| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 10 | g.87967657C= | CA1926177102 | PTEN | c.*2185C= (p.=) n.3967C= | |
| 10 | g.87967657C>T | CA10636805 | PTEN | c.*2185C>T (p.=) n.3967C>T | ClinVar dbSNP gnomAD |
| 10 | g.87967659T>C | CA1926177109 | PTEN | c.*2187T>C (p.=) n.3969T>C | |
| 10 | g.87967659T= | CA1926177108 | PTEN | c.*2187T= (p.=) n.3969T= | |
| 10 | g.87967660A= | CA1926177111 | PTEN | c.*2188A= (p.=) n.3970A= | |
| 10 | g.87967660A>G | CA211260853 | PTEN | c.*2188A>G (p.=) n.3970A>G | dbSNP |
| 10 | g.87967661A= | CA1926177116 | PTEN | c.*2189A= (p.=) n.3971A= | |
| 10 | g.87967661A>G | CA594924230 | PTEN | c.*2189A>G (p.=) n.3971A>G | gnomAD |
| 10 | g.87967663T>G | CA1926177120 | PTEN | c.*2191T>G (p.=) n.3973T>G | |
| 10 | g.87967663T= | CA1926177117 | PTEN | c.*2191T= (p.=) n.3973T= | |
| 10 | g.87967664T>C | CA669575041 | PTEN | c.*2192T>C (p.=) n.3974T>C | |
| 10 | g.87967664T= | CA1926177121 | PTEN | c.*2192T= (p.=) n.3974T= | |
| 10 | g.87967666_87967669delinsATTG | CA1926177122 | PTEN | c.*2194_*2197delinsATTG (p.=) n.3976_3979delinsATTG | |
| 10 | g.87967669_87967671del | CA211260859 | PTEN | c.*2197_*2199del (p.=) n.3979_3981del | dbSNP |
| 10 | g.87967671T>A | CA594924231 | PTEN | c.*2199T>A (p.=) n.3981T>A | gnomAD |
| 10 | g.87967671T= | CA1926177123 | PTEN | c.*2199T= (p.=) n.3981T= | |
| 10 | g.87967672C>A | CA10636809 | PTEN | c.*2200C>A (p.=) n.3982C>A | ClinVar dbSNP |
| 10 | g.87967672C= | CA1926177124 | PTEN | c.*2200C= (p.=) n.3982C= | |
| 10 | g.87967675A= | CA1926177125 | PTEN | c.*2203A= (p.=) n.3985A= | |
| 10 | g.87967675A>G | CA10636815 | PTEN | c.*2203A>G (p.=) n.3985A>G | ClinVar dbSNP dbSNP gnomAD |
| 10 | g.87967676T>A | CA10636816 | PTEN | c.*2204T>A (p.=) n.3986T>A | ClinVar dbSNP |
| 10 | g.87967676T= | CA1926177127 | PTEN | c.*2204T= (p.=) n.3986T= | |
| 10 | g.87967677A= | CA1926177128 | PTEN | c.*2205A= (p.=) n.3987A= | |
| 10 | g.87967677A>G | CA211260872 | PTEN | c.*2205A>G (p.=) n.3987A>G | dbSNP |
| 10 | g.87967679G>A | CA1926177131 | PTEN | c.*2207G>A (p.=) n.3989G>A | |
| 10 | g.87967679G= | CA1926177130 | PTEN | c.*2207G= (p.=) n.3989G= | |
| 10 | g.87967684A= | CA1926177132 | PTEN | c.*2212A= (p.=) n.3994A= | |
| 10 | g.87967684A>G | CA1926177133 | PTEN | c.*2212A>G (p.=) n.3994A>G | |
| 10 | g.87967688A= | CA1926177135 | PTEN | c.*2216A= (p.=) n.3998A= | |
| 10 | g.87967688A>G | CA930911355 | PTEN | c.*2216A>G (p.=) n.3998A>G | |
| 10 | g.87967689G>A | CA1926177137 | PTEN | c.*2217G>A (p.=) n.3999G>A | |
| 10 | g.87967689G= | CA1926177136 | PTEN | c.*2217G= (p.=) n.3999G= | |
| 10 | g.87967691G= | CA1926177139 | PTEN | c.*2219G= (p.=) n.4001G= | |
| 10 | g.87967691G>T | CA669575079 | PTEN | c.*2219G>T (p.=) n.4001G>T | |
| 10 | g.87967692C= | CA1926177140 | PTEN | c.*2220C= (p.=) n.4002C= | |
| 10 | g.87967692C>T | CA930911356 | PTEN | c.*2220C>T (p.=) n.4002C>T | |
| 10 | g.87967693C= | CA1926177142 | PTEN | c.*2221C= (p.=) n.4003C= | |
| 10 | g.87967693C>T | CA930911357 | PTEN | c.*2221C>T (p.=) n.4003C>T | |
| 10 | g.87967695G= | CA1926177144 | PTEN | c.*2223G= (p.=) n.4005G= | |
| 10 | g.87967695G>T | CA211260873 | PTEN | c.*2223G>T (p.=) n.4005G>T | dbSNP gnomAD |
| 10 | g.87967696G>C | CA1926177160 | PTEN | c.*2224G>C (p.=) n.4006G>C | |
| 10 | g.87967696G= | CA1926177158 | PTEN | c.*2224G= (p.=) n.4006G= | |
| 10 | g.87967696G>T | CA669575082 | PTEN | c.*2224G>T (p.=) n.4006G>T | |
| 10 | g.87967699A= | CA1926177162 | PTEN | c.*2227A= (p.=) n.4009A= | |
| 10 | g.87967699A>G | CA211260879 | PTEN | c.*2227A>G (p.=) n.4009A>G | dbSNP |
| 10 | g.87967700T>C | CA1926177166 | PTEN | c.*2228T>C (p.=) n.4010T>C | |
| 10 | g.87967700T= | CA1926177164 | PTEN | c.*2228T= (p.=) n.4010T= | |
| 10 | g.87967704T>C | CA1926177169 | PTEN | c.*2232T>C (p.=) n.4014T>C | |
| 10 | g.87967704T= | CA1926177167 | PTEN | c.*2232T= (p.=) n.4014T= | |
| 10 | g.87967705A= | CA1926177171 | PTEN | c.*2233A= (p.=) n.4015A= |