Chr Mutation (hg38) CAid Gene Transcript Linkouts
7g.151186461G>ACA150541ASB10c.515C>T (p.Ala172Val)
c.470C>T (p.Ala157Val)
c.650C>T (p.Ala217Val)
ClinVar dbSNP gnomAD v4
7g.151186461G>CCA4573865ASB10c.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
7g.151186461G=CA1752544904ASB10c.515C= (p.Ala172=)
c.470C= (p.Ala157=)
c.650C= (p.Ala217=)
7g.151186461G>TCA370035882ASB10c.515C>A (p.Ala172Asp)
c.470C>A (p.Ala157Asp)
c.650C>A (p.Ala217Asp)
gnomAD v4
7g.151186462C>ACA370035885ASB10c.514G>T (p.Ala172Ser)
c.469G>T (p.Ala157Ser)
c.649G>T (p.Ala217Ser)
gnomAD v4
7g.151186462C=CA1752544909ASB10c.514G= (p.Ala172=)
c.469G= (p.Ala157=)
c.649G= (p.Ala217=)
7g.151186462C>GCA370035887ASB10c.514G>C (p.Ala172Pro)
c.469G>C (p.Ala157Pro)
c.649G>C (p.Ala217Pro)
7g.151186462C>TCA370035888ASB10c.514G>A (p.Ala172Thr)
c.469G>A (p.Ala157Thr)
c.649G>A (p.Ala217Thr)
ClinVar dbSNP gnomAD v2 gnomAD v4
7g.151186463T>ACA458881522ASB10c.513A>T (p.Gly171=)
c.468A>T (p.Gly156=)
c.648A>T (p.Gly216=)
7g.151186463T>CCA458881523ASB10c.513A>G (p.Gly171=)
c.468A>G (p.Gly156=)
c.648A>G (p.Gly216=)
dbSNP gnomAD v4
7g.151186463T>GCA458881524ASB10c.513A>C (p.Gly171=)
c.468A>C (p.Gly156=)
c.648A>C (p.Gly216=)
7g.151186463T=CA1752544913ASB10c.513A= (p.Gly171=)
c.468A= (p.Gly156=)
c.648A= (p.Gly216=)
7g.151186464C>ACA370035889ASB10c.512G>T (p.Gly171Val)
c.467G>T (p.Gly156Val)
c.647G>T (p.Gly216Val)
gnomAD v4
7g.151186464C=CA1752544917ASB10c.512G= (p.Gly171=)
c.467G= (p.Gly156=)
c.647G= (p.Gly216=)
7g.151186464C>GCA370035891ASB10c.512G>C (p.Gly171Ala)
c.467G>C (p.Gly156Ala)
c.647G>C (p.Gly216Ala)
7g.151186464C>TCA169125197ASB10c.512G>A (p.Gly171Glu)
c.467G>A (p.Gly156Glu)
c.647G>A (p.Gly216Glu)
ClinVar dbSNP gnomAD v3 gnomAD v4
7g.151186465C>ACA370035894ASB10c.511G>T (p.Gly171Ter)
c.466G>T (p.Gly156Ter)
c.646G>T (p.Gly216Ter)
dbSNP gnomAD v2 gnomAD v4
7g.151186465C=CA1752544919ASB10c.511G= (p.Gly171=)
c.466G= (p.Gly156=)
c.646G= (p.Gly216=)
7g.151186465C>GCA370035896ASB10c.511G>C (p.Gly171Arg)
c.466G>C (p.Gly156Arg)
c.646G>C (p.Gly216Arg)
7g.151186465C>TCA4573866ASB10c.511G>A (p.Gly171Arg)
c.466G>A (p.Gly156Arg)
c.646G>A (p.Gly216Arg)
dbSNP ExAC gnomAD v2 gnomAD v4
7g.151186466T>ACA458881527ASB10c.510A>T (p.Ala170=)
c.465A>T (p.Ala155=)
c.645A>T (p.Ala215=)
7g.151186466T>CCA458881529ASB10c.510A>G (p.Ala170=)
c.465A>G (p.Ala155=)
c.645A>G (p.Ala215=)
gnomAD v4
7g.151186466T>GCA458881530ASB10c.510A>C (p.Ala170=)
c.465A>C (p.Ala155=)
c.645A>C (p.Ala215=)
7g.151186467G>ACA370035899ASB10c.509C>T (p.Ala170Val)
c.464C>T (p.Ala155Val)
c.644C>T (p.Ala215Val)
gnomAD v4
7g.151186467G>CCA370035901ASB10c.509C>G (p.Ala170Gly)
