Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
10 | g.17071435_17071437delinsATC | CA1893446920 | CUBN | c.2614_2616delinsGAT (p.Asp872=) | |
10 | g.17071437_17071438del | CA144270 | CUBN | c.2614_2615del (p.Asp872LeufsTer3) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
10 | g.17071437C>A | CA376158688 | CUBN | c.2614G>T (p.Asp872Tyr) | |
10 | g.17071437C>G | CA376158686 | CUBN | c.2614G>C (p.Asp872His) | |
10 | g.17071437C>T | CA376158684 | CUBN | c.2614G>A (p.Asp872Asn) | |
10 | g.17071438T>A | CA468407519 | CUBN | c.2613A>T (p.Thr871=) | dbSNP gnomAD v3 gnomAD v4 |
10 | g.17071438T>C | CA468407521 | CUBN | c.2613A>G (p.Thr871=) | |
10 | g.17071438T>G | CA468407522 | CUBN | c.2613A>C (p.Thr871=) | |
10 | g.17071438T= | CA1893446922 | CUBN | c.2613A= (p.Thr871=) | |
10 | g.17071439G>A | CA376158690 | CUBN | c.2612C>T (p.Thr871Ile) | |
10 | g.17071439G>C | CA376158692 | CUBN | c.2612C>G (p.Thr871Arg) | |
10 | g.17071439G>T | CA376158694 | CUBN | c.2612C>A (p.Thr871Lys) | |
10 | g.17071440T>A | CA376158696 | CUBN | c.2611A>T (p.Thr871Ser) | |
10 | g.17071440T>C | CA376158708 | CUBN | c.2611A>G (p.Thr871Ala) | dbSNP |
10 | g.17071440T>G | CA376158717 | CUBN | c.2611A>C (p.Thr871Pro) | |
10 | g.17071440T= | CA1893446923 | CUBN | c.2611A= (p.Thr871=) | |
10 | g.17071441T>A | CA5424935 | CUBN | c.2610A>T (p.Glu870Asp) | dbSNP ExAC |
10 | g.17071441T>C | CA5424934 | CUBN | c.2610A>G (p.Glu870=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
10 | g.17071441T>G | CA376158734 | CUBN | c.2610A>C (p.Glu870Asp) | |
10 | g.17071441T= | CA1893446925 | CUBN | c.2610A= (p.Glu870=) | |
10 | g.17071442T>A | CA376158744 | CUBN | c.2609A>T (p.Glu870Val) | |
10 | g.17071442T>C | CA376158746 | CUBN | c.2609A>G (p.Glu870Gly) | |
10 | g.17071442T>G | CA376158748 | CUBN | c.2609A>C (p.Glu870Ala) | |
10 | g.17071442_17071445del | CA2608401144 | CUBN | c.2606_2609del (p.Cys869Ter) | gnomAD v4 |
10 | g.17071443C>A | CA376158752 | CUBN | c.2608G>T (p.Glu870Ter) | |
10 | g.17071443C>G | CA376158758 | CUBN | c.2608G>C (p.Glu870Gln) | |
10 | g.17071443C>T | CA376158754 | CUBN | c.2608G>A (p.Glu870Lys) | |
10 | g.17071444A>C | CA376158760 | CUBN | c.2607T>G (p.Cys869Trp) | |
10 | g.17071444A>G | CA468407528 | CUBN | c.2607T>C (p.Cys869=) | |
10 | g.17071444A>T | CA376158763 | CUBN | c.2607T>A (p.Cys869Ter) | |
10 | g.17071445C>A | CA376158764 | CUBN | c.2606G>T (p.Cys869Phe) | gnomAD v4 |
10 | g.17071445C>G | CA376158766 | CUBN | c.2606G>C (p.Cys869Ser) | |
10 | g.17071445C>T | CA376158769 | CUBN | c.2606G>A (p.Cys869Tyr) | |
10 | g.17071446A>C | CA376158771 | CUBN | c.2605T>G (p.Cys869Gly) | |
10 | g.17071446A>G | CA376158774 | CUBN | c.2605T>C (p.Cys869Arg) | gnomAD v4 |
10 | g.17071446A>T | CA376158783 | CUBN | c.2605T>A (p.Cys869Ser) | |
10 | g.17071447G>A | CA468407531 | CUBN | c.2604C>T (p.His868=) | |
10 | g.17071447G>C | CA376158785 | CUBN | c.2604C>G (p.His868Gln) | |
10 | g.17071447G>T | CA376158786 | CUBN | c.2604C>A (p.His868Gln) | |
10 | g.17071448T>A | CA376158787 | CUBN | c.2603A>T (p.His868Leu) | |
10 | g.17071448T>C | CA376158790 | CUBN | c.2603A>G (p.His868Arg) | dbSNP |
10 | g.17071448T>G | CA376158791 | CUBN | c.2603A>C (p.His868Pro) | |
10 | g.17071448T= | CA1893446928 | CUBN | c.2603A= (p.His868=) | |
10 | g.17071449G>A | CA376158794 | CUBN | c.2602C>T (p.His868Tyr) | dbSNP |
10 | g.17071449G>C | CA376158801 | CUBN | c.2602C>G (p.His868Asp) | |
10 | g.17071449G= | CA1893446929 | CUBN | c.2602C= (p.His868=) | |
10 | g.17071449G>T | CA376158802 | CUBN | c.2602C>A (p.His868Asn) | |
10 | g.17071450G>A | CA468407533 | CUBN | c.2601C>T (p.Ala867=) | |
10 | g.17071450G>C | CA468407535 | CUBN | c.2601C>G (p.Ala867=) | |
10 | g.17071450G>T | CA468407536 | CUBN | c.2601C>A (p.Ala867=) |