Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
7 | g.152648837_152648847delinsCAGTCGTCGAG | CA1753246884 | XRCC2 | c.470_480delinsCTCGACGACTG (p.Ser157=) c.638_648delinsCTCGACGACTG (p.Ser213=) n.660_670delinsCTCGACGACTG | |
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.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 | |
7 | g.152648847G>A | CA370198266 | XRCC2 | c.470C>T (p.Ser157Phe) c.638C>T (p.Ser213Phe) n.660C>T | |
7 | g.152648847G>C | CA370198267 | XRCC2 | c.470C>G (p.Ser157Cys) c.638C>G (p.Ser213Cys) n.660C>G | ClinVar gnomAD v4 |
7 | g.152648847G>T | CA370198268 | XRCC2 | c.470C>A (p.Ser157Tyr) c.638C>A (p.Ser213Tyr) n.660C>A | |
7 | g.152648848A>C | CA370198271 | XRCC2 | c.469T>G (p.Ser157Ala) c.637T>G (p.Ser213Ala) n.659T>G | |
7 | g.152648848A>G | CA370198270 | XRCC2 | c.469T>C (p.Ser157Pro) c.637T>C (p.Ser213Pro) n.659T>C | ClinVar gnomAD v4 |
7 | g.152648848A>T | CA370198269 | XRCC2 | c.469T>A (p.Ser157Thr) c.637T>A (p.Ser213Thr) n.659T>A | |
7 | g.152648849G>A | CA458895353 | XRCC2 | c.468C>T (p.Ala156=) c.636C>T (p.Ala212=) n.658C>T | ClinVar dbSNP |
7 | g.152648849G>C | CA169486944 | XRCC2 | c.468C>G (p.Ala156=) c.636C>G (p.Ala212=) n.658C>G | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.152648849G= | CA1753246913 | XRCC2 | c.468C= (p.Ala156=) c.636C= (p.Ala212=) n.658C= | |
7 | g.152648849G>T | CA458895354 | XRCC2 | c.468C>A (p.Ala156=) c.636C>A (p.Ala212=) n.658C>A | |
7 | g.152648850G>A | CA370198272 | XRCC2 | c.467C>T (p.Ala156Val) c.635C>T (p.Ala212Val) n.657C>T | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.152648850G>C | CA370198273 | XRCC2 | c.467C>G (p.Ala156Gly) c.635C>G (p.Ala212Gly) n.657C>G | |
7 | g.152648850G= | CA1753246916 | XRCC2 | c.467C= (p.Ala156=) c.635C= (p.Ala212=) n.657C= | |
7 | g.152648850G>T | CA4582317 | XRCC2 | c.467C>A (p.Ala156Asp) c.635C>A (p.Ala212Asp) n.657C>A | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.152648851C>A | CA370198274 | XRCC2 | c.466G>T (p.Ala156Ser) c.634G>T (p.Ala212Ser) n.656G>T | dbSNP |
7 | g.152648851C= | CA1753246918 | XRCC2 | c.466G= (p.Ala156=) c.634G= (p.Ala212=) n.656G= | |
7 | g.152648851C>G | CA370198275 | XRCC2 | c.466G>C (p.Ala156Pro) c.634G>C (p.Ala212Pro) n.656G>C | |
7 | g.152648851C>T | CA370198276 | XRCC2 | c.466G>A (p.Ala156Thr) c.634G>A (p.Ala212Thr) n.656G>A | dbSNP gnomAD v4 |
7 | g.152648852A>C | CA370198277 | XRCC2 | c.465T>G (p.His155Gln) c.633T>G (p.His211Gln) n.655T>G | |
7 | g.152648852A>G | CA458895356 | XRCC2 | c.465T>C (p.His155=) c.633T>C (p.His211=) n.655T>C | ClinVar dbSNP |
7 | g.152648852A>T | CA370198278 | XRCC2 | c.465T>A (p.His155Gln) c.633T>A (p.His211Gln) n.655T>A | |
7 | g.152648853T>A | CA370198279 | XRCC2 | c.464A>T (p.His155Leu) c.632A>T (p.His211Leu) n.654A>T | dbSNP |
7 | g.152648853T>C | CA370198280 | XRCC2 | c.464A>G (p.His155Arg) c.632A>G (p.His211Arg) n.654A>G | |
7 | g.152648853T>G | CA370198281 | XRCC2 | c.464A>C (p.His155Pro) c.632A>C (p.His211Pro) n.654A>C | dbSNP |