Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
19 | g.48703281A>C | CA406709514 | FUT2 | c.325A>C (p.Ile109Leu) n.568T>G | |
19 | g.48703281A>G | CA406709518 | FUT2 | c.325A>G (p.Ile109Val) n.568T>C | |
19 | g.48703281A>T | CA406709521 | FUT2 | c.325A>T (p.Ile109Phe) n.568T>A | |
19 | g.48703282T>A | CA406709524 | FUT2 | c.326T>A (p.Ile109Asn) n.567A>T | gnomAD v4 |
19 | g.48703282T>C | CA406709527 | FUT2 | c.326T>C (p.Ile109Thr) n.567A>G | |
19 | g.48703282T>G | CA406709529 | FUT2 | c.326T>G (p.Ile109Ser) n.567A>C | |
19 | g.48703283C>A | CA508272246 | FUT2 | c.327C>A (p.Ile109=) n.566G>T | |
19 | g.48703283C>G | CA406709531 | FUT2 | c.327C>G (p.Ile109Met) n.566G>C | |
19 | g.48703283C>T | CA508272247 | FUT2 | c.327C>T (p.Ile109=) n.566G>A | |
19 | g.48703284A= | CA2340029948 | FUT2 | c.328A= (p.Thr110=) n.565T= | |
19 | g.48703284A>C | CA9556212 | FUT2 | c.328A>C (p.Thr110Pro) n.565T>G | dbSNP ExAC gnomAD v2 gnomAD v4 |
19 | g.48703284A>G | CA406709534 | FUT2 | c.328A>G (p.Thr110Ala) n.565T>C | gnomAD v4 |
19 | g.48703284A>T | CA406709536 | FUT2 | c.328A>T (p.Thr110Ser) n.565T>A | |
19 | g.48703285C>A | CA406709550 | FUT2 | c.329C>A (p.Thr110Asn) n.564G>T | |
19 | g.48703285C= | CA2340029949 | FUT2 | c.329C= (p.Thr110=) n.564G= | |
19 | g.48703285C>G | CA406709544 | FUT2 | c.329C>G (p.Thr110Ser) n.564G>C | |
19 | g.48703285C>T | CA9556213 | FUT2 | c.329C>T (p.Thr110Ile) n.564G>A | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.48703286C>A | CA508272249 | FUT2 | c.330C>A (p.Thr110=) n.563G>T | |
19 | g.48703286C= | CA2340029950 | FUT2 | c.330C= (p.Thr110=) n.563G= | |
19 | g.48703286C>G | CA508272250 | FUT2 | c.330C>G (p.Thr110=) n.563G>C | |
19 | g.48703286C>T | CA9556214 | FUT2 | c.330C>T (p.Thr110=) n.563G>A | dbSNP ExAC gnomAD v2 gnomAD v4 |
19 | g.48703287C>A | CA406709556 | FUT2 | c.331C>A (p.Leu111Met) n.562G>T | |
19 | g.48703287C>G | CA406709559 | FUT2 | c.331C>G (p.Leu111Val) n.562G>C | |
19 | g.48703287C>T | CA508272251 | FUT2 | c.331C>T (p.Leu111=) n.562G>A | |
19 | g.48703288T>A | CA406709562 | FUT2 | c.332T>A (p.Leu111Gln) n.561A>T | |
19 | g.48703288T>C | CA406709563 | FUT2 | c.332T>C (p.Leu111Pro) n.561A>G | dbSNP gnomAD v2 gnomAD v4 |
19 | g.48703288T>G | CA406709564 | FUT2 | c.332T>G (p.Leu111Arg) n.561A>C | |
19 | g.48703288T= | CA2340029951 | FUT2 | c.332T= (p.Leu111=) n.561A= | |
19 | g.48703289G>A | CA508272252 | FUT2 | c.333G>A (p.Leu111=) n.560C>T | dbSNP |
19 | g.48703289G>C | CA508272253 | FUT2 | c.333G>C (p.Leu111=) n.560C>G | |
19 | g.48703289G>T | CA508272254 | FUT2 | c.333G>T (p.Leu111=) n.560C>A | |
19 | g.48703290C>A | CA406709566 | FUT2 | c.334C>A (p.Pro112Thr) n.559G>T | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.48703290C= | CA2340029952 | FUT2 | c.334C= (p.Pro112=) n.559G= | |
19 | g.48703290C>G | CA406709568 | FUT2 | c.334C>G (p.Pro112Ala) n.559G>C | |
19 | g.48703290C>T | CA406709571 | FUT2 | c.334C>T (p.Pro112Ser) n.559G>A | |
19 | g.48703291C>A | CA406709576 | FUT2 | c.335C>A (p.Pro112Gln) n.558G>T | |
19 | g.48703291C= | CA2340029953 | FUT2 | c.335C= (p.Pro112=) n.558G= | |
19 | g.48703291C>G | CA406709580 | FUT2 | c.335C>G (p.Pro112Arg) n.558G>C | |
19 | g.48703291C>T | CA9556215 | FUT2 | c.335C>T (p.Pro112Leu) n.558G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.48703292G>A | CA9556216 | FUT2 | c.336G>A (p.Pro112=) n.557C>T | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.48703292G>C | CA508272257 | FUT2 | c.336G>C (p.Pro112=) n.557C>G | |
19 | g.48703292G= | CA2340029954 | FUT2 | c.336G= (p.Pro112=) n.557C= | |
19 | g.48703292G>T | CA508272258 | FUT2 | c.336G>T (p.Pro112=) n.557C>A | |
19 | g.48703293G>A | CA9556217 | FUT2 | c.337G>A (p.Val113Met) n.556C>T | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.48703293G>C | CA406709599 | FUT2 | c.337G>C (p.Val113Leu) n.556C>G | |
19 | g.48703293G= | CA2340029955 | FUT2 | c.337G= (p.Val113=) n.556C= | |
19 | g.48703293G>T | CA406709594 | FUT2 | c.337G>T (p.Val113Leu) n.556C>A | dbSNP |
19 | g.48703294T>A | CA406709610 | FUT2 | c.338T>A (p.Val113Glu) n.555A>T | |
19 | g.48703294T>C | CA406709617 | FUT2 | c.338T>C (p.Val113Ala) n.555A>G | |
19 | g.48703294T>G | CA406709612 | FUT2 | c.338T>G (p.Val113Gly) n.555A>C |