Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
4 | g.73442357del | CA2531045514 | AFP | c.544del (p.Ala182LeufsTer7) c.541del (p.Ala181LeufsTer7) c.70del (p.Ala24LeufsTer7) | |
4 | g.73442356G>A | CA127856 | AFP | c.543G>A (p.Trp181Ter) c.540G>A (p.Trp180Ter) c.69G>A (p.Trp23Ter) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
4 | g.73442356G>C | CA357236642 | AFP | c.543G>C (p.Trp181Cys) c.540G>C (p.Trp180Cys) c.69G>C (p.Trp23Cys) | |
4 | g.73442356G= | CA1468178587 | AFP | c.543G= (p.Trp181=) c.540G= (p.Trp180=) c.69G= (p.Trp23=) | |
4 | g.73442356G>T | CA357236644 | AFP | c.543G>T (p.Trp181Cys) c.540G>T (p.Trp180Cys) c.69G>T (p.Trp23Cys) | |
4 | g.73442357G>A | CA2959946 | AFP | c.544G>A (p.Ala182Thr) c.541G>A (p.Ala181Thr) c.70G>A (p.Ala24Thr) | dbSNP ExAC gnomAD v2 gnomAD v4 |
4 | g.73442357G>C | CA357236648 | AFP | c.544G>C (p.Ala182Pro) c.541G>C (p.Ala181Pro) c.70G>C (p.Ala24Pro) | |
4 | g.73442357G= | CA1468178594 | AFP | c.544G= (p.Ala182=) c.541G= (p.Ala181=) c.70G= (p.Ala24=) | |
4 | g.73442357G>T | CA357236647 | AFP | c.544G>T (p.Ala182Ser) c.541G>T (p.Ala181Ser) c.70G>T (p.Ala24Ser) | |
4 | g.73442358C>A | CA357236650 | AFP | c.545C>A (p.Ala182Asp) c.542C>A (p.Ala181Asp) c.71C>A (p.Ala24Asp) | |
4 | g.73442358C= | CA1468178598 | AFP | c.545C= (p.Ala182=) c.542C= (p.Ala181=) c.71C= (p.Ala24=) | |
4 | g.73442358C>G | CA357236653 | AFP | c.545C>G (p.Ala182Gly) c.542C>G (p.Ala181Gly) c.71C>G (p.Ala24Gly) | COSMIC |
4 | g.73442358C>T | CA357236654 | AFP | c.545C>T (p.Ala182Val) c.542C>T (p.Ala181Val) c.71C>T (p.Ala24Val) | dbSNP gnomAD v2 COSMIC |
4 | g.73442359T>A | CA439800178 | AFP | c.546T>A (p.Ala182=) c.543T>A (p.Ala181=) c.72T>A (p.Ala24=) | |
4 | g.73442359T>C | CA439800179 | AFP | c.546T>C (p.Ala182=) c.543T>C (p.Ala181=) c.72T>C (p.Ala24=) | |
4 | g.73442359T>G | CA439800181 | AFP | c.546T>G (p.Ala182=) c.543T>G (p.Ala181=) c.72T>G (p.Ala24=) | |
4 | g.73442360G>A | CA357236657 | AFP | c.547G>A (p.Ala183Thr) c.544G>A (p.Ala182Thr) c.73G>A (p.Ala25Thr) | dbSNP |
4 | g.73442360G>C | CA357236659 | AFP | c.547G>C (p.Ala183Pro) c.544G>C (p.Ala182Pro) c.73G>C (p.Ala25Pro) | |
4 | g.73442360G= | CA1468178604 | AFP | c.547G= (p.Ala183=) c.544G= (p.Ala182=) c.73G= (p.Ala25=) | |
4 | g.73442360G>T | CA357236662 | AFP | c.547G>T (p.Ala183Ser) c.544G>T (p.Ala182Ser) c.73G>T (p.Ala25Ser) | |
4 | g.73442361C>A | CA357236664 | AFP | c.548C>A (p.Ala183Asp) c.545C>A (p.Ala182Asp) c.74C>A (p.Ala25Asp) | |
4 | g.73442361C= | CA1468178608 | AFP | c.548C= (p.Ala183=) c.545C= (p.Ala182=) c.74C= (p.Ala25=) | |
4 | g.73442361C>G | CA357236665 | AFP | c.548C>G (p.Ala183Gly) c.545C>G (p.Ala182Gly) c.74C>G (p.Ala25Gly) | |
4 | g.73442361C>T | CA2959947 | AFP | c.548C>T (p.Ala183Val) c.545C>T (p.Ala182Val) c.74C>T (p.Ala25Val) | dbSNP ExAC gnomAD v2 gnomAD v4 |
4 | g.73442362T>A | CA439800184 | AFP | c.549T>A (p.Ala183=) c.546T>A (p.Ala182=) c.75T>A (p.Ala25=) | |