c.464C>G (p.Ala155Gly)
c.644C>G (p.Ala215Gly)
7g.151186467G>TCA370035903ASB10c.509C>A (p.Ala170Glu)
c.464C>A (p.Ala155Glu)
c.644C>A (p.Ala215Glu)
7g.151186468C>ACA370035909ASB10c.508G>T (p.Ala170Ser)
c.463G>T (p.Ala155Ser)
c.643G>T (p.Ala215Ser)
gnomAD v4
7g.151186468C>GCA370035907ASB10c.508G>C (p.Ala170Pro)
c.463G>C (p.Ala155Pro)
c.643G>C (p.Ala215Pro)
7g.151186468C>TCA370035905ASB10c.508G>A (p.Ala170Thr)
c.463G>A (p.Ala155Thr)
c.643G>A (p.Ala215Thr)
7g.151186469C>ACA458881532ASB10c.507G>T (p.Val169=)
c.462G>T (p.Val154=)
c.642G>T (p.Val214=)
gnomAD v4
7g.151186469C>GCA458881533ASB10c.507G>C (p.Val169=)
c.462G>C (p.Val154=)
c.642G>C (p.Val214=)
7g.151186469C>TCA458881534ASB10c.507G>A (p.Val169=)
c.462G>A (p.Val154=)
c.642G>A (p.Val214=)
7g.151186470A>CCA370035910ASB10c.506T>G (p.Val169Gly)
c.461T>G (p.Val154Gly)
c.641T>G (p.Val214Gly)
7g.151186470A>GCA370035912ASB10c.506T>C (p.Val169Ala)
c.461T>C (p.Val154Ala)
c.641T>C (p.Val214Ala)
7g.151186470A>TCA370035914ASB10c.506T>A (p.Val169Glu)
c.461T>A (p.Val154Glu)
c.641T>A (p.Val214Glu)
7g.151186471C>ACA370035916ASB10c.505G>T (p.Val169Leu)
c.460G>T (p.Val154Leu)
c.640G>T (p.Val214Leu)
gnomAD v4
7g.151186471C=CA1752544921ASB10c.505G= (p.Val169=)
c.460G= (p.Val154=)
c.640G= (p.Val214=)
7g.151186471C>GCA370035917ASB10c.505G>C (p.Val169Leu)
c.460G>C (p.Val154Leu)
c.640G>C (p.Val214Leu)
gnomAD v4
7g.151186471C>TCA169125236ASB10c.505G>A (p.Val169Met)
c.460G>A (p.Val154Met)
c.640G>A (p.Val214Met)
dbSNP gnomAD v2 gnomAD v4
7g.151186472C>ACA458881537ASB10c.504G>T (p.Leu168=)
c.459G>T (p.Leu153=)
c.639G>T (p.Leu213=)
gnomAD v4
7g.151186472C>GCA458881539ASB10c.504G>C (p.Leu168=)
c.459G>C (p.Leu153=)
c.639G>C (p.Leu213=)
7g.151186472C>TCA458881538ASB10c.504G>A (p.Leu168=)
c.459G>A (p.Leu153=)
c.639G>A (p.Leu213=)
7g.151186473A>CCA370035920ASB10c.503T>G (p.Leu168Arg)
c.458T>G (p.Leu153Arg)
c.638T>G (p.Leu213Arg)
7g.151186473A>GCA370035922ASB10c.503T>C (p.Leu168Pro)
c.458T>C (p.Leu153Pro)
c.638T>C (p.Leu213Pro)
7g.151186473A>TCA370035924ASB10c.503T>A (p.Leu168Gln)
c.458T>A (p.Leu153Gln)
c.638T>A (p.Leu213Gln)
7g.151186474G>ACA458881540ASB10c.502C>T (p.Leu168=)
c.457C>T (p.Leu153=)
c.637C>T (p.Leu213=)
gnomAD v4
7g.151186474G>CCA370035926ASB10c.502C>G (p.Leu168Val)
c.457C>G (p.Leu153Val)
c.637C>G (p.Leu213Val)
7g.151186474G>TCA370035927ASB10c.502C>A (p.Leu168Met)
c.457C>A (p.Leu153Met)
c.637C>A (p.Leu213Met)
gnomAD v4
7g.151186475C>ACA458881541ASB10c.501G>T (p.Leu167=)
c.456G>T (p.Leu152=)
c.636G>T (p.Leu212=)
gnomAD v4
7g.151186475C=CA1752544925ASB10c.501G= (p.Leu167=)
c.456G= (p.Leu152=)
c.636G= (p.Leu212=)

Number of alleles fetched