| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 10 | g.87967558A= | CA1926176954 | PTEN | c.*2086A= (p.=) n.3868A= | |
| 10 | g.87967558A>C | CA1926176956 | PTEN | c.*2086A>C (p.=) n.3868A>C | |
| 10 | g.87967564A= | CA1926176958 | PTEN | c.*2092A= (p.=) n.3874A= | |
| 10 | g.87967564A>G | CA211260750 | PTEN | c.*2092A>G (p.=) n.3874A>G | dbSNP |
| 10 | g.87967568T>C | CA1926176961 | PTEN | c.*2096T>C (p.=) n.3878T>C | |
| 10 | g.87967568T= | CA1926176963 | PTEN | c.*2096T= (p.=) n.3878T= | |
| 10 | g.87967569T>C | CA930911284 | PTEN | c.*2097T>C (p.=) n.3879T>C | |
| 10 | g.87967569T= | CA1926176966 | PTEN | c.*2097T= (p.=) n.3879T= | |
| 10 | g.87967574C= | CA1926176972 | PTEN | c.*2102C= (p.=) n.3884C= | |
| 10 | g.87967574C>T | CA669574992 | PTEN | c.*2102C>T (p.=) n.3884C>T | |
| 10 | g.87967575C= | CA1926176976 | PTEN | c.*2103C= (p.=) n.3885C= | |
| 10 | g.87967575C>G | CA211260753 | PTEN | c.*2103C>G (p.=) n.3885C>G | dbSNP |
| 10 | g.87967581T>G | CA211260757 | PTEN | c.*2109T>G (p.=) n.3891T>G | dbSNP gnomAD |
| 10 | g.87967581T= | CA1926176980 | PTEN | c.*2109T= (p.=) n.3891T= | |
| 10 | g.87967582G= | CA1926176984 | PTEN | c.*2110G= (p.=) n.3892G= | |
| 10 | g.87967582G>T | CA10636804 | PTEN | c.*2110G>T (p.=) n.3892G>T | ClinVar dbSNP |
| 10 | g.87967586A= | CA1926176989 | PTEN | c.*2114A= (p.=) n.3896A= | |
| 10 | g.87967586A>G | CA211260758 | PTEN | c.*2114A>G (p.=) n.3896A>G | dbSNP |
| 10 | g.87967589A= | CA1926176991 | PTEN | c.*2117A= (p.=) n.3899A= | |
| 10 | g.87967589A>G | CA1926176993 | PTEN | c.*2117A>G (p.=) n.3899A>G | |
| 10 | g.87967590_87967591delinsAC | CA1926176997 | PTEN | c.*2118_*2119delinsAC (p.=) n.3900_3901delinsAC | |
| 10 | g.87967591del | CA669574998 | PTEN | c.*2119del (p.=) n.3901del | dbSNP |
| 10 | g.87967591C= | CA1926177003 | PTEN | c.*2119C= (p.=) n.3901C= | |
| 10 | g.87967591C>T | CA1926177002 | PTEN | c.*2119C>T (p.=) n.3901C>T | |
| 10 | g.87967592T>G | CA930911290 | PTEN | c.*2120T>G (p.=) n.3902T>G | |
| 10 | g.87967592T= | CA1926177006 | PTEN | c.*2120T= (p.=) n.3902T= | |
| 10 | g.87967595A= | CA1926177008 | PTEN | c.*2123A= (p.=) n.3905A= | |
| 10 | g.87967595A>G | CA211260763 | PTEN | c.*2123A>G (p.=) n.3905A>G | dbSNP |
| 10 | g.87967598T>C | CA594924225 | PTEN | c.*2126T>C (p.=) n.3908T>C | gnomAD |
| 10 | g.87967598T= | CA1926177013 | PTEN | c.*2126T= (p.=) n.3908T= | |
| 10 | g.87967600T= | CA1926177020 | PTEN | c.*2128T= (p.=) n.3910T= | |
| 10 | g.87967601T>G | CA669575001 | PTEN | c.*2129T>G (p.=) n.3911T>G | |
| 10 | g.87967601T= | CA1926177025 | PTEN | c.*2129T= (p.=) n.3911T= | |
| 10 | g.87967601_87967602dup | CA669575002 | PTEN | c.*2129_*2130dup (p.=) n.3911_3912dup | dbSNP |
| 10 | g.87967603A= | CA1926177026 | PTEN | c.*2131A= (p.=) n.3913A= | |
| 10 | g.87967603A>C | CA1926177027 | PTEN | c.*2131A>C (p.=) n.3913A>C | |
| 10 | g.87967613T>C | CA211260769 | PTEN | c.*2141T>C (p.=) n.3923T>C | dbSNP gnomAD |
| 10 | g.87967613T= | CA1926177028 | PTEN | c.*2141T= (p.=) n.3923T= | |
| 10 | g.87967618_87967621delinsATTG | CA1926177030 | PTEN | c.*2146_*2149delinsATTG (p.=) n.3928_3931delinsATTG | |
| 10 | g.87967619T>C | CA211260788 | PTEN | c.*2147T>C (p.=) n.3929T>C | dbSNP gnomAD |
| 10 | g.87967619T= | CA1926177034 | PTEN | c.*2147T= (p.=) n.3929T= | |
| 10 | g.87967621_87967623del | CA1926177033 | PTEN | c.*2149_*2151del (p.=) n.3931_3933del | |
| 10 | g.87967621G= | CA1926177036 | PTEN | c.*2149G= (p.=) n.3931G= | |
| 10 | g.87967621G>T | CA1926177038 | PTEN | c.*2149G>T (p.=) n.3931G>T | |
| 10 | g.87967623T>C | CA930911314 | PTEN | c.*2151T>C (p.=) n.3933T>C | |
| 10 | g.87967623T>G | CA1926177042 | PTEN | c.*2151T>G (p.=) n.3933T>G | |
| 10 | g.87967623T= | CA1926177040 | PTEN | c.*2151T= (p.=) n.3933T= | |
| 10 | g.87967628G>C | CA211260794 | PTEN | c.*2156G>C (p.=) n.3938G>C | dbSNP |
| 10 | g.87967628G= | CA1926177043 | PTEN | c.*2156G= (p.=) n.3938G= | |
| 10 | g.87967632C>A | CA1926177048 | PTEN | c.*2160C>A (p.=) n.3942C>A |