| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| X | g.50192595C>A | CA413188169 | AKAP4 | c.2118G>T (p.Lys706Asn) c.2091G>T (p.Lys697Asn) n.2230G>T | dbSNP |
| X | g.50192595C>G | CA413188171 | AKAP4 | c.2118G>C (p.Lys706Asn) c.2091G>C (p.Lys697Asn) n.2230G>C | |
| X | g.50192595C>T | CA516678921 | AKAP4 | c.2118G>A (p.Lys706=) c.2091G>A (p.Lys697=) n.2230G>A | |
| X | g.50192596T>A | CA413188172 | AKAP4 | c.2117A>T (p.Lys706Met) c.2090A>T (p.Lys697Met) n.2229A>T | |
| X | g.50192596T>C | CA413188174 | AKAP4 | c.2117A>G (p.Lys706Arg) c.2090A>G (p.Lys697Arg) n.2229A>G | |
| X | g.50192596T>G | CA413188176 | AKAP4 | c.2117A>C (p.Lys706Thr) c.2090A>C (p.Lys697Thr) n.2229A>C | |
| X | g.50192597T>A | CA413188178 | AKAP4 | c.2116A>T (p.Lys706Ter) c.2089A>T (p.Lys697Ter) n.2228A>T | |
| X | g.50192597T>C | CA413188180 | AKAP4 | c.2116A>G (p.Lys706Glu) c.2089A>G (p.Lys697Glu) n.2228A>G | dbSNP |
| X | g.50192597T>G | CA413188182 | AKAP4 | c.2116A>C (p.Lys706Gln) c.2089A>C (p.Lys697Gln) n.2228A>C | |
| X | g.50192598C>A | CA413188185 | AKAP4 | c.2115G>T (p.Met705Ile) c.2088G>T (p.Met696Ile) n.2227G>T | COSMIC |
| X | g.50192598C>G | CA413188186 | AKAP4 | c.2115G>C (p.Met705Ile) c.2088G>C (p.Met696Ile) n.2227G>C | |
| X | g.50192598C>T | CA413188188 | AKAP4 | c.2115G>A (p.Met705Ile) c.2088G>A (p.Met696Ile) n.2227G>A | |
| X | g.50192599A>C | CA413188194 | AKAP4 | c.2114T>G (p.Met705Arg) c.2087T>G (p.Met696Arg) n.2226T>G | |
| X | g.50192599A>G | CA413188192 | AKAP4 | c.2114T>C (p.Met705Thr) c.2087T>C (p.Met696Thr) n.2226T>C | COSMIC |
| X | g.50192599A>T | CA413188190 | AKAP4 | c.2114T>A (p.Met705Lys) c.2087T>A (p.Met696Lys) n.2226T>A | |
| X | g.50192600T>A | CA413188196 | AKAP4 | c.2113A>T (p.Met705Leu) c.2086A>T (p.Met696Leu) n.2225A>T | |
| X | g.50192600T>C | CA413188197 | AKAP4 | c.2113A>G (p.Met705Val) c.2086A>G (p.Met696Val) n.2225A>G | gnomAD v4 |
| X | g.50192600T>G | CA413188199 | AKAP4 | c.2113A>C (p.Met705Leu) c.2086A>C (p.Met696Leu) n.2225A>C | |
| X | g.50192601C>A | CA516678929 | AKAP4 | c.2112G>T (p.Val704=) c.2085G>T (p.Val695=) n.2224G>T | |
| X | g.50192601C>G | CA516678930 | AKAP4 | c.2112G>C (p.Val704=) c.2085G>C (p.Val695=) n.2224G>C | |
| X | g.50192601C>T | CA516678931 | AKAP4 | c.2112G>A (p.Val704=) c.2085G>A (p.Val695=) n.2224G>A | |
| X | g.50192602A>C | CA413188201 | AKAP4 | c.2111T>G (p.Val704Gly) c.2084T>G (p.Val695Gly) n.2223T>G | |
| X | g.50192602A>G | CA413188203 | AKAP4 | c.2111T>C (p.Val704Ala) c.2084T>C (p.Val695Ala) n.2223T>C | |
| X | g.50192602A>T | CA413188205 | AKAP4 | c.2111T>A (p.Val704Glu) c.2084T>A (p.Val695Glu) n.2223T>A | |
| X | g.50192603C>A | CA413188207 | AKAP4 | c.2110G>T (p.Val704Leu) c.2083G>T (p.Val695Leu) n.2222G>T | |
