Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
19 | g.48702970A>C | CA406707942 | FUT2 | c.14A>C (p.Gln5Pro) n.879T>G | |
19 | g.48702970A>G | CA406707945 | FUT2 | c.14A>G (p.Gln5Arg) n.879T>C | |
19 | g.48702970A>T | CA406707946 | FUT2 | c.14A>T (p.Gln5Leu) n.879T>A | |
19 | g.48702971G>A | CA508271976 | FUT2 | c.15G>A (p.Gln5=) n.878C>T | |
19 | g.48702971G>C | CA406707954 | FUT2 | c.15G>C (p.Gln5His) n.878C>G | |
19 | g.48702971G>T | CA406707951 | FUT2 | c.15G>T (p.Gln5His) n.878C>A | |
19 | g.48702972A= | CA2340029785 | FUT2 | c.16A= (p.Met6=) n.877T= | |
19 | g.48702972A>C | CA406707959 | FUT2 | c.16A>C (p.Met6Leu) n.877T>G | |
19 | g.48702972A>G | CA9556120 | FUT2 | c.16A>G (p.Met6Val) n.877T>C | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.48702972A>T | CA406707961 | FUT2 | c.16A>T (p.Met6Leu) n.877T>A | |
19 | g.48702973T>A | CA406707966 | FUT2 | c.17T>A (p.Met6Lys) n.876A>T | |
19 | g.48702973T>C | CA406707970 | FUT2 | c.17T>C (p.Met6Thr) n.876A>G | |
19 | g.48702973T>G | CA406707969 | FUT2 | c.17T>G (p.Met6Arg) n.876A>C | |
19 | g.48702974G>A | CA406707975 | FUT2 | c.18G>A (p.Met6Ile) n.875C>T | dbSNP gnomAD v4 |
19 | g.48702974G>C | CA406707980 | FUT2 | c.18G>C (p.Met6Ile) n.875C>G | dbSNP gnomAD v4 |
19 | g.48702974G= | CA2340029786 | FUT2 | c.18G= (p.Met6=) n.875C= | |
19 | g.48702974G>T | CA406707978 | FUT2 | c.18G>T (p.Met6Ile) n.875C>A | |
19 | g.48702975C>A | CA9556121 | FUT2 | c.19C>A (p.Pro7Thr) n.874G>T | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.48702975C= | CA2340029787 | FUT2 | c.19C= (p.Pro7=) n.874G= | |
19 | g.48702975C>G | CA406707985 | FUT2 | c.19C>G (p.Pro7Ala) n.874G>C | gnomAD v4 |
19 | g.48702975C>T | CA406707987 | FUT2 | c.19C>T (p.Pro7Ser) n.874G>A | dbSNP gnomAD v2 gnomAD v4 |
19 | g.48702976C>A | CA406707992 | FUT2 | c.20C>A (p.Pro7His) n.873G>T | |
19 | g.48702976C>G | CA406707995 | FUT2 | c.20C>G (p.Pro7Arg) n.873G>C | |
19 | g.48702976C>T | CA406707998 | FUT2 | c.20C>T (p.Pro7Leu) n.873G>A | |
19 | g.48702977T>A | CA508271988 | FUT2 | c.21T>A (p.Pro7=) n.872A>T | |
19 | g.48702977T>C | CA9556122 | FUT2 | c.21T>C (p.Pro7=) n.872A>G | dbSNP ExAC gnomAD v2 gnomAD v4 |
19 | g.48702977T>G | CA508271990 | FUT2 | c.21T>G (p.Pro7=) n.872A>C | |
19 | g.48702977T= | CA2340029788 | FUT2 | c.21T= (p.Pro7=) n.872A= | |
19 | g.48702978T>A | CA406708003 | FUT2 | c.22T>A (p.Phe8Ile) n.871A>T | |
19 | g.48702978T>C | CA406708004 | FUT2 | c.22T>C (p.Phe8Leu) n.871A>G | |
19 | g.48702978T>G | CA406708005 | FUT2 | c.22T>G (p.Phe8Val) n.871A>C | |
19 | g.48702979T>A | CA406708007 | FUT2 | c.23T>A (p.Phe8Tyr) n.870A>T | |
19 | g.48702979T>C | CA406708013 | FUT2 | c.23T>C (p.Phe8Ser) n.870A>G | gnomAD v4 |
19 | g.48702979T>G | CA406708015 | FUT2 | c.23T>G (p.Phe8Cys) n.870A>C | |
19 | g.48702980C>A | CA406708020 | FUT2 | c.24C>A (p.Phe8Leu) n.869G>T | |
19 | g.48702980C>G | CA406708023 | FUT2 | c.24C>G (p.Phe8Leu) n.869G>C | |
19 | g.48702980C>T | CA508271996 | FUT2 | c.24C>T (p.Phe8=) n.869G>A | gnomAD v4 |
19 | g.48702981T>A | CA406708027 | FUT2 | c.25T>A (p.Ser9Thr) n.868A>T | |
19 | g.48702981T>C | CA406708031 | FUT2 | c.25T>C (p.Ser9Pro) n.868A>G | |
19 | g.48702981T>G | CA406708034 | FUT2 | c.25T>G (p.Ser9Ala) n.868A>C | |
19 | g.48702982C>A | CA406708038 | FUT2 | c.26C>A (p.Ser9Tyr) n.867G>T | gnomAD v4 |
19 | g.48702982C= | CA2340029789 | FUT2 | c.26C= (p.Ser9=) n.867G= | |
19 | g.48702982C>G | CA406708039 | FUT2 | c.26C>G (p.Ser9Cys) n.867G>C | dbSNP |
19 | g.48702982C>T | CA406708047 | FUT2 | c.26C>T (p.Ser9Phe) n.867G>A | |
19 | g.48702983C>A | CA508272000 | FUT2 | c.27C>A (p.Ser9=) n.866G>T | |
19 | g.48702983C>G | CA508272001 | FUT2 | c.27C>G (p.Ser9=) n.866G>C | |
19 | g.48702983C>T | CA508272002 | FUT2 | c.27C>T (p.Ser9=) n.866G>A | |
19 | g.48702984T>A | CA406708049 | FUT2 | c.28T>A (p.Phe10Ile) n.865A>T | |
19 | g.48702984T>C | CA406708052 | FUT2 | c.28T>C (p.Phe10Leu) n.865A>G | |
19 | g.48702984T>G | CA406708055 | FUT2 | c.28T>G (p.Phe10Val) n.865A>C |