648844C= | CA1753246902 | XRCC2 | c.473G= (p.Arg158=) c.641G= (p.Arg214=) n.663G= | |
7 | g.152648844C>G | CA370198263 | XRCC2 | c.473G>C (p.Arg158Pro) c.641G>C (p.Arg214Pro) n.663G>C | dbSNP gnomAD v4 |
7 | g.152648844C>T | CA288143 | XRCC2 | c.473G>A (p.Arg158Gln) c.641G>A (p.Arg214Gln) n.663G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.152648844_152648846delinsCGA | CA1753246904 | XRCC2 | c.471_473delinsTCG (p.Ser157=) c.639_641delinsTCG (p.Ser213=) n.661_663delinsTCG | |
7 | g.152648845G>A | CA370198264 | XRCC2 | c.472C>T (p.Arg158Ter) c.640C>T (p.Arg214Ter) n.662C>T | ClinVar dbSNP gnomAD v3 gnomAD v4 |
7 | g.152648845G>C | CA370198265 | XRCC2 | c.472C>G (p.Arg158Gly) c.640C>G (p.Arg214Gly) n.662C>G | |
7 | g.152648845G= | CA1753246910 | XRCC2 | c.472C= (p.Arg158=) c.640C= (p.Arg214=) n.662C= | |
7 | g.152648845G>T | CA458895345 | XRCC2 | c.472C>A (p.Arg158=) c.640C>A (p.Arg214=) n.662C>A | |
7 | g.152648848_152648849del | CA1753246908 | XRCC2 | c.471_472del (p.Arg158ThrfsTer4) c.639_640del (p.Arg214ThrfsTer4) n.661_662del | dbSNP |
7 | g.152648846A>C | CA458895347 | XRCC2 | c.471T>G (p.Ser157=) c.639T>G (p.Ser213=) n.661T>G | |
7 | g.152648846A>G | CA458895348 | XRCC2 | c.471T>C (p.Ser157=) c.639T>C (p.Ser213=) n.661T>C | |
7 | g.152648846A>T | CA458895349 | XRCC2 | c.471T>A (p.Ser157=) c.639T>A (p.Ser213=) n.661T>A |