Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
19 | g.48703560C>A | CA508272194 | FUT2 | c.604C>A (p.Arg202=) n.289G>T | |
19 | g.48703560C= | CA2340030122 | FUT2 | c.604C= (p.Arg202=) n.289G= | |
19 | g.48703560C>G | CA406711244 | FUT2 | c.604C>G (p.Arg202Gly) n.289G>C | dbSNP gnomAD v3 gnomAD v4 |
19 | g.48703560C>T | CA9556294 | FUT2 | c.604C>T (p.Arg202Ter) n.289G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.48703561G>A | CA9556295 | FUT2 | c.605G>A (p.Arg202Gln) n.288C>T | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.48703561G>C | CA406711251 | FUT2 | c.605G>C (p.Arg202Pro) n.288C>G | |
19 | g.48703561G= | CA2340030123 | FUT2 | c.605G= (p.Arg202=) n.288C= | |
19 | g.48703561G>T | CA406711250 | FUT2 | c.605G>T (p.Arg202Leu) n.288C>A | gnomAD v4 |
19 | g.48703562A>C | CA508272195 | FUT2 | c.606A>C (p.Arg202=) n.287T>G | |
19 | g.48703562A>G | CA508272196 | FUT2 | c.606A>G (p.Arg202=) n.287T>C | |
19 | g.48703562A>T | CA508272197 | FUT2 | c.606A>T (p.Arg202=) n.287T>A | |
19 | g.48703563G>A | CA406711254 | FUT2 | c.607G>A (p.Gly203Arg) n.286C>T | dbSNP gnomAD v3 gnomAD v4 |
19 | g.48703563G>C | CA406711259 | FUT2 | c.607G>C (p.Gly203Arg) n.286C>G | |
19 | g.48703563G= | CA2340030124 | FUT2 | c.607G= (p.Gly203=) n.286C= | |
19 | g.48703563G>T | CA406711256 | FUT2 | c.607G>T (p.Gly203Trp) n.286C>A | |
19 | g.48703564G>A | CA406711265 | FUT2 | c.608G>A (p.Gly203Glu) n.285C>T | |
19 | g.48703564G>C | CA406711267 | FUT2 | c.608G>C (p.Gly203Ala) n.285C>G | |
19 | g.48703564G>T | CA406711263 | FUT2 | c.608G>T (p.Gly203Val) n.285C>A | |
19 | g.48703566_48703567insGTGGCTCACGCCTATAATCTGAGCACTTTGGGAGGCCAAGGTGGG | CA9556296 | FUT2 | c.610_611insGTGGCTCACGCCTATAATCTGAGCACTTTGGGAGGCCAAGGTGGG (p.Asp204GlyfsTer6) n.285_286insACCTTGGCCTCCCAAAGTGCTCAGATTATAGGCGTGAGCCACCCC | dbSNP ExAC |
19 | g.48703565G>A | CA309352492 | FUT2 | c.609G>A (p.Gly203=) n.284C>T | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.48703565G>C | CA508272198 | FUT2 | c.609G>C (p.Gly203=) n.284C>G | |
19 | g.48703565G= | CA2340030125 | FUT2 | c.609G= (p.Gly203=) n.284C= | |
19 | g.48703565G>T | CA508272199 | FUT2 | c.609G>T (p.Gly203=) n.284C>A | dbSNP gnomAD v4 |
19 | g.48703566G>A | CA406711269 | FUT2 | c.610G>A (p.Asp204Asn) n.283C>T | |
19 | g.48703566G>C | CA406711272 | FUT2 | c.610G>C (p.Asp204His) n.283C>G | |
19 | g.48703566G>T | CA406711273 | FUT2 | c.610G>T (p.Asp204Tyr) n.283C>A | gnomAD v4 |
19 | g.48703567A= | CA2340030126 | FUT2 | c.611A= (p.Asp204=) n.282T= | |
19 | g.48703567A>C | CA406711277 | FUT2 | c.611A>C (p.Asp204Ala) n.282T>G | |
19 | g.48703567A>G | CA406711281 | FUT2 | c.611A>G (p.Asp204Gly) n.282T>C | |
19 | g.48703567A>T | CA406711283 | FUT2 | c.611A>T (p.Asp204Val) n.282T>A | dbSNP gnomAD v2 |
19 | g.48703568C>A | CA406711286 | FUT2 | c.612C>A (p.Asp204Glu) n.281G>T | |
19 | g.48703568C= | CA2340030127 | FUT2 | c.612C= (p.Asp204=) n.281G= | |
19 | g.48703568C>G | CA406711288 | FUT2 | c.612C>G (p.Asp204Glu) n.281G>C | gnomAD v4 |
19 | g.48703568C>T | CA309352494 | FUT2 | c.612C>T (p.Asp204=) n.281G>A | dbSNP |
19 | g.48703569T>A | CA406711296 | FUT2 | c.613T>A (p.Tyr205Asn) n.280A>T | |
19 | g.48703569T>C | CA406711294 | FUT2 | c.613T>C (p.Tyr205His) n.280A>G | gnomAD v4 |
19 | g.48703569T>G | CA406711292 | FUT2 | c.613T>G (p.Tyr205Asp) n.280A>C | |
19 | g.48703570A>C | CA406711299 | FUT2 | c.614A>C (p.Tyr205Ser) n.279T>G | |
19 | g.48703570A>G | CA406711300 | FUT2 | c.614A>G (p.Tyr205Cys) n.279T>C | gnomAD v4 |
19 | g.48703570A>T | CA406711303 | FUT2 | c.614A>T (p.Tyr205Phe) n.279T>A | |
19 | g.48703571T>A | CA406711305 | FUT2 | c.615T>A (p.Tyr205Ter) n.278A>T | gnomAD v4 |
19 | g.48703571T>C | CA508272200 | FUT2 | c.615T>C (p.Tyr205=) n.278A>G | dbSNP gnomAD v3 gnomAD v4 |
19 | g.48703571T>G | CA406711306 | FUT2 | c.615T>G (p.Tyr205Ter) n.278A>C | |
19 | g.48703571T= | CA2340030128 | FUT2 | c.615T= (p.Tyr205=) n.278A= | |
19 | g.48703572G>A | CA406711309 | FUT2 | c.616G>A (p.Val206Ile) n.277C>T | |
19 | g.48703572G>C | CA406711311 | FUT2 | c.616G>C (p.Val206Leu) n.277C>G | |
19 | g.48703572G>T | CA406711313 | FUT2 | c.616G>T (p.Val206Phe) n.277C>A | |
19 | g.48703573T>A | CA406711314 | FUT2 | c.617T>A (p.Val206Asp) n.276A>T | |
19 | g.48703573T>C | CA406711315 | FUT2 | c.617T>C (p.Val206Ala) n.276A>G | |
19 | g.48703573T>G | CA406711316 | FUT2 | c.617T>G (p.Val206Gly) n.276A>C |