Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
19 | g.48703073G>A | CA406708594 | FUT2 | c.117G>A (p.Trp39Ter) n.776C>T | dbSNP |
19 | g.48703073G>C | CA406708596 | FUT2 | c.117G>C (p.Trp39Cys) n.776C>G | |
19 | g.48703073G= | CA2340029834 | FUT2 | c.117G= (p.Trp39=) n.776C= | |
19 | g.48703073G>T | CA406708597 | FUT2 | c.117G>T (p.Trp39Cys) n.776C>A | |
19 | g.48703074G>A | CA406708599 | FUT2 | c.118G>A (p.Glu40Lys) n.775C>T | dbSNP gnomAD v3 gnomAD v4 |
19 | g.48703074G>C | CA406708600 | FUT2 | c.118G>C (p.Glu40Gln) n.775C>G | |
19 | g.48703074G>T | CA406708601 | FUT2 | c.118G>T (p.Glu40Ter) n.775C>A | |
19 | g.48703075A>C | CA406708606 | FUT2 | c.119A>C (p.Glu40Ala) n.774T>G | |
19 | g.48703075A>G | CA406708604 | FUT2 | c.119A>G (p.Glu40Gly) n.774T>C | |
19 | g.48703075A>T | CA406708603 | FUT2 | c.119A>T (p.Glu40Val) n.774T>A | |
19 | g.48703076G>A | CA508272330 | FUT2 | c.120G>A (p.Glu40=) n.773C>T | |
19 | g.48703076G>C | CA406708607 | FUT2 | c.120G>C (p.Glu40Asp) n.773C>G | |
19 | g.48703076G>T | CA406708609 | FUT2 | c.120G>T (p.Glu40Asp) n.773C>A | |
19 | g.48703077T>A | CA406708612 | FUT2 | c.121T>A (p.Leu41Ile) n.772A>T | |
19 | g.48703077T>C | CA508272331 | FUT2 | c.121T>C (p.Leu41=) n.772A>G | |
19 | g.48703077T>G | CA406708613 | FUT2 | c.121T>G (p.Leu41Val) n.772A>C | |
19 | g.48703078T>A | CA406708616 | FUT2 | c.122T>A (p.Leu41Ter) n.771A>T | |
19 | g.48703078T>C | CA406708620 | FUT2 | c.122T>C (p.Leu41Ser) n.771A>G | |
19 | g.48703078T>G | CA406708618 | FUT2 | c.122T>G (p.Leu41Ter) n.771A>C | |
19 | g.48703079A>C | CA406708622 | FUT2 | c.123A>C (p.Leu41Phe) n.770T>G | |
19 | g.48703079A>G | CA508272333 | FUT2 | c.123A>G (p.Leu41=) n.770T>C | |
19 | g.48703079A>T | CA406708623 | FUT2 | c.123A>T (p.Leu41Phe) n.770T>A | |
19 | g.48703080C>A | CA406708626 | FUT2 | c.124C>A (p.Pro42Thr) n.769G>T | dbSNP gnomAD v4 |
19 | g.48703080C= | CA2340029835 | FUT2 | c.124C= (p.Pro42=) n.769G= | |
19 | g.48703080C>G | CA406708627 | FUT2 | c.124C>G (p.Pro42Ala) n.769G>C | |
19 | g.48703080C>T | CA406708629 | FUT2 | c.124C>T (p.Pro42Ser) n.769G>A | |
19 | g.48703081C>A | CA406708631 | FUT2 | c.125C>A (p.Pro42Gln) n.768G>T | |
19 | g.48703081C= | CA2340029836 | FUT2 | c.125C= (p.Pro42=) n.768G= | |
19 | g.48703081C>G | CA406708633 | FUT2 | c.125C>G (p.Pro42Arg) n.768G>C | |
19 | g.48703081C>T | CA9556153 | FUT2 | c.125C>T (p.Pro42Leu) n.768G>A | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.48703081_48703082insCA | CA2340029837 | FUT2 | c.125_126insCA (p.Val43ArgfsTer7) n.767_768insTG | dbSNP |
19 | g.48703082G>A | CA9556154 | FUT2 | c.126G>A (p.Pro42=) n.767C>T | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.48703082G>C | CA508272334 | FUT2 | c.126G>C (p.Pro42=) n.767C>G | dbSNP |
19 | g.48703082G= | CA2340029838 | FUT2 | c.126G= (p.Pro42=) n.767C= | |
19 | g.48703082G>T | CA508272335 | FUT2 | c.126G>T (p.Pro42=) n.767C>A | gnomAD v4 |
19 | g.48703082_48703083del | CA2586240150 | FUT2 | c.126_127del (p.Val43AlafsTer?) n.766_767del | gnomAD v4 |
19 | g.48703083G>A | CA406708637 | FUT2 | c.127G>A (p.Val43Met) n.766C>T | dbSNP gnomAD v4 |
19 | g.48703083G>C | CA406708639 | FUT2 | c.127G>C (p.Val43Leu) n.766C>G | |
19 | g.48703083G= | CA2340029839 | FUT2 | c.127G= (p.Val43=) n.766C= | |
19 | g.48703083G>T | CA406708641 | FUT2 | c.127G>T (p.Val43Leu) n.766C>A | |
19 | g.48703084T>A | CA406708645 | FUT2 | c.128T>A (p.Val43Glu) n.765A>T | |
19 | g.48703084T>C | CA406708643 | FUT2 | c.128T>C (p.Val43Ala) n.765A>G | |
19 | g.48703084T>G | CA406708644 | FUT2 | c.128T>G (p.Val43Gly) n.765A>C | |
19 | g.48703085G>A | CA9556155 | FUT2 | c.129G>A (p.Val43=) n.764C>T | dbSNP ExAC gnomAD v2 gnomAD v4 |
19 | g.48703085G>C | CA508272337 | FUT2 | c.129G>C (p.Val43=) n.764C>G | |
19 | g.48703085G= | CA2340029840 | FUT2 | c.129G= (p.Val43=) n.764C= | |
19 | g.48703085G>T | CA508272336 | FUT2 | c.129G>T (p.Val43=) n.764C>A | |
19 | g.48703086C>A | CA406708648 | FUT2 | c.130C>A (p.Gln44Lys) n.763G>T | |
19 | g.48703086C= | CA2340029841 | FUT2 | c.130C= (p.Gln44=) n.763G= | |
19 | g.48703086C>G | CA406708650 | FUT2 | c.130C>G (p.Gln44Glu) n.763G>C |