Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
7 | g.151186461G>A | CA150541 | ASB10 | c.515C>T (p.Ala172Val) c.470C>T (p.Ala157Val) c.650C>T (p.Ala217Val) | ClinVar dbSNP gnomAD v4 |
7 | g.151186461G>C | CA4573865 | ASB10 | c.515C>G (p.Ala172Gly) c.470C>G (p.Ala157Gly) c.650C>G (p.Ala217Gly) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC COSMIC COSMIC |
7 | g.151186461G= | CA1752544904 | ASB10 | c.515C= (p.Ala172=) c.470C= (p.Ala157=) c.650C= (p.Ala217=) | |
7 | g.151186461G>T | CA370035882 | ASB10 | c.515C>A (p.Ala172Asp) c.470C>A (p.Ala157Asp) c.650C>A (p.Ala217Asp) | gnomAD v4 |
7 | g.151186462C>A | CA370035885 | ASB10 | c.514G>T (p.Ala172Ser) c.469G>T (p.Ala157Ser) c.649G>T (p.Ala217Ser) | gnomAD v4 |
7 | g.151186462C= | CA1752544909 | ASB10 | c.514G= (p.Ala172=) c.469G= (p.Ala157=) c.649G= (p.Ala217=) | |
7 | g.151186462C>G | CA370035887 | ASB10 | c.514G>C (p.Ala172Pro) c.469G>C (p.Ala157Pro) c.649G>C (p.Ala217Pro) | |
7 | g.151186462C>T | CA370035888 | ASB10 | c.514G>A (p.Ala172Thr) c.469G>A (p.Ala157Thr) c.649G>A (p.Ala217Thr) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
7 | g.151186463T>A | CA458881522 | ASB10 | c.513A>T (p.Gly171=) c.468A>T (p.Gly156=) c.648A>T (p.Gly216=) | |
7 | g.151186463T>C | CA458881523 | ASB10 | c.513A>G (p.Gly171=) c.468A>G (p.Gly156=) c.648A>G (p.Gly216=) | dbSNP gnomAD v4 |
7 | g.151186463T>G | CA458881524 | ASB10 | c.513A>C (p.Gly171=) c.468A>C (p.Gly156=) c.648A>C (p.Gly216=) | |
7 | g.151186463T= | CA1752544913 | ASB10 | c.513A= (p.Gly171=) c.468A= (p.Gly156=) c.648A= (p.Gly216=) | |
7 | g.151186464C>A | CA370035889 | ASB10 | c.512G>T (p.Gly171Val) c.467G>T (p.Gly156Val) c.647G>T (p.Gly216Val) | gnomAD v4 |
7 | g.151186464C= | CA1752544917 | ASB10 | c.512G= (p.Gly171=) c.467G= (p.Gly156=) c.647G= (p.Gly216=) | |
7 | g.151186464C>G | CA370035891 | ASB10 | c.512G>C (p.Gly171Ala) c.467G>C (p.Gly156Ala) c.647G>C (p.Gly216Ala) | |
7 | g.151186464C>T | CA169125197 | ASB10 | c.512G>A (p.Gly171Glu) c.467G>A (p.Gly156Glu) c.647G>A (p.Gly216Glu) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
7 | g.151186465C>A | CA370035894 | ASB10 | c.511G>T (p.Gly171Ter) c.466G>T (p.Gly156Ter) c.646G>T (p.Gly216Ter) | dbSNP gnomAD v2 gnomAD v4 |
7 | g.151186465C= | CA1752544919 | ASB10 | c.511G= (p.Gly171=) c.466G= (p.Gly156=) c.646G= (p.Gly216=) | |
7 | g.151186465C>G | CA370035896 | ASB10 | c.511G>C (p.Gly171Arg) c.466G>C (p.Gly156Arg) c.646G>C (p.Gly216Arg) | |
7 | g.151186465C>T | CA4573866 | ASB10 | c.511G>A (p.Gly171Arg) c.466G>A (p.Gly156Arg) c.646G>A (p.Gly216Arg) | dbSNP ExAC gnomAD v2 gnomAD v4 |
7 | g.151186466T>A | CA458881527 | ASB10 | c.510A>T (p.Ala170=) c.465A>T (p.Ala155=) c.645A>T (p.Ala215=) | |
7 | g.151186466T>C | CA458881529 | ASB10 | c.510A>G (p.Ala170=) c.465A>G (p.Ala155=) c.645A>G (p.Ala215=) | gnomAD v4 |
7 | g.151186466T>G | CA458881530 | ASB10 | c.510A>C (p.Ala170=) c.465A>C (p.Ala155=) c.645A>C (p.Ala215=) | |
7 | g.151186467G>A | CA370035899 | ASB10 | c.509C>T (p.Ala170Val) c.464C>T (p.Ala155Val) c.644C>T (p.Ala215Val) | gnomAD v4 |
