| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 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 | |
| 19 | g.48703579T>G | CA406711347 | FUT2 | c.623T>G (p.Val208Gly) n.270A>C | |
| 19 | g.48703580C>A | CA508272204 | FUT2 | c.624C>A (p.Val208=) n.269G>T | |
| 19 | g.48703580C>G | CA508272205 | FUT2 | c.624C>G (p.Val208=) n.269G>C | |
| 19 | g.48703580C>T | CA508272206 | FUT2 | c.624C>T (p.Val208=) n.269G>A | gnomAD v4 |
| 19 | g.48703581A>C | CA406711354 | FUT2 | c.625A>C (p.Met209Leu) n.268T>G | |
| 19 | g.48703581A>G | CA406711350 | FUT2 | c.625A>G (p.Met209Val) n.268T>C | |
| 19 | g.48703581A>T | CA406711352 | FUT2 | c.625A>T (p.Met209Leu) n.268T>A | |
| 19 | g.48703582T>A | CA406711357 | FUT2 | c.626T>A (p.Met209Lys) n.267A>T | dbSNP gnomAD v3 gnomAD v4 |
| 19 | g.48703582T>C | CA406711359 | FUT2 | c.626T>C (p.Met209Thr) n.267A>G | gnomAD v4 |
| 19 | g.48703582T>G | CA406711361 | FUT2 | c.626T>G (p.Met209Arg) n.267A>C | |
| 19 | g.48703582T= | CA2340030134 | FUT2 | c.626T= (p.Met209=) n.267A= | |
| 19 | g.48703583G>A | CA406711364 | FUT2 | c.627G>A (p.Met209Ile) n.266C>T | dbSNP gnomAD v3 gnomAD v4 |
| 19 | g.48703583G>C | CA406711366 | FUT2 | c.627G>C (p.Met209Ile) n.266C>G | |
| 19 | g.48703583G= | CA2340030135 | FUT2 | c.627G= (p.Met209=) n.266C= | |
| 19 | g.48703583G>T | CA406711368 | FUT2 | c.627G>T (p.Met209Ile) n.266C>A | |
| 19 | g.48703584C>A | CA406711371 | FUT2 | c.628C>A (p.Pro210Thr) n.265G>T | |
| 19 | g.48703584C>G | CA406711374 | FUT2 | c.628C>G (p.Pro210Ala) n.265G>C | |
| 19 | g.48703584C>T | CA406711376 | FUT2 | c.628C>T (p.Pro210Ser) n.265G>A | |
| 19 | g.48703585C>A | CA406711379 | FUT2 | c.629C>A (p.Pro210Gln) n.264G>T | |
| 19 | g.48703585C>G | CA406711381 | FUT2 | c.629C>G (p.Pro210Arg) n.264G>C | |
| 19 | g.48703585C>T | CA406711383 | FUT2 | c.629C>T (p.Pro210Leu) n.264G>A | gnomAD v4 |
| 19 | g.48703586A= | CA2340030136 | FUT2 | c.630A= (p.Pro210=) n.263T= | |
| 19 | g.48703586A>C | CA9556300 | FUT2 | c.630A>C (p.Pro210=) n.263T>G | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 19 | g.48703586A>G | CA508272207 | FUT2 | c.630A>G (p.Pro210=) n.263T>C | gnomAD v4 |
| 19 | g.48703586A>T | CA508272208 | FUT2 | c.630A>T (p.Pro210=) n.263T>A |