Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
X | g.41136899C>A | CA515966436 | USP9X | c.531C>A (p.Ala177=) | |
X | g.41136899C>G | CA515966437 | USP9X | c.531C>G (p.Ala177=) | |
X | g.41136899C>T | CA515966438 | USP9X | c.531C>T (p.Ala177=) | gnomAD v4 |
X | g.41136900T>A | CA412763139 | USP9X | c.532T>A (p.Leu178Ile) | |
X | g.41136900T>C | CA515966439 | USP9X | c.532T>C (p.Leu178=) | |
X | g.41136900T>G | CA412763142 | USP9X | c.532T>G (p.Leu178Val) | |
X | g.41136901T>A | CA412763145 | USP9X | c.533T>A (p.Leu178Ter) | |
X | g.41136901T>C | CA412763148 | USP9X | c.533T>C (p.Leu178Ser) | |
X | g.41136901T>G | CA412763151 | USP9X | c.533T>G (p.Leu178Ter) | |
X | g.41136902A>C | CA412763154 | USP9X | c.534A>C (p.Leu178Phe) | |
X | g.41136902A>G | CA515966442 | USP9X | c.534A>G (p.Leu178=) | |
X | g.41136902A>T | CA412763156 | USP9X | c.534A>T (p.Leu178Phe) | |
X | g.41136903A>C | CA412763160 | USP9X | c.535A>C (p.Asn179His) | COSMIC |
X | g.41136903A>G | CA412763163 | USP9X | c.535A>G (p.Asn179Asp) | |
X | g.41136903A>T | CA412763165 | USP9X | c.535A>T (p.Asn179Tyr) | |
X | g.41136904A= | CA2425806608 | USP9X | c.536A= (p.Asn179=) | |
X | g.41136904A>C | CA412763167 | USP9X | c.536A>C (p.Asn179Thr) | |
X | g.41136904A>G | CA412763169 | USP9X | c.536A>G (p.Asn179Ser) | dbSNP gnomAD v2 gnomAD v4 COSMIC COSMIC |
X | g.41136904A>T | CA412763171 | USP9X | c.536A>T (p.Asn179Ile) | |
X | g.41136905T>A | CA412763173 | USP9X | c.537T>A (p.Asn179Lys) | |
X | g.41136905T>C | CA515966455 | USP9X | c.537T>C (p.Asn179=) | |
X | g.41136905T>G | CA412763175 | USP9X | c.537T>G (p.Asn179Lys) | |
X | g.41136906C>A | CA412763177 | USP9X | c.538C>A (p.Pro180Thr) | ClinVar dbSNP |
X | g.41136906C>G | CA412763178 | USP9X | c.538C>G (p.Pro180Ala) | |
X | g.41136906C>T | CA412763179 | USP9X | c.538C>T (p.Pro180Ser) | |
X | g.41136907C>A | CA412763180 | USP9X | c.539C>A (p.Pro180His) | |
X | g.41136907C>G | CA412763183 | USP9X | c.539C>G (p.Pro180Arg) | |
X | g.41136907C>T | CA412763184 | USP9X | c.539C>T (p.Pro180Leu) | |
X | g.41136908T>A | CA515966460 | USP9X | c.540T>A (p.Pro180=) | |
X | g.41136908T>C | CA515966465 | USP9X | c.540T>C (p.Pro180=) | |
X | g.41136908T>G | CA515966467 | USP9X | c.540T>G (p.Pro180=) | |
X | g.41136909C>A | CA412763187 | USP9X | c.541C>A (p.His181Asn) | |
X | g.41136909C>G | CA412763188 | USP9X | c.541C>G (p.His181Asp) | |
X | g.41136909C>T | CA412763190 | USP9X | c.541C>T (p.His181Tyr) | gnomAD v4 |
X | g.41136910A= | CA2425806609 | USP9X | c.542A= (p.His181=) | |
X | g.41136910A>C | CA412763192 | USP9X | c.542A>C (p.His181Pro) | |
X | g.41136910A>G | CA412763193 | USP9X | c.542A>G (p.His181Arg) | |
X | g.41136910A>T | CA412763194 | USP9X | c.542A>T (p.His181Leu) | ClinVar dbSNP |
X | g.41136911T>A | CA412763197 | USP9X | c.543T>A (p.His181Gln) | |
X | g.41136911T>C | CA515966470 | USP9X | c.543T>C (p.His181=) | dbSNP |
X | g.41136911T>G | CA412763199 | USP9X | c.543T>G (p.His181Gln) | |
X | g.41136912T>A | CA412763202 | USP9X | c.544T>A (p.Cys182Ser) | |
X | g.41136912T>C | CA412763203 | USP9X | c.544T>C (p.Cys182Arg) | |
X | g.41136912T>G | CA412763206 | USP9X | c.544T>G (p.Cys182Gly) | |
X | g.41136913G>A | CA412763209 | USP9X | c.545G>A (p.Cys182Tyr) | COSMIC COSMIC |
X | g.41136913G>C | CA412763211 | USP9X | c.545G>C (p.Cys182Ser) | |
X | g.41136913G>T | CA412763213 | USP9X | c.545G>T (p.Cys182Phe) | |
X | g.41136914C>A | CA412763218 | USP9X | c.546C>A (p.Cys182Ter) | |
X | g.41136914C>G | CA412763216 | USP9X | c.546C>G (p.Cys182Trp) | gnomAD v4 |
X | g.41136914C>T | CA515966479 | USP9X | c.546C>T (p.Cys182=) |