7 | g.151186467G>C | CA370035901 | ASB10 | c.509C>G (p.Ala170Gly) c.464C>G (p.Ala155Gly) c.644C>G (p.Ala215Gly) | |
7 | g.151186467G>T | CA370035903 | ASB10 | c.509C>A (p.Ala170Glu) c.464C>A (p.Ala155Glu) c.644C>A (p.Ala215Glu) | |
7 | g.151186468C>A | CA370035909 | ASB10 | c.508G>T (p.Ala170Ser) c.463G>T (p.Ala155Ser) c.643G>T (p.Ala215Ser) | gnomAD v4 |
7 | g.151186468C>G | CA370035907 | ASB10 | c.508G>C (p.Ala170Pro) c.463G>C (p.Ala155Pro) c.643G>C (p.Ala215Pro) | |
7 | g.151186468C>T | CA370035905 | ASB10 | c.508G>A (p.Ala170Thr) c.463G>A (p.Ala155Thr) c.643G>A (p.Ala215Thr) | |
7 | g.151186469C>A | CA458881532 | ASB10 | c.507G>T (p.Val169=) c.462G>T (p.Val154=) c.642G>T (p.Val214=) | gnomAD v4 |
7 | g.151186469C>G | CA458881533 | ASB10 | c.507G>C (p.Val169=) c.462G>C (p.Val154=) c.642G>C (p.Val214=) | |
7 | g.151186469C>T | CA458881534 | ASB10 | c.507G>A (p.Val169=) c.462G>A (p.Val154=) c.642G>A (p.Val214=) | |
7 | g.151186470A>C | CA370035910 | ASB10 | c.506T>G (p.Val169Gly) c.461T>G (p.Val154Gly) c.641T>G (p.Val214Gly) | |
7 | g.151186470A>G | CA370035912 | ASB10 | c.506T>C (p.Val169Ala) c.461T>C (p.Val154Ala) c.641T>C (p.Val214Ala) | |
7 | g.151186470A>T | CA370035914 | ASB10 | c.506T>A (p.Val169Glu) c.461T>A (p.Val154Glu) c.641T>A (p.Val214Glu) | |
7 | g.151186471C>A | CA370035916 | ASB10 | c.505G>T (p.Val169Leu) c.460G>T (p.Val154Leu) c.640G>T (p.Val214Leu) | gnomAD v4 |
7 | g.151186471C= | CA1752544921 | ASB10 | c.505G= (p.Val169=) c.460G= (p.Val154=) c.640G= (p.Val214=) | |
7 | g.151186471C>G | CA370035917 | ASB10 | c.505G>C (p.Val169Leu) c.460G>C (p.Val154Leu) c.640G>C (p.Val214Leu) | gnomAD v4 |
7 | g.151186471C>T | CA169125236 | ASB10 | c.505G>A (p.Val169Met) c.460G>A (p.Val154Met) c.640G>A (p.Val214Met) | dbSNP gnomAD v2 gnomAD v4 |
7 | g.151186472C>A | CA458881537 | ASB10 | c.504G>T (p.Leu168=) c.459G>T (p.Leu153=) c.639G>T (p.Leu213=) | gnomAD v4 |
7 | g.151186472C>G | CA458881539 | ASB10 | c.504G>C (p.Leu168=) c.459G>C (p.Leu153=) c.639G>C (p.Leu213=) | |
7 | g.151186472C>T | CA458881538 | ASB10 | c.504G>A (p.Leu168=) c.459G>A (p.Leu153=) c.639G>A (p.Leu213=) | |
7 | g.151186473A>C | CA370035920 | ASB10 | c.503T>G (p.Leu168Arg) c.458T>G (p.Leu153Arg) c.638T>G (p.Leu213Arg) | |
7 | g.151186473A>G | CA370035922 | ASB10 | c.503T>C (p.Leu168Pro) c.458T>C (p.Leu153Pro) c.638T>C (p.Leu213Pro) | |
7 | g.151186473A>T | CA370035924 | ASB10 | c.503T>A (p.Leu168Gln) c.458T>A (p.Leu153Gln) c.638T>A (p.Leu213Gln) | |
7 | g.151186474G>A | CA458881540 | ASB10 | c.502C>T (p.Leu168=) c.457C>T (p.Leu153=) c.637C>T (p.Leu213=) | gnomAD v4 |
7 | g.151186474G>C | CA370035926 | ASB10 | c.502C>G (p.Leu168Val) c.457C>G (p.Leu153Val) c.637C>G (p.Leu213Val) | |
7 | g.151186474G>T | CA370035927 | ASB10 | c.502C>A (p.Leu168Met) c.457C>A (p.Leu153Met) c.637C>A (p.Leu213Met) | gnomAD v4 |
7 | g.151186475C>A | CA458881541 | ASB10 | c.501G>T (p.Leu167=) c.456G>T (p.Leu152=) c.636G>T (p.Leu212=) | gnomAD v4 |
7 | g.151186475C= | CA1752544925 | ASB10 | c.501G= (p.Leu167=) c.456G= (p.Leu152=) c.636G= (p.Leu212=) |