Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
17 | g.41586338A>C | CA399481826 | KRT14 | c.497T>G (p.Phe166Cys) | |
17 | g.41586338A>G | CA399481824 | KRT14 | c.497T>C (p.Phe166Ser) | gnomAD v4 |
17 | g.41586338A>T | CA399481822 | KRT14 | c.497T>A (p.Phe166Tyr) | |
17 | g.41586339A>C | CA399481828 | KRT14 | c.496T>G (p.Phe166Val) | |
17 | g.41586339A>G | CA399481830 | KRT14 | c.496T>C (p.Phe166Leu) | |
17 | g.41586339A>T | CA399481833 | KRT14 | c.496T>A (p.Phe166Ile) | |
17 | g.41586340G>A | CA499991702 | KRT14 | c.495C>T (p.Tyr165=) | |
17 | g.41586340G>C | CA399481835 | KRT14 | c.495C>G (p.Tyr165Ter) | |
17 | g.41586340G>T | CA399481836 | KRT14 | c.495C>A (p.Tyr165Ter) | |
17 | g.41586341T>A | CA399481839 | KRT14 | c.494A>T (p.Tyr165Phe) | dbSNP gnomAD v2 gnomAD v4 |
17 | g.41586341T>C | CA399481842 | KRT14 | c.494A>G (p.Tyr165Cys) | |
17 | g.41586341T>G | CA399481844 | KRT14 | c.494A>C (p.Tyr165Ser) | |
17 | g.41586341T= | CA2260086771 | KRT14 | c.494A= (p.Tyr165=) | |
17 | g.41586342A>C | CA399481846 | KRT14 | c.493T>G (p.Tyr165Asp) | |
17 | g.41586342A>G | CA399481849 | KRT14 | c.493T>C (p.Tyr165His) | |
17 | g.41586342A>T | CA399481851 | KRT14 | c.493T>A (p.Tyr165Asn) | |
17 | g.41586343G>A | CA499991714 | KRT14 | c.492C>T (p.Pro164=) | gnomAD v4 |
17 | g.41586343G>C | CA499991717 | KRT14 | c.492C>G (p.Pro164=) | gnomAD v4 |
17 | g.41586343G>T | CA499991715 | KRT14 | c.492C>A (p.Pro164=) | |
17 | g.41586344G>A | CA399481855 | KRT14 | c.491C>T (p.Pro164Leu) | gnomAD v4 |
17 | g.41586344G>C | CA399481857 | KRT14 | c.491C>G (p.Pro164Arg) | |
17 | g.41586344G>T | CA399481860 | KRT14 | c.491C>A (p.Pro164His) | |
17 | g.41586345G>A | CA399481864 | KRT14 | c.490C>T (p.Pro164Ser) | |
17 | g.41586345G>C | CA399481866 | KRT14 | c.490C>G (p.Pro164Ala) | |
17 | g.41586345G>T | CA399481862 | KRT14 | c.490C>A (p.Pro164Thr) | gnomAD v4 |
17 | g.41586346A>C | CA399481869 | KRT14 | c.489T>G (p.Ser163Arg) | |
17 | g.41586346A>G | CA499991730 | KRT14 | c.489T>C (p.Ser163=) | |
17 | g.41586346A>T | CA399481871 | KRT14 | c.489T>A (p.Ser163Arg) | |
17 | g.41586347C>A | CA399481873 | KRT14 | c.488G>T (p.Ser163Ile) | |
17 | g.41586347C>G | CA399481875 | KRT14 | c.488G>C (p.Ser163Thr) | |
17 | g.41586347C>T | CA399481877 | KRT14 | c.488G>A (p.Ser163Asn) | gnomAD v4 |
17 | g.41586348T>A | CA399481880 | KRT14 | c.487A>T (p.Ser163Cys) | |
17 | g.41586348T>C | CA399481883 | KRT14 | c.487A>G (p.Ser163Gly) | |
17 | g.41586348T>G | CA399481886 | KRT14 | c.487A>C (p.Ser163Arg) | |
17 | g.41586349G>A | CA499991744 | KRT14 | c.486C>T (p.Tyr162=) | gnomAD v4 |
17 | g.41586349G>C | CA399481888 | KRT14 | c.486C>G (p.Tyr162Ter) | |
17 | g.41586349G>T | CA399481890 | KRT14 | c.486C>A (p.Tyr162Ter) | |
17 | g.41586350T>A | CA399481893 | KRT14 | c.485A>T (p.Tyr162Phe) | |
17 | g.41586350T>C | CA399481895 | KRT14 | c.485A>G (p.Tyr162Cys) | |
17 | g.41586350T>G | CA399481896 | KRT14 | c.485A>C (p.Tyr162Ser) | |
17 | g.41586351A= | CA2260086772 | KRT14 | c.484T= (p.Tyr162=) | |
17 | g.41586351A>C | CA399481904 | KRT14 | c.484T>G (p.Tyr162Asp) | |
17 | g.41586351A>G | CA399481900 | KRT14 | c.484T>C (p.Tyr162His) | gnomAD v4 |
17 | g.41586351A>T | CA399481902 | KRT14 | c.484T>A (p.Tyr162Asn) | dbSNP |
17 | g.41586351dup | CA2580093697 | KRT14 | c.484dup (p.Tyr162LeufsTer9) | ClinVar |
17 | g.41586352G>A | CA8562709 | KRT14 | c.483C>T (p.Asp161=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.41586352G>C | CA399481909 | KRT14 | c.483C>G (p.Asp161Glu) | |
17 | g.41586352G= | CA2260086773 | KRT14 | c.483C= (p.Asp161=) | |
17 | g.41586352G>T | CA399481910 | KRT14 | c.483C>A (p.Asp161Glu) | |
17 | g.41586353T>A | CA399481913 | KRT14 | c.482A>T (p.Asp161Val) |