4 | g.73442362T>C | CA439800186 | AFP | c.549T>C (p.Ala183=) c.546T>C (p.Ala182=) c.75T>C (p.Ala25=) | |
4 | g.73442362T>G | CA439800188 | AFP | c.549T>G (p.Ala183=) c.546T>G (p.Ala182=) c.75T>G (p.Ala25=) | |
4 | g.73442363C>A | CA357236666 | AFP | c.550C>A (p.Arg184Ser) c.547C>A (p.Arg183Ser) c.76C>A (p.Arg26Ser) | |
4 | g.73442363C= | CA1468178611 | AFP | c.550C= (p.Arg184=) c.547C= (p.Arg183=) c.76C= (p.Arg26=) | |
4 | g.73442363C>G | CA357236667 | AFP | c.550C>G (p.Arg184Gly) c.547C>G (p.Arg183Gly) c.76C>G (p.Arg26Gly) | gnomAD v4 |
4 | g.73442363C>T | CA2959948 | AFP | c.550C>T (p.Arg184Cys) c.547C>T (p.Arg183Cys) c.76C>T (p.Arg26Cys) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
4 | g.73442364G>A | CA357236669 | AFP | c.551G>A (p.Arg184His) c.548G>A (p.Arg183His) c.77G>A (p.Arg26His) | gnomAD v4 COSMIC |
4 | g.73442364G>C | CA357236670 | AFP | c.551G>C (p.Arg184Pro) c.548G>C (p.Arg183Pro) c.77G>C (p.Arg26Pro) | |
4 | g.73442364G>T | CA357236668 | AFP | c.551G>T (p.Arg184Leu) c.548G>T (p.Arg183Leu) c.77G>T (p.Arg26Leu) | gnomAD v4 |
4 | g.73442365C>A | CA99671617 | AFP | c.552C>A (p.Arg184=) c.549C>A (p.Arg183=) c.78C>A (p.Arg26=) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
4 | g.73442365C= | CA1468178614 | AFP | c.552C= (p.Arg184=) c.549C= (p.Arg183=) c.78C= (p.Arg26=) | |
4 | g.73442365C>G | CA439800191 | AFP | c.552C>G (p.Arg184=) c.549C>G (p.Arg183=) c.78C>G (p.Arg26=) | |
4 | g.73442365C>T | CA439800193 | AFP | c.552C>T (p.Arg184=) c.549C>T (p.Arg183=) c.78C>T (p.Arg26=) | dbSNP |
4 | g.73442366T>A | CA357236676 | AFP | c.553T>A (p.Tyr185Asn) c.550T>A (p.Tyr184Asn) c.79T>A (p.Tyr27Asn) | |
4 | g.73442366T>C | CA357236673 | AFP | c.553T>C (p.Tyr185His) c.550T>C (p.Tyr184His) c.79T>C (p.Tyr27His) | |
4 | g.73442366T>G | CA357236675 | AFP | c.553T>G (p.Tyr185Asp) c.550T>G (p.Tyr184Asp) c.79T>G (p.Tyr27Asp) | |
4 | g.73442367A= | CA1468178617 | AFP | c.554A= (p.Tyr185=) c.551A= (p.Tyr184=) c.80A= (p.Tyr27=) | |
4 | g.73442367A>C | CA357236679 | AFP | c.554A>C (p.Tyr185Ser) c.551A>C (p.Tyr184Ser) c.80A>C (p.Tyr27Ser) | gnomAD v4 |
4 | g.73442367A>G | CA357236681 | AFP | c.554A>G (p.Tyr185Cys) c.551A>G (p.Tyr184Cys) c.80A>G (p.Tyr27Cys) | dbSNP |
4 | g.73442367A>T | CA357236682 | AFP | c.554A>T (p.Tyr185Phe) c.551A>T (p.Tyr184Phe) c.80A>T (p.Tyr27Phe) | |
4 | g.73442368T>A | CA357236685 | AFP | c.555T>A (p.Tyr185Ter) c.552T>A (p.Tyr184Ter) c.81T>A (p.Tyr27Ter) | |
4 | g.73442368T>C | CA439800196 | AFP | c.555T>C (p.Tyr185=) c.552T>C (p.Tyr184=) c.81T>C (p.Tyr27=) | gnomAD v4 |
4 | g.73442368T>G | CA357236687 | AFP | c.555T>G (p.Tyr185Ter) c.552T>G (p.Tyr184Ter) c.81T>G (p.Tyr27Ter) | |
4 | g.73442369G>A | CA99671627 | AFP | c.556G>A (p.Asp186Asn) c.553G>A (p.Asp185Asn) c.82G>A (p.Asp28Asn) | dbSNP gnomAD v3 gnomAD v4 |
4 | g.73442369G>C | CA357236690 | AFP | c.556G>C (p.Asp186His) c.553G>C (p.Asp185His) c.82G>C (p.Asp28His) |