Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
17 | g.47284512T>A | CA400021927 | ITGB3 | c.431T>A (p.Met144Lys) c.396T>A | gnomAD v4 |
17 | g.47284512T>C | CA400021929 | ITGB3 | c.431T>C (p.Met144Thr) c.396T>C | |
17 | g.47284512T>G | CA291224645 | ITGB3 | c.431T>G (p.Met144Arg) c.396T>G | ClinVar dbSNP gnomAD v3 gnomAD v4 |
17 | g.47284512T= | CA2262605302 | ITGB3 | c.431T= (p.Met144=) c.396T= | |
17 | g.47284513G>A | CA400021937 | ITGB3 | c.432G>A (p.Met144Ile) c.397G>A | COSMIC COSMIC |
17 | g.47284513G>C | CA400021935 | ITGB3 | c.432G>C (p.Met144Ile) c.397G>C | COSMIC COSMIC COSMIC |
17 | g.47284513G>T | CA400021933 | ITGB3 | c.432G>T (p.Met144Ile) c.397G>T | |
17 | g.47284514G>A | CA400021939 | ITGB3 | c.433G>A (p.Asp145Asn) c.398G>A | ClinVar dbSNP |
17 | g.47284514G>C | CA400021940 | ITGB3 | c.433G>C (p.Asp145His) c.398G>C | |
17 | g.47284514G= | CA2262605303 | ITGB3 | c.433G= (p.Asp145=) c.398G= | |
17 | g.47284514G>T | CA123226 | ITGB3 | c.433G>T (p.Asp145Tyr) c.398G>T | ClinVar dbSNP |
17 | g.47284515A>C | CA400021943 | ITGB3 | c.434A>C (p.Asp145Ala) c.399A>C | |
17 | g.47284515A>G | CA400021945 | ITGB3 | c.434A>G (p.Asp145Gly) c.399A>G | |
17 | g.47284515A>T | CA400021947 | ITGB3 | c.434A>T (p.Asp145Val) c.399A>T | |
17 | g.47284516C>A | CA400021950 | ITGB3 | c.435C>A (p.Asp145Glu) c.400C>A | |
17 | g.47284516C>G | CA400021951 | ITGB3 | c.435C>G (p.Asp145Glu) c.400C>G | |
17 | g.47284516C>T | CA500430603 | ITGB3 | c.435C>T (p.Asp145=) c.400C>T | |
17 | g.47284517C>A | CA400021954 | ITGB3 | c.436C>A (p.Leu146Met) c.401C>A | |
17 | g.47284517C>G | CA400021956 | ITGB3 | c.436C>G (p.Leu146Val) c.401C>G | |
17 | g.47284517C>T | CA500430609 | ITGB3 | c.436C>T (p.Leu146=) c.401C>T | gnomAD v4 |
17 | g.47284518T>A | CA400021959 | ITGB3 | c.437T>A (p.Leu146Gln) c.402T>A | |
17 | g.47284518T>C | CA400021960 | ITGB3 | c.437T>C (p.Leu146Pro) c.402T>C | ClinVar dbSNP gnomAD v4 |
17 | g.47284518T>G | CA400021962 | ITGB3 | c.437T>G (p.Leu146Arg) c.402T>G | gnomAD v4 |
17 | g.47284518T= | CA2262605304 | ITGB3 | c.437T= (p.Leu146=) c.402T= | |
17 | g.47284519G>A | CA8622960 | ITGB3 | c.438G>A (p.Leu146=) c.403G>A | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.47284519G>C | CA500430618 | ITGB3 | c.438G>C (p.Leu146=) c.403G>C | |
17 | g.47284519G= | CA2262605305 | ITGB3 | c.438G= (p.Leu146=) c.403G= | |
17 | g.47284519G>T | CA500430620 | ITGB3 | c.438G>T (p.Leu146=) c.403G>T | |
17 | g.47284520T>A | CA400021970 | ITGB3 | c.439T>A (p.Ser147Thr) c.404T>A | |
17 | g.47284520T>C | CA400021968 | ITGB3 | c.439T>C (p.Ser147Pro) c.404T>C | dbSNP |
17 | g.47284520T>G | CA400021966 | ITGB3 | c.439T>G (p.Ser147Ala) c.404T>G | |
17 | g.47284520T= | CA2262605306 | ITGB3 | c.439T= (p.Ser147=) c.404T= | |
17 | g.47284521C>A | CA400021972 | ITGB3 | c.440C>A (p.Ser147Tyr) c.405C>A | |
17 | g.47284521C= | CA2262605307 | ITGB3 | c.440C= (p.Ser147=) c.405C= | |
17 | g.47284521C>G | CA400021974 | ITGB3 | c.440C>G (p.Ser147Cys) c.405C>G | |
17 | g.47284521C>T | CA400021976 | ITGB3 | c.440C>T (p.Ser147Phe) c.405C>T | dbSNP |
17 | g.47284522T>A | CA500430635 | ITGB3 | c.441T>A (p.Ser147=) c.406T>A | |
17 | g.47284522T>C | CA500430638 | ITGB3 | c.441T>C (p.Ser147=) c.406T>C | |
17 | g.47284522T>G | CA500430637 | ITGB3 | c.441T>G (p.Ser147=) c.406T>G | |
17 | g.47284523T>A | CA400021977 | ITGB3 | c.442T>A (p.Tyr148Asn) c.407T>A | |
17 | g.47284523T>C | CA400021979 | ITGB3 | c.442T>C (p.Tyr148His) c.407T>C | |
17 | g.47284523T>G | CA400021981 | ITGB3 | c.442T>G (p.Tyr148Asp) c.407T>G | |
17 | g.47284524A>C | CA400021988 | ITGB3 | c.443A>C (p.Tyr148Ser) c.408A>C | |
17 | g.47284524A>G | CA400021984 | ITGB3 | c.443A>G (p.Tyr148Cys) c.408A>G | |
17 | g.47284524A>T | CA400021986 | ITGB3 | c.443A>T (p.Tyr148Phe) c.408A>T | |
17 | g.47284525del | CA2638435393 | ITGB3 | c.444del (p.Ser149ProfsTer2) c.409del | gnomAD v4 |
17 | g.47284525C>A | CA400021991 | ITGB3 | c.444C>A (p.Tyr148Ter) c.409C>A | |
17 | g.47284525C= | CA2262605308 | ITGB3 | c.444C= (p.Tyr148=) c.409C= | |
17 | g.47284525C>G | CA400021992 | ITGB3 | c.444C>G (p.Tyr148Ter) c.409C>G | ClinVar dbSNP gnomAD v4 |
17 | g.47284525C>T | CA291224647 | ITGB3 | c.444C>T (p.Tyr148=) c.409C>T | ClinVar dbSNP gnomAD v3 gnomAD v4 |