Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
17 | g.41586365_41586367delinsCTG | CA2739267535 | KRT14 | c.468_470delinsCAG (p.Ala157Ser) | |
17 | g.41586365_41586367delinsGCA | CA2260086777 | KRT14 | c.468_470delinsTGC (p.Pro156=) | |
17 | g.41586366_41586367del | CA8562712 | KRT14 | c.468_469del (p.Ala157Ter) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.41586367A= | CA2260086780 | KRT14 | c.468T= (p.Pro156=) | |
17 | g.41586367A>C | CA499991836 | KRT14 | c.468T>G (p.Pro156=) | |
17 | g.41586367A>G | CA499991837 | KRT14 | c.468T>C (p.Pro156=) | dbSNP |
17 | g.41586367A>T | CA499991838 | KRT14 | c.468T>A (p.Pro156=) | |
17 | g.41586368G>A | CA399481987 | KRT14 | c.467C>T (p.Pro156Leu) | gnomAD v4 |
17 | g.41586368G>C | CA399481988 | KRT14 | c.467C>G (p.Pro156Arg) | |
17 | g.41586368G>T | CA399481991 | KRT14 | c.467C>A (p.Pro156His) | gnomAD v4 |
17 | g.41586369G>A | CA399482002 | KRT14 | c.466C>T (p.Pro156Ser) | gnomAD v4 |
17 | g.41586369G>C | CA399482000 | KRT14 | c.466C>G (p.Pro156Ala) | |
17 | g.41586369G= | CA2260086781 | KRT14 | c.466C= (p.Pro156=) | |
17 | g.41586369G>T | CA399481994 | KRT14 | c.466C>A (p.Pro156Thr) | dbSNP gnomAD v3 gnomAD v4 |
17 | g.41586370C>A | CA499991840 | KRT14 | c.465G>T (p.Arg155=) | |
17 | g.41586370C>G | CA499991841 | KRT14 | c.465G>C (p.Arg155=) | |
17 | g.41586370C>T | CA499991842 | KRT14 | c.465G>A (p.Arg155=) | |
17 | g.41586371C>A | CA399482012 | KRT14 | c.464G>T (p.Arg155Leu) | |
17 | g.41586371C= | CA2260086782 | KRT14 | c.464G= (p.Arg155=) | |
17 | g.41586371C>G | CA399482005 | KRT14 | c.464G>C (p.Arg155Pro) | dbSNP gnomAD v4 |
17 | g.41586371C>T | CA8562714 | KRT14 | c.464G>A (p.Arg155Gln) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
17 | g.41586372G>A | CA8562715 | KRT14 | c.463C>T (p.Arg155Trp) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.41586372G>C | CA399482016 | KRT14 | c.463C>G (p.Arg155Gly) | |
17 | g.41586372G= | CA2260086783 | KRT14 | c.463C= (p.Arg155=) | |
17 | g.41586372G>T | CA499991846 | KRT14 | c.463C>A (p.Arg155=) | gnomAD v4 |
17 | g.41586373C>A | CA399482018 | KRT14 | c.462G>T (p.Gln154His) | |
17 | g.41586373C>G | CA399482020 | KRT14 | c.462G>C (p.Gln154His) | |
17 | g.41586373C>T | CA499991848 | KRT14 | c.462G>A (p.Gln154=) | |
17 | g.41586374T>A | CA399482026 | KRT14 | c.461A>T (p.Gln154Leu) | |
17 | g.41586374T>C | CA399482022 | KRT14 | c.461A>G (p.Gln154Arg) | |
17 | g.41586374T>G | CA399482025 | KRT14 | c.461A>C (p.Gln154Pro) | |
17 | g.41586375G>A | CA399482028 | KRT14 | c.460C>T (p.Gln154Ter) | |
17 | g.41586375G>C | CA399482031 | KRT14 | c.460C>G (p.Gln154Glu) | dbSNP gnomAD v4 |
17 | g.41586375G>T | CA399482034 | KRT14 | c.460C>A (p.Gln154Lys) | |
17 | g.41586376C>A | CA399482036 | KRT14 | c.459G>T (p.Arg153Ser) | |
17 | g.41586376C>G | CA399482039 | KRT14 | c.459G>C (p.Arg153Ser) | |
17 | g.41586376C>T | CA499991854 | KRT14 | c.459G>A (p.Arg153=) | |
17 | g.41586377C>A | CA399482042 | KRT14 | c.458G>T (p.Arg153Met) | |
17 | g.41586377C>G | CA399482047 | KRT14 | c.458G>C (p.Arg153Thr) | |
17 | g.41586377C>T | CA399482045 | KRT14 | c.458G>A (p.Arg153Lys) | |
17 | g.41586378T>A | CA399482048 | KRT14 | c.457A>T (p.Arg153Trp) | |
17 | g.41586378T>C | CA399482049 | KRT14 | c.457A>G (p.Arg153Gly) | |
17 | g.41586378T>G | CA499991858 | KRT14 | c.457A>C (p.Arg153=) | |
17 | g.41586379C>A | CA399482051 | KRT14 | c.456G>T (p.Gln152His) | |
17 | g.41586379C= | CA2260086784 | KRT14 | c.456G= (p.Gln152=) | |
17 | g.41586379C>G | CA8562716 | KRT14 | c.456G>C (p.Gln152His) | dbSNP ExAC gnomAD v2 gnomAD v4 |
17 | g.41586379C>T | CA499991860 | KRT14 | c.456G>A (p.Gln152=) | |
17 | g.41586380T>A | CA399482054 | KRT14 | c.455A>T (p.Gln152Leu) | |
17 | g.41586380T>C | CA399482055 | KRT14 | c.455A>G (p.Gln152Arg) | |
17 | g.41586380T>G | CA399482057 | KRT14 | c.455A>C (p.Gln152Pro) |