Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
19 | g.48703566_48703567insGTGGCTCACGCCTATAATCTGAGCACTTTGGGAGGCCAAGGTGGG | CA9556296 | FUT2 | c.610_611insGTGGCTCACGCCTATAATCTGAGCACTTTGGGAGGCCAAGGTGGG (p.Asp204GlyfsTer6) n.285_286insACCTTGGCCTCCCAAAGTGCTCAGATTATAGGCGTGAGCCACCCC | dbSNP ExAC |
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 | |
19 | g.48703574C>A | CA508272201 | FUT2 | c.618C>A (p.Val206=) n.275G>T | |
19 | g.48703574C= | CA2340030129 | FUT2 | c.618C= (p.Val206=) n.275G= | |
19 | g.48703574C>G | CA508272202 | FUT2 | c.618C>G (p.Val206=) n.275G>C | gnomAD v4 |
19 | g.48703574C>T | CA508272203 | FUT2 | c.618C>T (p.Val206=) n.275G>A | dbSNP gnomAD v4 |
19 | g.48703575C>A | CA406711321 | FUT2 | c.619C>A (p.His207Asn) n.274G>T | |
19 | g.48703575C= | CA2340030130 | FUT2 | c.619C= (p.His207=) n.274G= | |
19 | g.48703575C>G | CA406711323 | FUT2 | c.619C>G (p.His207Asp) n.274G>C | |
19 | g.48703575C>T | CA9556297 | FUT2 | c.619C>T (p.His207Tyr) n.274G>A | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.48703576A= | CA2340030131 | FUT2 | c.620A= (p.His207=) n.273T= | |
19 | g.48703576A>C | CA406711326 | FUT2 | c.620A>C (p.His207Pro) n.273T>G | |
19 | g.48703576A>G | CA406711328 | FUT2 | c.620A>G (p.His207Arg) n.273T>C | dbSNP gnomAD v4 |
19 | g.48703576A>T | CA406711330 | FUT2 | c.620A>T (p.His207Leu) n.273T>A | |
19 | g.48703577T>A | CA406711331 | FUT2 | c.621T>A (p.His207Gln) n.272A>T | |
19 | g.48703577T>C | CA9556298 | FUT2 | c.621T>C (p.His207=) n.272A>G | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.48703577T>G | CA406711333 | FUT2 | c.621T>G (p.His207Gln) n.272A>C | dbSNP |
19 | g.48703577T= | CA2340030132 | FUT2 | c.621T= (p.His207=) n.272A= | |
19 | g.48703578G>A | CA406711335 | FUT2 | c.622G>A (p.Val208Ile) n.271C>T | |
19 | g.48703578G>C | CA9556299 | FUT2 | c.622G>C (p.Val208Leu) n.271C>G | dbSNP ExAC gnomAD v2 gnomAD v4 |
19 | g.48703578G= | CA2340030133 | FUT2 | c.622G= (p.Val208=) n.271C= | |
19 | g.48703578G>T | CA406711339 | FUT2 | c.622G>T (p.Val208Phe) n.271C>A | |
19 | g.48703579T>A | CA406711343 | FUT2 | c.623T>A (p.Val208Asp) n.270A>T | |
19 | g.48703579T>C | CA406711345 | FUT2 | c.623T>C (p.Val208Ala) n.270A>G |