Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
19 | g.48703463C>A | CA508272595 | FUT2 | c.507C>A (p.Thr169=) n.386G>T | |
19 | g.48703463C>G | CA508272596 | FUT2 | c.507C>G (p.Thr169=) n.386G>C | |
19 | g.48703463C>T | CA508272597 | FUT2 | c.507C>T (p.Thr169=) n.386G>A | |
19 | g.48703464C>A | CA406710734 | FUT2 | c.508C>A (p.Leu170Met) n.385G>T | |
19 | g.48703464C= | CA2340030054 | FUT2 | c.508C= (p.Leu170=) n.385G= | |
19 | g.48703464C>G | CA406710736 | FUT2 | c.508C>G (p.Leu170Val) n.385G>C | |
19 | g.48703464C>T | CA508272598 | FUT2 | c.508C>T (p.Leu170=) n.385G>A | dbSNP gnomAD v4 |
19 | g.48703465T>A | CA406710739 | FUT2 | c.509T>A (p.Leu170Gln) n.384A>T | |
19 | g.48703465T>C | CA406710741 | FUT2 | c.509T>C (p.Leu170Pro) n.384A>G | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.48703465T>G | CA406710743 | FUT2 | c.509T>G (p.Leu170Arg) n.384A>C | |
19 | g.48703465T= | CA2340030055 | FUT2 | c.509T= (p.Leu170=) n.384A= | |
19 | g.48703466G>A | CA508272600 | FUT2 | c.510G>A (p.Leu170=) n.383C>T | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.48703466G>C | CA508272601 | FUT2 | c.510G>C (p.Leu170=) n.383C>G | |
19 | g.48703466G= | CA2340030056 | FUT2 | c.510G= (p.Leu170=) n.383C= | |
19 | g.48703466G>T | CA508272599 | FUT2 | c.510G>T (p.Leu170=) n.383C>A | |
19 | g.48703467C>A | CA406710748 | FUT2 | c.511C>A (p.His171Asn) n.382G>T | |
19 | g.48703467C= | CA2340030057 | FUT2 | c.511C= (p.His171=) n.382G= | |
19 | g.48703467C>G | CA406710751 | FUT2 | c.511C>G (p.His171Asp) n.382G>C | |
19 | g.48703467C>T | CA406710746 | FUT2 | c.511C>T (p.His171Tyr) n.382G>A | dbSNP gnomAD v2 gnomAD v4 |
19 | g.48703468A= | CA2340030058 | FUT2 | c.512A= (p.His171=) n.381T= | |
19 | g.48703468A>C | CA406710754 | FUT2 | c.512A>C (p.His171Pro) n.381T>G | |
19 | g.48703468A>G | CA406710756 | FUT2 | c.512A>G (p.His171Arg) n.381T>C | dbSNP |
19 | g.48703468A>T | CA406710758 | FUT2 | c.512A>T (p.His171Leu) n.381T>A | |
19 | g.48703469C>A | CA406710761 | FUT2 | c.513C>A (p.His171Gln) n.380G>T | |
19 | g.48703469C= | CA2340030059 | FUT2 | c.513C= (p.His171=) n.380G= | |
19 | g.48703469C>G | CA309352445 | FUT2 | c.513C>G (p.His171Gln) n.380G>C | dbSNP gnomAD v3 gnomAD v4 |
19 | g.48703469C>T | CA9556259 | FUT2 | c.513C>T (p.His171=) n.380G>A | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.48703470G>A | CA9556260 | FUT2 | c.514G>A (p.Asp172Asn) n.379C>T | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.48703470G>C | CA406710767 | FUT2 | c.514G>C (p.Asp172His) n.379C>G | |
19 | g.48703470G= | CA2340030060 | FUT2 | c.514G= (p.Asp172=) n.379C= | |
19 | g.48703470G>T | CA406710769 | FUT2 | c.514G>T (p.Asp172Tyr) n.379C>A | gnomAD v4 |
19 | g.48703471A= | CA2340030061 | FUT2 | c.515A= (p.Asp172=) n.378T= | |
19 | g.48703471A>C | CA406710773 | FUT2 | c.515A>C (p.Asp172Ala) n.378T>G | |
19 | g.48703471A>G | CA406710776 | FUT2 | c.515A>G (p.Asp172Gly) n.378T>C | dbSNP gnomAD v3 gnomAD v4 |
19 | g.48703471A>T | CA406710778 | FUT2 | c.515A>T (p.Asp172Val) n.378T>A | |
19 | g.48703472C>A | CA406710781 | FUT2 | c.516C>A (p.Asp172Glu) n.377G>T | |
19 | g.48703472C= | CA2340030062 | FUT2 | c.516C= (p.Asp172=) n.377G= | |
19 | g.48703472C>G | CA406710783 | FUT2 | c.516C>G (p.Asp172Glu) n.377G>C | dbSNP gnomAD v2 |
19 | g.48703472C>T | CA309352447 | FUT2 | c.516C>T (p.Asp172=) n.377G>A | dbSNP gnomAD v4 |
19 | g.48703473C>A | CA406710786 | FUT2 | c.517C>A (p.His173Asn) n.376G>T | |
19 | g.48703473C= | CA2340030063 | FUT2 | c.517C= (p.His173=) n.376G= | |
19 | g.48703473C>G | CA406710790 | FUT2 | c.517C>G (p.His173Asp) n.376G>C | dbSNP gnomAD v4 |
19 | g.48703473C>T | CA9556261 | FUT2 | c.517C>T (p.His173Tyr) n.376G>A | dbSNP ExAC gnomAD v2 gnomAD v4 |
19 | g.48703474A>C | CA406710792 | FUT2 | c.518A>C (p.His173Pro) n.375T>G | |
19 | g.48703474A>G | CA406710794 | FUT2 | c.518A>G (p.His173Arg) n.375T>C | |
19 | g.48703474A>T | CA406710795 | FUT2 | c.518A>T (p.His173Leu) n.375T>A | |
19 | g.48703475C>A | CA406710798 | FUT2 | c.519C>A (p.His173Gln) n.374G>T | |
19 | g.48703475C= | CA2340030064 | FUT2 | c.519C= (p.His173=) n.374G= | |
19 | g.48703475C>G | CA406710800 | FUT2 | c.519C>G (p.His173Gln) n.374G>C | |
19 | g.48703475C>T | CA9556262 | FUT2 | c.519C>T (p.His173=) n.374G>A | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |