| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 17 | g.41583337_41583366del | CA2695225880 | KRT14 | c.1151_1180del (p.Leu384_Gln393del) n.98_127del n.601_630del | |
| 17 | g.41583364_41583405dup | CA216817 | KRT14 | c.1117_1158dup (p.Gln386_Leu387insIleGlnGluMetIleGlySerValGluGluGlnLeuAlaGln) n.64_105dup n.567_608dup | ClinVar dbSNP |
| 17 | g.41583358A= | CA2260085369 | KRT14 | c.1151T= (p.Leu384=) n.98T= n.601T= | |
| 17 | g.41583358A>C | CA399475770 | KRT14 | c.1151T>G (p.Leu384Arg) n.98T>G n.601T>G | |
| 17 | g.41583358A>G | CA216827 | KRT14 | c.1151T>C (p.Leu384Pro) n.98T>C n.601T>C | ClinVar dbSNP |
| 17 | g.41583358A>T | CA399475771 | KRT14 | c.1151T>A (p.Leu384Gln) n.98T>A n.601T>A | |
| 17 | g.41583359G>A | CA500205599 | KRT14 | c.1150C>T (p.Leu384=) n.97C>T n.600C>T | |
| 17 | g.41583359G>C | CA399475772 | KRT14 | c.1150C>G (p.Leu384Val) n.97C>G n.600C>G | |
| 17 | g.41583359G>T | CA399475773 | KRT14 | c.1150C>A (p.Leu384Met) n.97C>A n.600C>A | |
| 17 | g.41583360C>A | CA399475774 | KRT14 | c.1149G>T (p.Gln383His) n.96G>T n.599G>T | gnomAD v4 |
| 17 | g.41583360C>G | CA399475775 | KRT14 | c.1149G>C (p.Gln383His) n.96G>C n.599G>C | |
| 17 | g.41583360C>T | CA500205603 | KRT14 | c.1149G>A (p.Gln383=) n.96G>A n.599G>A | |
| 17 | g.41583361T>A | CA399475776 | KRT14 | c.1148A>T (p.Gln383Leu) n.95A>T n.598A>T | |
| 17 | g.41583361T>C | CA399475777 | KRT14 | c.1148A>G (p.Gln383Arg) n.95A>G n.598A>G | |
| 17 | g.41583361T>G | CA399475778 | KRT14 | c.1148A>C (p.Gln383Pro) n.95A>C n.598A>C | dbSNP gnomAD v3 gnomAD v4 |
| 17 | g.41583361T= | CA2260085370 | KRT14 | c.1148A= (p.Gln383=) n.95A= n.598A= | |
| 17 | g.41583362G>A | CA399475779 | KRT14 | c.1147C>T (p.Gln383Ter) n.94C>T n.597C>T | |
| 17 | g.41583362G>C | CA399475780 | KRT14 | c.1147C>G (p.Gln383Glu) n.94C>G n.597C>G | |
| 17 | g.41583362G>T | CA399475781 | KRT14 | c.1147C>A (p.Gln383Lys) n.94C>A n.597C>A | gnomAD v4 |
| 17 | g.41583363C>A | CA399475782 | KRT14 | c.1146G>T (p.Glu382Asp) n.93G>T n.596G>T | |
| 17 | g.41583363C>G | CA399475783 | KRT14 | c.1146G>C (p.Glu382Asp) n.93G>C n.596G>C | |
| 17 | g.41583363C>T | CA500205609 | KRT14 | c.1146G>A (p.Glu382=) n.93G>A n.596G>A | gnomAD v4 COSMIC |
| 17 | g.41583364T>A | CA399475786 | KRT14 | c.1145A>T (p.Glu382Val) n.92A>T n.595A>T | |
| 17 | g.41583364T>C | CA399475784 | KRT14 | c.1145A>G (p.Glu382Gly) n.92A>G n.595A>G | |
| 17 | g.41583364T>G | CA399475785 | KRT14 | c.1145A>C (p.Glu382Ala) n.92A>C n.595A>C | |
| 17 | g.41583365C>A | CA399475787 | KRT14 | c.1144G>T (p.Glu382Ter) n.91G>T n.594G>T | ClinVar dbSNP |
| 17 | g.41583365C= | CA2260085371 | KRT14 | c.1144G= (p.Glu382=) n.91G= n.594G= | |
| 17 | g.41583365C>G | CA399475788 | KRT14 | c.1144G>C (p.Glu382Gln) n.91G>C n.594G>C | |
| 17 | g.41583365C>T | CA8562487 | KRT14 | c.1144G>A (p.Glu382Lys) n.91G>A n.594G>A | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 17 | g.41583366C>A | CA399475789 | KRT14 | c.1143G>T (p.Glu381Asp) n.90G>T n.593G>T | |
| 17 | g.41583366C>G | CA399475790 | KRT14 | c.1143G>C (p.Glu381Asp) n.90G>C n.593G>C | |
| 17 | g.41583366C>T | CA500205611 | KRT14 | c.1143G>A (p.Glu381=) n.90G>A n.593G>A | |
| 17 | g.41583367T>A | CA399475791 | KRT14 | c.1142A>T (p.Glu381Val) n.89A>T n.592A>T | |
| 17 | g.41583367T>C | CA399475792 | KRT14 | c.1142A>G (p.Glu381Gly) n.89A>G n.592A>G | |
| 17 | g.41583367T>G | CA399475793 | KRT14 | c.1142A>C (p.Glu381Ala) n.89A>C n.592A>C | |
| 17 | g.41583368C>A | CA399475794 | KRT14 | c.1141G>T (p.Glu381Ter) n.88G>T n.591G>T | |
| 17 | g.41583368C= | CA2260085372 | KRT14 | c.1141G= (p.Glu381=) n.88G= n.591G= | |
| 17 | g.41583368C>G | CA399475795 | KRT14 | c.1141G>C (p.Glu381Gln) n.88G>C n.591G>C | dbSNP |
| 17 | g.41583368C>T | CA216825 | KRT14 | c.1141G>A (p.Glu381Lys) n.88G>A n.591G>A | ClinVar dbSNP COSMIC |
| 17 | g.41583369del | CA2637834504 | KRT14 | c.1141del (p.Glu381ArgfsTer24) n.88del n.591del | gnomAD v4 |
| 17 | g.41583369C>A | CA500205619 | KRT14 | c.1140G>T (p.Val380=) n.87G>T n.590G>T | |
| 17 | g.41583369C= | CA2260085373 | KRT14 | c.1140G= (p.Val380=) n.87G= n.590G= | |
| 17 | g.41583369C>G | CA8562488 | KRT14 | c.1140G>C (p.Val380=) n.87G>C n.590G>C | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 17 | g.41583369C>T | CA500205618 | KRT14 | c.1140G>A (p.Val380=) n.87G>A n.590G>A | |
| 17 | g.41583370A>C | CA399475798 | KRT14 | c.1139T>G (p.Val380Gly) n.86T>G n.589T>G | |
| 17 | g.41583370A>G | CA399475796 | KRT14 | c.1139T>C (p.Val380Ala) n.86T>C n.589T>C | |
| 17 | g.41583370A>T | CA399475797 | KRT14 | c.1139T>A (p.Val380Glu) n.86T>A n.589T>A | |
| 17 | g.41583371C>A | CA399475799 | KRT14 | c.1138G>T (p.Val380Leu) n.85G>T n.588G>T | dbSNP |
| 17 | g.41583371C= | CA2260085374 | KRT14 | c.1138G= (p.Val380=) n.85G= n.588G= | |
| 17 | g.41583371C>G | CA399475800 | KRT14 | c.1138G>C (p.Val380Leu) n.85G>C n.588G>C | gnomAD v4 |