| X | g.50192603C>G | CA413188209 | AKAP4 | c.2110G>C (p.Val704Leu) c.2083G>C (p.Val695Leu) n.2222G>C | |
| X | g.50192603C>T | CA413188211 | AKAP4 | c.2110G>A (p.Val704Met) c.2083G>A (p.Val695Met) n.2222G>A | |
| X | g.50192604A>C | CA516678934 | AKAP4 | c.2109T>G (p.Ser703=) c.2082T>G (p.Ser694=) n.2221T>G | |
| X | g.50192604A>G | CA516678935 | AKAP4 | c.2109T>C (p.Ser703=) c.2082T>C (p.Ser694=) n.2221T>C | gnomAD v4 |
| X | g.50192604A>T | CA516678936 | AKAP4 | c.2109T>A (p.Ser703=) c.2082T>A (p.Ser694=) n.2221T>A | |
| X | g.50192605G>A | CA413188213 | AKAP4 | c.2108C>T (p.Ser703Phe) c.2081C>T (p.Ser694Phe) n.2220C>T | COSMIC |
| X | g.50192605G>C | CA413188214 | AKAP4 | c.2108C>G (p.Ser703Cys) c.2081C>G (p.Ser694Cys) n.2220C>G | |
| X | g.50192605G>T | CA413188215 | AKAP4 | c.2108C>A (p.Ser703Tyr) c.2081C>A (p.Ser694Tyr) n.2220C>A | |
| X | g.50192606A= | CA2428802788 | AKAP4 | c.2107T= (p.Ser703=) c.2080T= (p.Ser694=) n.2219T= | |
| X | g.50192606A>C | CA413188218 | AKAP4 | c.2107T>G (p.Ser703Ala) c.2080T>G (p.Ser694Ala) n.2219T>G | |
| X | g.50192606A>G | CA413188220 | AKAP4 | c.2107T>C (p.Ser703Pro) c.2080T>C (p.Ser694Pro) n.2219T>C | |
| X | g.50192606A>T | CA413188217 | AKAP4 | c.2107T>A (p.Ser703Thr) c.2080T>A (p.Ser694Thr) n.2219T>A | dbSNP |
| X | g.50192607T>A | CA413188224 | AKAP4 | c.2106A>T (p.Glu702Asp) c.2079A>T (p.Glu693Asp) n.2218A>T | |
| X | g.50192607T>C | CA516678939 | AKAP4 | c.2106A>G (p.Glu702=) c.2079A>G (p.Glu693=) n.2218A>G | |
| X | g.50192607T>G | CA413188222 | AKAP4 | c.2106A>C (p.Glu702Asp) c.2079A>C (p.Glu693Asp) n.2218A>C | |
| X | g.50192608T>A | CA413188226 | AKAP4 | c.2105A>T (p.Glu702Val) c.2078A>T (p.Glu693Val) n.2217A>T | |
| X | g.50192608T>C | CA413188228 | AKAP4 | c.2105A>G (p.Glu702Gly) c.2078A>G (p.Glu693Gly) n.2217A>G | |
| X | g.50192608T>G | CA413188230 | AKAP4 | c.2105A>C (p.Glu702Ala) c.2078A>C (p.Glu693Ala) n.2217A>C | |
| X | g.50192609C>A | CA413188232 | AKAP4 | c.2104G>T (p.Glu702Ter) c.2077G>T (p.Glu693Ter) n.2216G>T | |
| X | g.50192609C>G | CA413188234 | AKAP4 | c.2104G>C (p.Glu702Gln) c.2077G>C (p.Glu693Gln) n.2216G>C | |
| X | g.50192609C>T | CA413188236 | AKAP4 | c.2104G>A (p.Glu702Lys) c.2077G>A (p.Glu693Lys) n.2216G>A | |
| X | g.50192610T>A | CA516678942 | AKAP4 | c.2103A>T (p.Val701=) c.2076A>T (p.Val692=) n.2215A>T | |
| X | g.50192610T>C | CA516678944 | AKAP4 | c.2103A>G (p.Val701=) c.2076A>G (p.Val692=) n.2215A>G | |
| X | g.50192610T>G | CA516678945 | AKAP4 | c.2103A>C (p.Val701=) c.2076A>C (p.Val692=) n.2215A>C | |
| X | g.50192611A>C | CA413188238 | AKAP4 | c.2102T>G (p.Val701Gly) c.2075T>G (p.Val692Gly) n.2214T>G |