Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
X | g.41136893C>A | CA515966423 | USP9X | c.525C>A (p.Ala175=) | ClinVar |
X | g.41136893C= | CA2425806605 | USP9X | c.525C= (p.Ala175=) | |
X | g.41136893C>G | CA10388324 | USP9X | c.525C>G (p.Ala175=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
X | g.41136893C>T | CA515966424 | USP9X | c.525C>T (p.Ala175=) | |
X | g.41136894A= | CA2425806606 | USP9X | c.526A= (p.Met176=) | |
X | g.41136894A>C | CA412763094 | USP9X | c.526A>C (p.Met176Leu) | |
X | g.41136894A>G | CA412763098 | USP9X | c.526A>G (p.Met176Val) | |
X | g.41136894A>T | CA412763100 | USP9X | c.526A>T (p.Met176Leu) | dbSNP gnomAD v4 |
X | g.41136895T>A | CA412763110 | USP9X | c.527T>A (p.Met176Lys) | |
X | g.41136895T>C | CA412763104 | USP9X | c.527T>C (p.Met176Thr) | dbSNP gnomAD v2 gnomAD v4 |
X | g.41136895T>G | CA412763108 | USP9X | c.527T>G (p.Met176Arg) | |
X | g.41136895T= | CA2425806607 | USP9X | c.527T= (p.Met176=) | |
X | g.41136896G>A | CA412763115 | USP9X | c.528G>A (p.Met176Ile) | |
X | g.41136896G>C | CA412763119 | USP9X | c.528G>C (p.Met176Ile) | |
X | g.41136896G>T | CA412763116 | USP9X | c.528G>T (p.Met176Ile) | |
X | g.41136897G>A | CA412763124 | USP9X | c.529G>A (p.Ala177Thr) | gnomAD v4 |
X | g.41136897G>C | CA412763128 | USP9X | c.529G>C (p.Ala177Pro) | |
X | g.41136897G>T | CA412763126 | USP9X | c.529G>T (p.Ala177Ser) | |
X | g.41136898C>A | CA412763131 | USP9X | c.530C>A (p.Ala177Asp) | |
X | g.41136898C>G | CA412763137 | USP9X | c.530C>G (p.Ala177Gly) | |
X | g.41136898C>T | CA412763134 | USP9X | c.530C>T (p.Ala177Val) | gnomAD v4 |
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=) |