Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
4 | g.67581431C>A | CA357051674 | STAP1 | c.490C>A (p.Pro164Thr) n.548C>A | gnomAD v4 |
4 | g.67581431C>G | CA357051681 | STAP1 | c.490C>G (p.Pro164Ala) n.548C>G | |
4 | g.67581431C>T | CA357051690 | STAP1 | c.490C>T (p.Pro164Ser) n.548C>T | |
4 | g.67581432C>A | CA357051700 | STAP1 | c.491C>A (p.Pro164Gln) n.549C>A | dbSNP |
4 | g.67581432C= | CA1465349628 | STAP1 | c.491C= (p.Pro164=) n.549C= | |
4 | g.67581432C>G | CA357051693 | STAP1 | c.491C>G (p.Pro164Arg) n.549C>G | |
4 | g.67581432C>T | CA357051695 | STAP1 | c.491C>T (p.Pro164Leu) n.549C>T | dbSNP gnomAD v3 gnomAD v4 |
4 | g.67581433A>C | CA439648623 | STAP1 | c.492A>C (p.Pro164=) n.550A>C | |
4 | g.67581433A>G | CA439648625 | STAP1 | c.492A>G (p.Pro164=) n.550A>G | gnomAD v4 |
4 | g.67581433A>T | CA439648627 | STAP1 | c.492A>T (p.Pro164=) n.550A>T | |
4 | g.67581434A= | CA1465349629 | STAP1 | c.493A= (p.Thr165=) n.551A= | |
4 | g.67581434A>C | CA357051706 | STAP1 | c.493A>C (p.Thr165Pro) n.551A>C | |
4 | g.67581434A>G | CA357051709 | STAP1 | c.493A>G (p.Thr165Ala) n.551A>G | dbSNP gnomAD v4 |
4 | g.67581434A>T | CA357051711 | STAP1 | c.493A>T (p.Thr165Ser) n.551A>T | |
4 | g.67581435C>A | CA357051716 | STAP1 | c.494C>A (p.Thr165Asn) n.552C>A | |
4 | g.67581435C= | CA1465349630 | STAP1 | c.494C= (p.Thr165=) n.552C= | |
4 | g.67581435C>G | CA357051725 | STAP1 | c.494C>G (p.Thr165Ser) n.552C>G | |
4 | g.67581435C>T | CA2937578 | STAP1 | c.494C>T (p.Thr165Ile) n.552C>T | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
4 | g.67581436T>A | CA439648632 | STAP1 | c.495T>A (p.Thr165=) n.553T>A | |
4 | g.67581436T>C | CA439648633 | STAP1 | c.495T>C (p.Thr165=) n.553T>C | |
4 | g.67581436T>G | CA439648635 | STAP1 | c.495T>G (p.Thr165=) n.553T>G | COSMIC |
4 | g.67581437G>A | CA357051733 | STAP1 | c.496G>A (p.Glu166Lys) n.554G>A | |
4 | g.67581437G>C | CA357051735 | STAP1 | c.496G>C (p.Glu166Gln) n.554G>C | |
4 | g.67581437G>T | CA357051747 | STAP1 | c.496G>T (p.Glu166Ter) n.554G>T | |
4 | g.67581438A>C | CA357051752 | STAP1 | c.497A>C (p.Glu166Ala) n.555A>C | |
4 | g.67581438A>G | CA357051763 | STAP1 | c.497A>G (p.Glu166Gly) n.555A>G | |
4 | g.67581438A>T | CA357051767 | STAP1 | c.497A>T (p.Glu166Val) n.555A>T | |
4 | g.67581439A= | CA1465349631 | STAP1 | c.498A= (p.Glu166=) n.556A= | |
4 | g.67581439A>C | CA2937579 | STAP1 | c.498A>C (p.Glu166Asp) n.556A>C | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
4 | g.67581439A>G | CA2937580 | STAP1 | c.498A>G (p.Glu166=) n.556A>G | dbSNP ExAC gnomAD v2 gnomAD v4 |
4 | g.67581439A>T | CA357051775 | STAP1 | c.498A>T (p.Glu166Asp) n.556A>T | |
4 | g.67581440G>A | CA357051783 | STAP1 | c.499G>A (p.Asp167Asn) n.557G>A | gnomAD v4 |
4 | g.67581440G>C | CA357051791 | STAP1 | c.499G>C (p.Asp167His) n.557G>C | |
4 | g.67581440G>T | CA357051793 | STAP1 | c.499G>T (p.Asp167Tyr) n.557G>T | |
4 | g.67581441A= | CA1465349632 | STAP1 | c.500A= (p.Asp167=) n.558A= | |
4 | g.67581441A>C | CA357051806 | STAP1 | c.500A>C (p.Asp167Ala) n.558A>C | |
4 | g.67581441A>G | CA357051809 | STAP1 | c.500A>G (p.Asp167Gly) n.558A>G | |
4 | g.67581441A>T | CA2937581 | STAP1 | c.500A>T (p.Asp167Val) n.558A>T | dbSNP ExAC gnomAD v2 gnomAD v4 |
4 | g.67581442T>A | CA357051815 | STAP1 | c.501T>A (p.Asp167Glu) n.559T>A | |
4 | g.67581442T>C | CA439648647 | STAP1 | c.501T>C (p.Asp167=) n.559T>C | dbSNP gnomAD v4 |
4 | g.67581442T>G | CA357051819 | STAP1 | c.501T>G (p.Asp167Glu) n.559T>G | gnomAD v4 |
4 | g.67581442T= | CA1465349633 | STAP1 | c.501T= (p.Asp167=) n.559T= | |
4 | g.67581443T>A | CA357051823 | STAP1 | c.502T>A (p.Tyr168Asn) n.560T>A | |
4 | g.67581443T>C | CA98655465 | STAP1 | c.502T>C (p.Tyr168His) n.560T>C | dbSNP gnomAD v4 |
4 | g.67581443T>G | CA357051828 | STAP1 | c.502T>G (p.Tyr168Asp) n.560T>G | |
4 | g.67581443T= | CA1465349634 | STAP1 | c.502T= (p.Tyr168=) n.560T= | |
4 | g.67581444A= | CA1465349635 | STAP1 | c.503A= (p.Tyr168=) n.561A= | |
4 | g.67581444A>C | CA2937582 | STAP1 | c.503A>C (p.Tyr168Ser) n.561A>C | dbSNP ExAC gnomAD v2 gnomAD v4 |
4 | g.67581444A>G | CA357051835 | STAP1 | c.503A>G (p.Tyr168Cys) n.561A>G | |
4 | g.67581444A>T | CA357051838 | STAP1 | c.503A>T (p.Tyr168Phe) n.561A>T | gnomAD v4 |