Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
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 | |
19 | g.48703173G>C | CA406709010 | FUT2 | c.217G>C (p.Gly73Arg) n.676C>G | gnomAD v4 |
19 | g.48703173G>T | CA406709012 | FUT2 | c.217G>T (p.Gly73Trp) n.676C>A | |
19 | g.48703174G>A | CA406709014 | FUT2 | c.218G>A (p.Gly73Glu) n.675C>T | |
19 | g.48703174G>C | CA406709016 | FUT2 | c.218G>C (p.Gly73Ala) n.675C>G | |
19 | g.48703174G>T | CA406709018 | FUT2 | c.218G>T (p.Gly73Val) n.675C>A | |
19 | g.48703175G>A | CA508272441 | FUT2 | c.219G>A (p.Gly73=) n.674C>T | dbSNP gnomAD v4 |
19 | g.48703175G>C | CA508272443 | FUT2 | c.219G>C (p.Gly73=) n.674C>G | |
19 | g.48703175G= | CA2340029891 | FUT2 | c.219G= (p.Gly73=) n.674C= | |
19 | g.48703175G>T | CA508272442 | FUT2 | c.219G>T (p.Gly73=) n.674C>A | |
19 | g.48703176A>C | CA406709024 | FUT2 | c.220A>C (p.Asn74His) n.673T>G | |
19 | g.48703176A>G | CA406709020 | FUT2 | c.220A>G (p.Asn74Asp) n.673T>C | |
19 | g.48703176A>T | CA406709022 | FUT2 | c.220A>T (p.Asn74Tyr) n.673T>A | |
19 | g.48703177A>C | CA406709026 | FUT2 | c.221A>C (p.Asn74Thr) n.672T>G | |
19 | g.48703177A>G | CA406709028 | FUT2 | c.221A>G (p.Asn74Ser) n.672T>C | |
19 | g.48703177A>T | CA406709029 | FUT2 | c.221A>T (p.Asn74Ile) n.672T>A | |
19 | g.48703178C>A | CA406709031 | FUT2 | c.222C>A (p.Asn74Lys) n.671G>T | |
19 | g.48703178C>G | CA406709032 | FUT2 | c.222C>G (p.Asn74Lys) n.671G>C | |
19 | g.48703178C>T | CA508272444 | FUT2 | c.222C>T (p.Asn74=) n.671G>A | dbSNP |
19 | g.48703179C>A | CA406709034 | FUT2 | c.223C>A (p.Gln75Lys) n.670G>T | |
19 | g.48703179C>G | CA406709038 | FUT2 | c.223C>G (p.Gln75Glu) n.670G>C | |
19 | g.48703179C>T | CA406709036 | FUT2 | c.223C>T (p.Gln75Ter) n.670G>A | |
19 | g.48703180A>C | CA406709040 | FUT2 | c.224A>C (p.Gln75Pro) n.669T>G | gnomAD v4 |
19 | g.48703180A>G | CA406709042 | FUT2 | c.224A>G (p.Gln75Arg) n.669T>C | gnomAD v4 |
19 | g.48703180A>T | CA406709044 | FUT2 | c.224A>T (p.Gln75Leu) n.669T>A | |
19 | g.48703181G>A | CA508272448 | FUT2 | c.225G>A (p.Gln75=) n.668C>T | |
19 | g.48703181G>C | CA406709046 | FUT2 | c.225G>C (p.Gln75His) n.668C>G | |
19 | g.48703181G= | CA2340029892 | FUT2 | c.225G= (p.Gln75=) n.668C= | |
19 | g.48703181G>T | CA406709048 | FUT2 | c.225G>T (p.Gln75His) n.668C>A | |
19 | g.48703182A>C | CA406709049 | FUT2 | c.226A>C (p.Met76Leu) n.667T>G | |
19 | g.48703182A>G | CA406709050 | FUT2 | c.226A>G (p.Met76Val) n.667T>C | |
19 | g.48703182A>T | CA406709052 | FUT2 | c.226A>T (p.Met76Leu) n.667T>A | |
19 | g.48703182dup | CA633888221 | FUT2 | c.226dup (p.Met76AsnfsTer?) n.667dup | dbSNP gnomAD v2 gnomAD v4 |
19 | g.48703183T>A | CA406709053 | FUT2 | c.227T>A (p.Met76Lys) n.666A>T | dbSNP gnomAD v2 gnomAD v4 |
19 | g.48703183T>C | CA406709055 | FUT2 | c.227T>C (p.Met76Thr) n.666A>G | |
19 | g.48703183T>G | CA406709057 | FUT2 | c.227T>G (p.Met76Arg) n.666A>C | gnomAD v4 |
19 | g.48703183T= | CA2340029893 | FUT2 | c.227T= (p.Met76=) n.666A= | |
19 | g.48703184G>A | CA406709062 | FUT2 | c.228G>A (p.Met76Ile) n.665C>T | |
19 | g.48703184G>C | CA406709063 | FUT2 | c.228G>C (p.Met76Ile) n.665C>G | |
19 | g.48703184G>T | CA406709059 | FUT2 | c.228G>T (p.Met76Ile) n.665C>A |