| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| Y | g.12726767C>A | CA414981956 | USP9Y | c.631C>A (p.Arg211Ser) n.643C>A c.397C>A (p.Arg133Ser) | |
| Y | g.12726767C= | CA2470554869 | USP9Y | c.631C= (p.Arg211=) n.643C= c.397C= (p.Arg133=) | |
| Y | g.12726767C>G | CA414981957 | USP9Y | c.631C>G (p.Arg211Gly) n.643C>G c.397C>G (p.Arg133Gly) | |
| Y | g.12726767C>T | CA10573053 | USP9Y | c.631C>T (p.Arg211Cys) n.643C>T c.397C>T (p.Arg133Cys) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| Y | g.12726768G>A | CA414981958 | USP9Y | c.632G>A (p.Arg211His) n.644G>A c.398G>A (p.Arg133His) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| Y | g.12726768G>C | CA414981959 | USP9Y | c.632G>C (p.Arg211Pro) n.644G>C c.398G>C (p.Arg133Pro) | |
| Y | g.12726768G= | CA2470554870 | USP9Y | c.632G= (p.Arg211=) n.644G= c.398G= (p.Arg133=) | |
| Y | g.12726768G>T | CA414981960 | USP9Y | c.632G>T (p.Arg211Leu) n.644G>T c.398G>T (p.Arg133Leu) | |
| Y | g.12726769T>A | CA519863277 | USP9Y | c.633T>A (p.Arg211=) n.645T>A c.399T>A (p.Arg133=) | |
| Y | g.12726769T>C | CA519863280 | USP9Y | c.633T>C (p.Arg211=) n.645T>C c.399T>C (p.Arg133=) | |
| Y | g.12726769T>G | CA519863283 | USP9Y | c.633T>G (p.Arg211=) n.645T>G c.399T>G (p.Arg133=) | |
| Y | g.12726770T>A | CA414981963 | USP9Y | c.634T>A (p.Ser212Thr) n.646T>A c.400T>A (p.Ser134Thr) | |
| Y | g.12726770T>C | CA414981961 | USP9Y | c.634T>C (p.Ser212Pro) n.646T>C c.400T>C (p.Ser134Pro) | |
| Y | g.12726770T>G | CA414981962 | USP9Y | c.634T>G (p.Ser212Ala) n.646T>G c.400T>G (p.Ser134Ala) | |
| Y | g.12726771C>A | CA414981964 | USP9Y | c.635C>A (p.Ser212Tyr) n.647C>A c.401C>A (p.Ser134Tyr) | |
| Y | g.12726771C>G | CA414981965 | USP9Y | c.635C>G (p.Ser212Cys) n.647C>G c.401C>G (p.Ser134Cys) | |
| Y | g.12726771C>T | CA414981966 | USP9Y | c.635C>T (p.Ser212Phe) n.647C>T c.401C>T (p.Ser134Phe) | |
| Y | g.12726772T>A | CA519863297 | USP9Y | c.636T>A (p.Ser212=) n.648T>A c.402T>A (p.Ser134=) | |
| Y | g.12726772T>C | CA519863300 | USP9Y | c.636T>C (p.Ser212=) n.648T>C c.402T>C (p.Ser134=) | |
| Y | g.12726772T>G | CA519863304 | USP9Y | c.636T>G (p.Ser212=) n.648T>G c.402T>G (p.Ser134=) | |
| Y | g.12726773T>A | CA414981967 | USP9Y | c.637T>A (p.Ser213Thr) n.649T>A c.403T>A (p.Ser135Thr) | |
| Y | g.12726773T>C | CA414981968 | USP9Y | c.637T>C (p.Ser213Pro) n.649T>C c.403T>C (p.Ser135Pro) | |
| Y | g.12726773T>G | CA414981969 | USP9Y | c.637T>G (p.Ser213Ala) n.649T>G c.403T>G (p.Ser135Ala) | |
| Y | g.12726774C>A | CA414981970 | USP9Y | c.638C>A (p.Ser213Ter) n.650C>A c.404C>A (p.Ser135Ter) | |
| Y | g.12726774C>G | CA414981971 | USP9Y | c.638C>G (p.Ser213Ter) n.650C>G c.404C>G (p.Ser135Ter) | |
| Y | g.12726774C>T | CA414981972 | USP9Y | c.638C>T (p.Ser213Leu) n.650C>T c.404C>T (p.Ser135Leu) | |
| Y | g.12726775A= | CA2470554871 | USP9Y | c.639A= (p.Ser213=) n.651A= c.405A= (p.Ser135=) | |
| Y | g.12726775A>C | CA519863323 | USP9Y | c.639A>C (p.Ser213=) n.651A>C c.405A>C (p.Ser135=) | |
| Y | g.12726775A>G | CA519863326 | USP9Y | c.639A>G (p.Ser213=) n.651A>G c.405A>G (p.Ser135=) | dbSNP gnomAD v3 gnomAD v4 |
| Y | g.12726775A>T | CA519863328 | USP9Y | c.639A>T (p.Ser213=) n.651A>T c.405A>T (p.Ser135=) | gnomAD v3 gnomAD v4 |
| Y | g.12726776G>A | CA414981973 | USP9Y | c.640G>A (p.Asp214Asn) n.652G>A c.406G>A (p.Asp136Asn) | |
| Y | g.12726776G>C | CA414981974 | USP9Y | c.640G>C (p.Asp214His) n.652G>C c.406G>C (p.Asp136His) | |
| Y | g.12726776G>T | CA414981975 | USP9Y | c.640G>T (p.Asp214Tyr) n.652G>T c.406G>T (p.Asp136Tyr) | |
| Y | g.12726777A>C | CA414981976 | USP9Y | c.641A>C (p.Asp214Ala) n.653A>C c.407A>C (p.Asp136Ala) | |
| Y | g.12726777A>G | CA414981978 | USP9Y | c.641A>G (p.Asp214Gly) n.653A>G c.407A>G (p.Asp136Gly) | |
| Y | g.12726777A>T | CA414981977 | USP9Y | c.641A>T (p.Asp214Val) n.653A>T c.407A>T (p.Asp136Val) | |
| Y | g.12726778T>A | CA414981979 | USP9Y | c.642T>A (p.Asp214Glu) n.654T>A c.408T>A (p.Asp136Glu) | |
| Y | g.12726778T>C | CA519863347 | USP9Y | c.642T>C (p.Asp214=) n.654T>C c.408T>C (p.Asp136=) | |
| Y | g.12726778T>G | CA414981980 | USP9Y | c.642T>G (p.Asp214Glu) n.654T>G c.408T>G (p.Asp136Glu) | |
| Y | g.12726779C>A | CA414981981 | USP9Y | c.643C>A (p.Pro215Thr) n.655C>A c.409C>A (p.Pro137Thr) | |
| Y | g.12726779C>G | CA414981982 | USP9Y | c.643C>G (p.Pro215Ala) n.655C>G c.409C>G (p.Pro137Ala) | |
| Y | g.12726779C>T | CA414981983 | USP9Y | c.643C>T (p.Pro215Ser) n.655C>T c.409C>T (p.Pro137Ser) | |
| Y | g.12726780C>A | CA414981984 | USP9Y | c.644C>A (p.Pro215His) n.656C>A c.410C>A (p.Pro137His) | |
| Y | g.12726780C>G | CA414981985 | USP9Y | c.644C>G (p.Pro215Arg) n.656C>G c.410C>G (p.Pro137Arg) | |
| Y | g.12726780C>T | CA414981986 | USP9Y | c.644C>T (p.Pro215Leu) n.656C>T c.410C>T (p.Pro137Leu) | |
| Y | g.12726781T>A | CA519863366 | USP9Y | c.645T>A (p.Pro215=) n.657T>A c.411T>A (p.Pro137=) | |
| Y | g.12726781T>C | CA519863368 | USP9Y | c.645T>C (p.Pro215=) n.657T>C c.411T>C (p.Pro137=) | |
| Y | g.12726781T>G | CA519863370 | USP9Y | c.645T>G (p.Pro215=) n.657T>G c.411T>G (p.Pro137=) | |
| Y | g.12726782C>A | CA519863382 | USP9Y | c.646C>A (p.Arg216=) n.658C>A c.412C>A (p.Arg138=) | |
| Y | g.12726782C= | CA2470554872 | USP9Y | c.646C= (p.Arg216=) n.658C= c.412C= (p.Arg138=) |