Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
19 | g.48703157_48703167delinsTGCAATAGGCC | CA2340029879 | FUT2 | c.201_211delinsTGCAATAGGCC (p.Asn67=) n.682_692delinsGGCCTATTGCA | |
19 | g.48703160_48703169del | CA9556172 | FUT2 | c.204_213del (p.Ile69TrpfsTer17) n.682_691del | dbSNP ExAC gnomAD v2 gnomAD v4 |
19 | g.48703160A= | CA2340029883 | FUT2 | c.204A= (p.Ala68=) n.689T= | |
19 | g.48703160A>C | CA508272423 | FUT2 | c.204A>C (p.Ala68=) n.689T>G | gnomAD v4 |
19 | g.48703160A>G | CA9556174 | FUT2 | c.204A>G (p.Ala68=) n.689T>C | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.48703160A>T | CA508272424 | FUT2 | c.204A>T (p.Ala68=) n.689T>A | dbSNP |
19 | g.48703161A= | CA2340029884 | FUT2 | c.205A= (p.Ile69=) n.688T= | |
19 | g.48703161A>C | CA406708966 | FUT2 | c.205A>C (p.Ile69Leu) n.688T>G | |
19 | g.48703161A>G | CA406708969 | FUT2 | c.205A>G (p.Ile69Val) n.688T>C | dbSNP gnomAD v4 |
19 | g.48703161A>T | CA406708968 | FUT2 | c.205A>T (p.Ile69Leu) n.688T>A | |
19 | g.48703162T>A | CA406708971 | FUT2 | c.206T>A (p.Ile69Lys) n.687A>T | |
19 | g.48703162T>C | CA406708973 | FUT2 | c.206T>C (p.Ile69Thr) n.687A>G | dbSNP gnomAD v2 gnomAD v4 |
19 | g.48703162T>G | CA406708974 | FUT2 | c.206T>G (p.Ile69Arg) n.687A>C | |
19 | g.48703162T= | CA2340029885 | FUT2 | c.206T= (p.Ile69=) n.687A= | |
19 | g.48703163A>C | CA508272426 | FUT2 | c.207A>C (p.Ile69=) n.686T>G | |
19 | g.48703163A>G | CA406708976 | FUT2 | c.207A>G (p.Ile69Met) n.686T>C | |
19 | g.48703163A>T | CA508272427 | FUT2 | c.207A>T (p.Ile69=) n.686T>A | |
19 | g.48703164G>A | CA406708978 | FUT2 | c.208G>A (p.Gly70Ser) n.685C>T | dbSNP gnomAD v2 gnomAD v4 |
19 | g.48703164G>C | CA406708980 | FUT2 | c.208G>C (p.Gly70Arg) n.685C>G | |
19 | g.48703164G= | CA2340029886 | FUT2 | c.208G= (p.Gly70=) n.685C= | |
19 | g.48703164G>T | CA406708979 | FUT2 | c.208G>T (p.Gly70Cys) n.685C>A | |
19 | g.48703165G>A | CA406708983 | FUT2 | c.209G>A (p.Gly70Asp) n.684C>T | gnomAD v4 |
19 | g.48703165G>C | CA406708985 | FUT2 | c.209G>C (p.Gly70Ala) n.684C>G | |
19 | g.48703165G>T | CA406708986 | FUT2 | c.209G>T (p.Gly70Val) n.684C>A | |
19 | g.48703166C>A | CA508272429 | FUT2 | c.210C>A (p.Gly70=) n.683G>T | gnomAD v4 |
19 | g.48703166C>G | CA508272430 | FUT2 | c.210C>G (p.Gly70=) n.683G>C | |
19 | g.48703166C>T | CA508272431 | FUT2 | c.210C>T (p.Gly70=) n.683G>A | |
19 | g.48703167C>A | CA406708989 | FUT2 | c.211C>A (p.Arg71Ser) n.682G>T | |
19 | g.48703167C= | CA2340029887 | FUT2 | c.211C= (p.Arg71=) n.682G= | |
19 | g.48703167C>G | CA406708991 | FUT2 | c.211C>G (p.Arg71Gly) n.682G>C | |
19 | g.48703167C>T | CA9556175 | FUT2 | c.211C>T (p.Arg71Cys) n.682G>A | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.48703168G>A | CA9556176 | FUT2 | c.212G>A (p.Arg71His) n.681C>T | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
19 | g.48703168G>C | CA406708994 | FUT2 | c.212G>C (p.Arg71Pro) n.681C>G | |
19 | g.48703168G= | CA2340029888 | FUT2 | c.212G= (p.Arg71=) n.681C= | |
19 | g.48703168G>T | CA406708996 | FUT2 | c.212G>T (p.Arg71Leu) n.681C>A | gnomAD v4 |
19 | g.48703169C>A | CA508272432 | FUT2 | c.213C>A (p.Arg71=) n.680G>T | |
19 | g.48703169C= | CA2340029889 | FUT2 | c.213C= (p.Arg71=) n.680G= | |
19 | g.48703169C>G | CA508272433 | FUT2 | c.213C>G (p.Arg71=) n.680G>C | |
19 | g.48703169C>T | CA9556177 | FUT2 | c.213C>T (p.Arg71=) n.680G>A | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.48703170C>A | CA406708999 | FUT2 | c.214C>A (p.Leu72Met) n.679G>T | |
19 | g.48703170C= | CA2340029890 | FUT2 | c.214C= (p.Leu72=) n.679G= | |
19 | g.48703170C>G | CA406709001 | FUT2 | c.214C>G (p.Leu72Val) n.679G>C | |
19 | g.48703170C>T | CA508272436 | FUT2 | c.214C>T (p.Leu72=) n.679G>A | dbSNP gnomAD v2 gnomAD v4 |
19 | g.48703171T>A | CA406709003 | FUT2 | c.215T>A (p.Leu72Gln) n.678A>T | |
19 | g.48703171T>C | CA406709007 | FUT2 | c.215T>C (p.Leu72Pro) n.678A>G | |
19 | g.48703171T>G | CA406709005 | FUT2 | c.215T>G (p.Leu72Arg) n.678A>C | |
19 | g.48703172G>A | CA508272440 | FUT2 | c.216G>A (p.Leu72=) n.677C>T | |
19 | g.48703172G>C | CA508272439 | FUT2 | c.216G>C (p.Leu72=) n.677C>G | |
19 | g.48703172G>T | CA508272438 | FUT2 | c.216G>T (p.Leu72=) n.677C>A | |
19 | g.48703173G>A | CA406709008 | FUT2 | c.217G>A (p.Gly73Arg) n.676C>T |