Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
1 | g.16132227del | CA2643574136 | EPHA2 | c.2165del (p.Gly722AlafsTer6) c.2003del (p.Gly668AlafsTer6) | gnomAD v4 |
1 | g.16132227C>A | CA338622614 | EPHA2 | c.2162G>T (p.Arg721Leu) c.2000G>T (p.Arg667Leu) | |
1 | g.16132227C= | CA1141534616 | EPHA2 | c.2162G= (p.Arg721=) c.2000G= (p.Arg667=) | |
1 | g.16132227C>G | CA338622616 | EPHA2 | c.2162G>C (p.Arg721Pro) c.2000G>C (p.Arg667Pro) | gnomAD v4 |
1 | g.16132227C>T | CA122982 | EPHA2 | c.2162G>A (p.Arg721Gln) c.2000G>A (p.Arg667Gln) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.16132228G>A | CA624902 | EPHA2 | c.2161C>T (p.Arg721Trp) c.1999C>T (p.Arg667Trp) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
1 | g.16132228G>C | CA338622622 | EPHA2 | c.2161C>G (p.Arg721Gly) c.1999C>G (p.Arg667Gly) | dbSNP |
1 | g.16132228G= | CA1144149323 | EPHA2 | c.2161C= (p.Arg721=) c.1999C= (p.Arg667=) | |
1 | g.16132228G>T | CA416385667 | EPHA2 | c.2161C>A (p.Arg721=) c.1999C>A (p.Arg667=) | |
1 | g.16132229C>A | CA416385668 | EPHA2 | c.2160G>T (p.Leu720=) c.1998G>T (p.Leu666=) | |
1 | g.16132229C>G | CA416385670 | EPHA2 | c.2160G>C (p.Leu720=) c.1998G>C (p.Leu666=) | |
1 | g.16132229C>T | CA416385671 | EPHA2 | c.2160G>A (p.Leu720=) c.1998G>A (p.Leu666=) | dbSNP |
1 | g.16132230A>C | CA338622625 | EPHA2 | c.2159T>G (p.Leu720Arg) c.1997T>G (p.Leu666Arg) | |
1 | g.16132230A>G | CA338622627 | EPHA2 | c.2159T>C (p.Leu720Pro) c.1997T>C (p.Leu666Pro) | |
1 | g.16132230A>T | CA338622628 | EPHA2 | c.2159T>A (p.Leu720Gln) c.1997T>A (p.Leu666Gln) | |
1 | g.16132231G>A | CA416385674 | EPHA2 | c.2158C>T (p.Leu720=) c.1996C>T (p.Leu666=) | dbSNP |
1 | g.16132231G>C | CA338622629 | EPHA2 | c.2158C>G (p.Leu720Val) c.1996C>G (p.Leu666Val) | dbSNP |
1 | g.16132231G>T | CA338622630 | EPHA2 | c.2158C>A (p.Leu720Met) c.1996C>A (p.Leu666Met) | |
1 | g.16132232C>A | CA338622631 | EPHA2 | c.2157G>T (p.Met719Ile) c.1995G>T (p.Met665Ile) | |
1 | g.16132232C>G | CA338622632 | EPHA2 | c.2157G>C (p.Met719Ile) c.1995G>C (p.Met665Ile) | |
1 | g.16132232C>T | CA338622635 | EPHA2 | c.2157G>A (p.Met719Ile) c.1995G>A (p.Met665Ile) | dbSNP gnomAD v4 |
1 | g.16132233A>C | CA338622641 | EPHA2 | c.2156T>G (p.Met719Arg) c.1994T>G (p.Met665Arg) | |
1 | g.16132233A>G | CA338622638 | EPHA2 | c.2156T>C (p.Met719Thr) c.1994T>C (p.Met665Thr) | |
1 | g.16132233A>T | CA338622639 | EPHA2 | c.2156T>A (p.Met719Lys) c.1994T>A (p.Met665Lys) | |
1 | g.16132234T>A | CA338622642 | EPHA2 | c.2155A>T (p.Met719Leu) c.1993A>T (p.Met665Leu) | |
1 | g.16132234T>C | CA624903 | EPHA2 | c.2155A>G (p.Met719Val) c.1993A>G (p.Met665Val) | dbSNP ExAC gnomAD v2 gnomAD v4 |
1 | g.16132234T>G | CA338622647 | EPHA2 | c.2155A>C (p.Met719Leu) c.1993A>C (p.Met665Leu) | gnomAD v4 |
1 | g.16132234T= | CA1155650212 | EPHA2 | c.2155A= (p.Met719=) c.1993A= (p.Met665=) | |
1 | g.16132235G>A | CA416385684 | EPHA2 | c.2154C>T (p.Gly718=) c.1992C>T (p.Gly664=) | dbSNP gnomAD v4 |
1 | g.16132235G>C | CA416385686 | EPHA2 | c.2154C>G (p.Gly718=) c.1992C>G (p.Gly664=) | dbSNP |
1 | g.16132235G>T | CA416385687 | EPHA2 | c.2154C>A (p.Gly718=) c.1992C>A (p.Gly664=) | |
1 | g.16132236C>A | CA338622650 | EPHA2 | c.2153G>T (p.Gly718Val) c.1991G>T (p.Gly664Val) | |
1 | g.16132236C>G | CA338622653 | EPHA2 | c.2153G>C (p.Gly718Ala) c.1991G>C (p.Gly664Ala) | |
1 | g.16132236C>T | CA338622660 | EPHA2 | c.2153G>A (p.Gly718Asp) c.1991G>A (p.Gly664Asp) | dbSNP gnomAD v4 |
1 | g.16132237C>A | CA338622662 | EPHA2 | c.2152G>T (p.Gly718Cys) c.1990G>T (p.Gly664Cys) | |
1 | g.16132237C= | CA1155650216 | EPHA2 | c.2152G= (p.Gly718=) c.1990G= (p.Gly664=) | |
1 | g.16132237C>G | CA338622665 | EPHA2 | c.2152G>C (p.Gly718Arg) c.1990G>C (p.Gly664Arg) | |
1 | g.16132237C>T | CA338622668 | EPHA2 | c.2152G>A (p.Gly718Ser) c.1990G>A (p.Gly664Ser) | dbSNP |
1 | g.16132238C>A | CA416385695 | EPHA2 | c.2151G>T (p.Val717=) c.1989G>T (p.Val663=) | |
1 | g.16132238C>G | CA416385693 | EPHA2 | c.2151G>C (p.Val717=) c.1989G>C (p.Val663=) | dbSNP |
1 | g.16132238C>T | CA416385691 | EPHA2 | c.2151G>A (p.Val717=) c.1989G>A (p.Val663=) | |
1 | g.16132239A>C | CA338622671 | EPHA2 | c.2150T>G (p.Val717Gly) c.1988T>G (p.Val663Gly) | |
1 | g.16132239A>G | CA338622673 | EPHA2 | c.2150T>C (p.Val717Ala) c.1988T>C (p.Val663Ala) | |
1 | g.16132239A>T | CA338622676 | EPHA2 | c.2150T>A (p.Val717Glu) c.1988T>A (p.Val663Glu) | dbSNP |
1 | g.16132240C>A | CA338622681 | EPHA2 | c.2149G>T (p.Val717Leu) c.1987G>T (p.Val663Leu) | |
1 | g.16132240C= | CA1155650218 | EPHA2 | c.2149G= (p.Val717=) c.1987G= (p.Val663=) | |
1 | g.16132240C>G | CA338622682 | EPHA2 | c.2149G>C (p.Val717Leu) c.1987G>C (p.Val663Leu) | |
1 | g.16132240C>T | CA338622679 | EPHA2 | c.2149G>A (p.Val717Met) c.1987G>A (p.Val663Met) | dbSNP |
1 | g.16132241C>A | CA416385698 | EPHA2 | c.2148G>T (p.Leu716=) c.1986G>T (p.Leu662=) | gnomAD v4 |
1 | g.16132241C>G | CA416385699 | EPHA2 | c.2148G>C (p.Leu716=) c.1986G>C (p.Leu662=) |