Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
6 | g.49457753A= | CA1627392091 | MMUT | c.691T= (p.Tyr231=) | |
6 | g.49457753A>C | CA364404070 | MMUT | c.691T>G (p.Tyr231Asp) | |
6 | g.49457753A>G | CA364404073 | MMUT | c.691T>C (p.Tyr231His) | |
6 | g.49457753A>T | CA347881 | MMUT | c.691T>A (p.Tyr231Asn) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
6 | g.49457754T>A | CA450608767 | MMUT | c.690A>T (p.Thr230=) | dbSNP |
6 | g.49457754T>C | CA450608768 | MMUT | c.690A>G (p.Thr230=) | ClinVar gnomAD v4 COSMIC |
6 | g.49457754T>G | CA450608769 | MMUT | c.690A>C (p.Thr230=) | |
6 | g.49457754T= | CA1627392092 | MMUT | c.690A= (p.Thr230=) | |
6 | g.49457755_49457756del | CA2499218332 | MMUT | c.689_690del (p.Thr230IlefsTer14) | ClinVar dbSNP |
6 | g.49457755G>A | CA364404076 | MMUT | c.689C>T (p.Thr230Ile) | ClinVar dbSNP |
6 | g.49457755G>C | CA10575878 | MMUT | c.689C>G (p.Thr230Arg) | ClinVar dbSNP gnomAD v4 |
6 | g.49457755G= | CA1627392093 | MMUT | c.689C= (p.Thr230=) | |
6 | g.49457755G>T | CA364404077 | MMUT | c.689C>A (p.Thr230Lys) | COSMIC |
6 | g.49457756T>A | CA364404079 | MMUT | c.688A>T (p.Thr230Ser) | |
6 | g.49457756T>C | CA364404082 | MMUT | c.688A>G (p.Thr230Ala) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
6 | g.49457756T>G | CA364404085 | MMUT | c.688A>C (p.Thr230Pro) | |
6 | g.49457756T= | CA1627392094 | MMUT | c.688A= (p.Thr230=) | |
6 | g.49457757A= | CA1627392095 | MMUT | c.687T= (p.Asn229=) | |
6 | g.49457757A>C | CA364404089 | MMUT | c.687T>G (p.Asn229Lys) | |
6 | g.49457757A>G | CA3847069 | MMUT | c.687T>C (p.Asn229=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
6 | g.49457757A>T | CA364404104 | MMUT | c.687T>A (p.Asn229Lys) | gnomAD v4 |
6 | g.49457758T>A | CA364404107 | MMUT | c.686A>T (p.Asn229Ile) | |
6 | g.49457758T>C | CA364404110 | MMUT | c.686A>G (p.Asn229Ser) | |
6 | g.49457758T>G | CA364404113 | MMUT | c.686A>C (p.Asn229Thr) | |
6 | g.49457759T>A | CA364404116 | MMUT | c.685A>T (p.Asn229Tyr) | |
6 | g.49457759T>C | CA364404114 | MMUT | c.685A>G (p.Asn229Asp) | |
6 | g.49457759T>G | CA364404115 | MMUT | c.685A>C (p.Asn229His) | |
6 | g.49457760T>A | CA450608770 | MMUT | c.684A>T (p.Arg228=) | |
6 | g.49457760T>C | CA450608771 | MMUT | c.684A>G (p.Arg228=) | |
6 | g.49457760T>G | CA450608772 | MMUT | c.684A>C (p.Arg228=) | |
6 | g.49457761C>A | CA3847071 | MMUT | c.683G>T (p.Arg228Leu) | dbSNP ExAC gnomAD v2 |
6 | g.49457761C= | CA1627392096 | MMUT | c.683G= (p.Arg228=) | |
6 | g.49457761C>G | CA364404118 | MMUT | c.683G>C (p.Arg228Pro) | |
6 | g.49457761C>T | CA3847070 | MMUT | c.683G>A (p.Arg228Gln) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
6 | g.49457762G>A | CA312778 | MMUT | c.682C>T (p.Arg228Ter) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
6 | g.49457762G>C | CA364404123 | MMUT | c.682C>G (p.Arg228Gly) | |
6 | g.49457762G= | CA1627392097 | MMUT | c.682C= (p.Arg228=) | |
6 | g.49457762G>T | CA450608773 | MMUT | c.682C>A (p.Arg228=) | |
6 | g.49457763A= | CA1627392098 | MMUT | c.681T= (p.Val227=) | |
6 | g.49457763A>C | CA450608774 | MMUT | c.681T>G (p.Val227=) | dbSNP gnomAD v2 gnomAD v4 |
6 | g.49457763A>G | CA450608776 | MMUT | c.681T>C (p.Val227=) | |
6 | g.49457763A>T | CA450608775 | MMUT | c.681T>A (p.Val227=) | |
6 | g.49457764A>C | CA364404127 | MMUT | c.680T>G (p.Val227Gly) | |
6 | g.49457764A>G | CA364404129 | MMUT | c.680T>C (p.Val227Ala) | |
6 | g.49457764A>T | CA364404131 | MMUT | c.680T>A (p.Val227Asp) | |
6 | g.49457765C>A | CA364404135 | MMUT | c.679G>T (p.Val227Phe) | |
6 | g.49457765C= | CA1627392099 | MMUT | c.679G= (p.Val227=) | |
6 | g.49457765C>G | CA364404137 | MMUT | c.679G>C (p.Val227Leu) | |
6 | g.49457765C>T | CA364404139 | MMUT | c.679G>A (p.Val227Ile) | |
6 | g.49457766dup | CA913110644 | MMUT | c.679dup (p.Val227GlyfsTer18) |