Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
19 | g.48703064A>C | CA406708554 | FUT2 | c.108A>C (p.Gln36His) n.785T>G | |
19 | g.48703064A>G | CA508272326 | FUT2 | c.108A>G (p.Gln36=) n.785T>C | |
19 | g.48703064A>T | CA406708555 | FUT2 | c.108A>T (p.Gln36His) n.785T>A | |
19 | g.48703065G>A | CA9556151 | FUT2 | c.109G>A (p.Ala37Thr) n.784C>T | dbSNP ExAC gnomAD v2 gnomAD v4 |
19 | g.48703065G>C | CA406708558 | FUT2 | c.109G>C (p.Ala37Pro) n.784C>G | |
19 | g.48703065G= | CA2340029831 | FUT2 | c.109G= (p.Ala37=) n.784C= | |
19 | g.48703065G>T | CA406708559 | FUT2 | c.109G>T (p.Ala37Ser) n.784C>A | |
19 | g.48703066C>A | CA406708565 | FUT2 | c.110C>A (p.Ala37Asp) n.783G>T | |
19 | g.48703066C>G | CA406708564 | FUT2 | c.110C>G (p.Ala37Gly) n.783G>C | |
19 | g.48703066C>T | CA406708562 | FUT2 | c.110C>T (p.Ala37Val) n.783G>A | |
19 | g.48703067C>A | CA508272327 | FUT2 | c.111C>A (p.Ala37=) n.782G>T | |
19 | g.48703067C= | CA2340029832 | FUT2 | c.111C= (p.Ala37=) n.782G= | |
19 | g.48703067C>G | CA508272328 | FUT2 | c.111C>G (p.Ala37=) n.782G>C | |
19 | g.48703067C>T | CA508272329 | FUT2 | c.111C>T (p.Ala37=) n.782G>A | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.48703068A>C | CA406708568 | FUT2 | c.112A>C (p.Met38Leu) n.781T>G | |
19 | g.48703068A>G | CA406708569 | FUT2 | c.112A>G (p.Met38Val) n.781T>C | |
19 | g.48703068A>T | CA406708571 | FUT2 | c.112A>T (p.Met38Leu) n.781T>A | gnomAD v4 |
19 | g.48703069T>A | CA406708573 | FUT2 | c.113T>A (p.Met38Lys) n.780A>T | |
19 | g.48703069T>C | CA9556152 | FUT2 | c.113T>C (p.Met38Thr) n.780A>G | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.48703069T>G | CA406708575 | FUT2 | c.113T>G (p.Met38Arg) n.780A>C | |
19 | g.48703069T= | CA2340029833 | FUT2 | c.113T= (p.Met38=) n.780A= | |
19 | g.48703070G>A | CA406708578 | FUT2 | c.114G>A (p.Met38Ile) n.779C>T | |
19 | g.48703070G>C | CA406708581 | FUT2 | c.114G>C (p.Met38Ile) n.779C>G | |
19 | g.48703070G>T | CA406708580 | FUT2 | c.114G>T (p.Met38Ile) n.779C>A | |
19 | g.48703071T>A | CA406708583 | FUT2 | c.115T>A (p.Trp39Arg) n.778A>T | |
19 | g.48703071T>C | CA406708585 | FUT2 | c.115T>C (p.Trp39Arg) n.778A>G | |
19 | g.48703071T>G | CA406708587 | FUT2 | c.115T>G (p.Trp39Gly) n.778A>C | |
19 | g.48703072G>A | CA406708588 | FUT2 | c.116G>A (p.Trp39Ter) n.777C>T | |
19 | g.48703072G>C | CA406708590 | FUT2 | c.116G>C (p.Trp39Ser) n.777C>G | |
19 | g.48703072G>T | CA406708592 | FUT2 | c.116G>T (p.Trp39Leu) n.777C>A | |
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 |