Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
17 | g.47283371A= | CA2262604834 | ITGB3 | c.183A= (p.Ser61=) c.148A= | |
17 | g.47283371A>C | CA500429505 | ITGB3 | c.183A>C (p.Ser61=) c.148A>C | |
17 | g.47283371A>G | CA500429504 | ITGB3 | c.183A>G (p.Ser61=) c.148A>G | ClinVar dbSNP gnomAD v4 |
17 | g.47283371A>T | CA500429506 | ITGB3 | c.183A>T (p.Ser61=) c.148A>T | |
17 | g.47283372C>A | CA400020437 | ITGB3 | c.184C>A (p.Pro62Thr) c.149C>A | gnomAD v4 |
17 | g.47283372C>G | CA400020439 | ITGB3 | c.184C>G (p.Pro62Ala) c.149C>G | gnomAD v4 |
17 | g.47283372C>T | CA400020441 | ITGB3 | c.184C>T (p.Pro62Ser) c.149C>T | gnomAD v4 |
17 | g.47283373C>A | CA400020443 | ITGB3 | c.185C>A (p.Pro62His) c.150C>A | |
17 | g.47283373C>G | CA400020445 | ITGB3 | c.185C>G (p.Pro62Arg) c.150C>G | |
17 | g.47283373C>T | CA400020446 | ITGB3 | c.185C>T (p.Pro62Leu) c.150C>T | |
17 | g.47283374T>A | CA500429507 | ITGB3 | c.186T>A (p.Pro62=) c.151T>A | |
17 | g.47283374T>C | CA500429508 | ITGB3 | c.186T>C (p.Pro62=) c.151T>C | |
17 | g.47283374T>G | CA500429509 | ITGB3 | c.186T>G (p.Pro62=) c.151T>G | |
17 | g.47283375C>A | CA400020448 | ITGB3 | c.187C>A (p.Arg63Ser) c.152C>A | |
17 | g.47283375C= | CA2262604835 | ITGB3 | c.187C= (p.Arg63=) c.152C= | |
17 | g.47283375C>G | CA400020451 | ITGB3 | c.187C>G (p.Arg63Gly) c.152C>G | |
17 | g.47283375C>T | CA8622892 | ITGB3 | c.187C>T (p.Arg63Cys) c.152C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC COSMIC |
17 | g.47283376G>A | CA8622893 | ITGB3 | c.188G>A (p.Arg63His) c.153G>A | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.47283376G>C | CA400020456 | ITGB3 | c.188G>C (p.Arg63Pro) c.153G>C | |
17 | g.47283376G= | CA2262604836 | ITGB3 | c.188G= (p.Arg63=) c.153G= | |
17 | g.47283376G>T | CA400020454 | ITGB3 | c.188G>T (p.Arg63Leu) c.153G>T | |
17 | g.47283377C>A | CA500429510 | ITGB3 | c.189C>A (p.Arg63=) c.154C>A | |
17 | g.47283377C>G | CA500429512 | ITGB3 | c.189C>G (p.Arg63=) c.154C>G | |
17 | g.47283377C>T | CA500429511 | ITGB3 | c.189C>T (p.Arg63=) c.154C>T | |
17 | g.47283378T>A | CA400020458 | ITGB3 | c.190T>A (p.Cys64Ser) c.155T>A | |
17 | g.47283378T>C | CA400020461 | ITGB3 | c.190T>C (p.Cys64Arg) c.155T>C | |
17 | g.47283378T>G | CA400020460 | ITGB3 | c.190T>G (p.Cys64Gly) c.155T>G | |
17 | g.47283379G>A | CA291224490 | ITGB3 | c.191G>A (p.Cys64Tyr) c.156G>A | ClinVar dbSNP |
17 | g.47283379G>C | CA400020463 | ITGB3 | c.191G>C (p.Cys64Ser) c.156G>C | COSMIC COSMIC COSMIC |
17 | g.47283379G= | CA2262604837 | ITGB3 | c.191G= (p.Cys64=) c.156G= | |
17 | g.47283379G>T | CA400020465 | ITGB3 | c.191G>T (p.Cys64Phe) c.156G>T | dbSNP |
17 | g.47283380T>A | CA400020468 | ITGB3 | c.192T>A (p.Cys64Ter) c.157T>A | |
17 | g.47283380T>C | CA500429513 | ITGB3 | c.192T>C (p.Cys64=) c.157T>C | |
17 | g.47283380T>G | CA400020470 | ITGB3 | c.192T>G (p.Cys64Trp) c.157T>G | gnomAD v4 |
17 | g.47283381G>A | CA400020473 | ITGB3 | c.193G>A (p.Asp65Asn) c.158G>A | |
17 | g.47283381G>C | CA400020474 | ITGB3 | c.193G>C (p.Asp65His) c.158G>C | |
17 | g.47283381G>T | CA400020476 | ITGB3 | c.193G>T (p.Asp65Tyr) c.158G>T | |
17 | g.47283382A>C | CA400020479 | ITGB3 | c.194A>C (p.Asp65Ala) c.159A>C | |
17 | g.47283382A>G | CA400020480 | ITGB3 | c.194A>G (p.Asp65Gly) c.159A>G | |
17 | g.47283382A>T | CA400020481 | ITGB3 | c.194A>T (p.Asp65Val) c.159A>T | |
17 | g.47283383C>A | CA400020484 | ITGB3 | c.195C>A (p.Asp65Glu) c.160C>A | |
17 | g.47283383C= | CA2262604838 | ITGB3 | c.195C= (p.Asp65=) c.160C= | |
17 | g.47283383C>G | CA400020486 | ITGB3 | c.195C>G (p.Asp65Glu) c.160C>G | |
17 | g.47283383C>T | CA8622894 | ITGB3 | c.195C>T (p.Asp65=) c.160C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.47283384C>A | CA400020489 | ITGB3 | c.196C>A (p.Leu66Met) c.161C>A | |
17 | g.47283384C>G | CA400020490 | ITGB3 | c.196C>G (p.Leu66Val) c.161C>G | |
17 | g.47283384C>T | CA500429514 | ITGB3 | c.196C>T (p.Leu66=) c.161C>T | |
17 | g.47283385T>A | CA400020494 | ITGB3 | c.197T>A (p.Leu66Gln) c.162T>A | |
17 | g.47283385T>C | CA400020495 | ITGB3 | c.197T>C (p.Leu66Pro) c.162T>C | gnomAD v4 |
17 | g.47283385T>G | CA8622895 | ITGB3 | c.197T>G (p.Leu66Arg) c.162T>G | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |