Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
17 | g.47286294A>C | CA400023435 | ITGB3 | c.649A>C (p.Lys217Gln) c.614A>C | |
17 | g.47286294A>G | CA400023436 | ITGB3 | c.649A>G (p.Lys217Glu) c.614A>G | gnomAD v4 |
17 | g.47286294A>T | CA400023437 | ITGB3 | c.649A>T (p.Lys217Ter) c.614A>T | |
17 | g.47286295A>C | CA400023438 | ITGB3 | c.650A>C (p.Lys217Thr) c.615A>C | |
17 | g.47286295A>G | CA400023439 | ITGB3 | c.650A>G (p.Lys217Arg) c.615A>G | |
17 | g.47286295A>T | CA400023440 | ITGB3 | c.650A>T (p.Lys217Ile) c.615A>T | |
17 | g.47286296A= | CA2262605985 | ITGB3 | c.651A= (p.Lys217=) c.616A= | |
17 | g.47286296A>C | CA400023441 | ITGB3 | c.651A>C (p.Lys217Asn) c.616A>C | |
17 | g.47286296A>G | CA500431969 | ITGB3 | c.651A>G (p.Lys217=) c.616A>G | dbSNP gnomAD v3 gnomAD v4 |
17 | g.47286296A>T | CA400023442 | ITGB3 | c.651A>T (p.Lys217Asn) c.616A>T | gnomAD v4 |
17 | g.47286297C>A | CA400023443 | ITGB3 | c.652C>A (p.His218Asn) c.617C>A | |
17 | g.47286297C>G | CA400023444 | ITGB3 | c.652C>G (p.His218Asp) c.617C>G | |
17 | g.47286297C>T | CA400023445 | ITGB3 | c.652C>T (p.His218Tyr) c.617C>T | ClinVar dbSNP |
17 | g.47286298A>C | CA400023447 | ITGB3 | c.653A>C (p.His218Pro) c.618A>C | |
17 | g.47286298A>G | CA400023448 | ITGB3 | c.653A>G (p.His218Arg) c.618A>G | gnomAD v4 |
17 | g.47286298A>T | CA400023446 | ITGB3 | c.653A>T (p.His218Leu) c.618A>T | |
17 | g.47286299C>A | CA400023450 | ITGB3 | c.654C>A (p.His218Gln) c.619C>A | |
17 | g.47286299C= | CA2262605986 | ITGB3 | c.654C= (p.His218=) c.619C= | |
17 | g.47286299C>G | CA400023449 | ITGB3 | c.654C>G (p.His218Gln) c.619C>G | |
17 | g.47286299C>T | CA8623015 | ITGB3 | c.654C>T (p.His218=) c.619C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.47286300G>A | CA8623016 | ITGB3 | c.655G>A (p.Val219Met) c.620G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
17 | g.47286300G>C | CA400023452 | ITGB3 | c.655G>C (p.Val219Leu) c.620G>C | gnomAD v4 |
17 | g.47286300G= | CA2262605987 | ITGB3 | c.655G= (p.Val219=) c.620G= | |
17 | g.47286300G>T | CA400023451 | ITGB3 | c.655G>T (p.Val219Leu) c.620G>T | gnomAD v4 |
17 | g.47286301T>A | CA400023453 | ITGB3 | c.656T>A (p.Val219Glu) c.621T>A | |
17 | g.47286301T>C | CA400023455 | ITGB3 | c.656T>C (p.Val219Ala) c.621T>C | dbSNP gnomAD v3 gnomAD v4 |
17 | g.47286301T>G | CA400023454 | ITGB3 | c.656T>G (p.Val219Gly) c.621T>G | |
17 | g.47286301T= | CA2262605988 | ITGB3 | c.656T= (p.Val219=) c.621T= | |
17 | g.47286302G>A | CA500431972 | ITGB3 | c.657G>A (p.Val219=) c.622G>A | |
17 | g.47286302G>C | CA500431971 | ITGB3 | c.657G>C (p.Val219=) c.622G>C | gnomAD v4 |
17 | g.47286302G>T | CA500431970 | ITGB3 | c.657G>T (p.Val219=) c.622G>T | |
17 | g.47286303C>A | CA400023456 | ITGB3 | c.658C>A (p.Leu220Met) c.623C>A | |
17 | g.47286303C>G | CA400023457 | ITGB3 | c.658C>G (p.Leu220Val) c.623C>G | |
17 | g.47286303C>T | CA500431973 | ITGB3 | c.658C>T (p.Leu220=) c.623C>T | |
17 | g.47286304T>A | CA400023458 | ITGB3 | c.659T>A (p.Leu220Gln) c.624T>A | gnomAD v4 |
17 | g.47286304T>C | CA400023459 | ITGB3 | c.659T>C (p.Leu220Pro) c.624T>C | |
17 | g.47286304T>G | CA400023460 | ITGB3 | c.659T>G (p.Leu220Arg) c.624T>G | |
17 | g.47286305G>A | CA500431975 | ITGB3 | c.660G>A (p.Leu220=) c.625G>A | |
17 | g.47286305G>C | CA500431974 | ITGB3 | c.660G>C (p.Leu220=) c.625G>C | |
17 | g.47286305G>T | CA500431976 | ITGB3 | c.660G>T (p.Leu220=) c.625G>T | |
17 | g.47286306A>C | CA400023461 | ITGB3 | c.661A>C (p.Thr221Pro) c.626A>C | |
17 | g.47286306A>G | CA400023462 | ITGB3 | c.661A>G (p.Thr221Ala) c.626A>G | |
17 | g.47286306A>T | CA400023463 | ITGB3 | c.661A>T (p.Thr221Ser) c.626A>T | |
17 | g.47286307C>A | CA400023464 | ITGB3 | c.662C>A (p.Thr221Lys) c.627C>A | |
17 | g.47286307C= | CA2262605989 | ITGB3 | c.662C= (p.Thr221=) c.627C= | |
17 | g.47286307C>G | CA400023465 | ITGB3 | c.662C>G (p.Thr221Arg) c.627C>G | gnomAD v4 |
17 | g.47286307C>T | CA8623017 | ITGB3 | c.662C>T (p.Thr221Met) c.627C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.47286308G>A | CA8623018 | ITGB3 | c.663G>A (p.Thr221=) c.628G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.47286308G>C | CA500431977 | ITGB3 | c.663G>C (p.Thr221=) c.628G>C | |
17 | g.47286308G= | CA2262605990 | ITGB3 | c.663G= (p.Thr221=) c.628G= |