Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
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) | |
17 | g.41586381G>A | CA399482059 | KRT14 | c.454C>T (p.Gln152Ter) | gnomAD v4 |
17 | g.41586381G>C | CA399482061 | KRT14 | c.454C>G (p.Gln152Glu) | |
17 | g.41586381G>T | CA399482063 | KRT14 | c.454C>A (p.Gln152Lys) | |
17 | g.41586382G>A | CA499991864 | KRT14 | c.453C>T (p.Tyr151=) | |
17 | g.41586382G>C | CA399482065 | KRT14 | c.453C>G (p.Tyr151Ter) | |
17 | g.41586382G>T | CA399482067 | KRT14 | c.453C>A (p.Tyr151Ter) | |
17 | g.41586383T>A | CA399482071 | KRT14 | c.452A>T (p.Tyr151Phe) | |
17 | g.41586383T>C | CA399482073 | KRT14 | c.452A>G (p.Tyr151Cys) | dbSNP |
17 | g.41586383T>G | CA399482069 | KRT14 | c.452A>C (p.Tyr151Ser) | |
17 | g.41586383T= | CA2260086785 | KRT14 | c.452A= (p.Tyr151=) | |
17 | g.41586384A>C | CA399482075 | KRT14 | c.451T>G (p.Tyr151Asp) | |
17 | g.41586384A>G | CA399482077 | KRT14 | c.451T>C (p.Tyr151His) | |
17 | g.41586384A>T | CA399482079 | KRT14 | c.451T>A (p.Tyr151Asn) | |
17 | g.41586385C>A | CA399482081 | KRT14 | c.450G>T (p.Trp150Cys) | |
17 | g.41586385C>G | CA399482083 | KRT14 | c.450G>C (p.Trp150Cys) | |
17 | g.41586385C>T | CA399482085 | KRT14 | c.450G>A (p.Trp150Ter) | |
17 | g.41586386C>A | CA399482091 | KRT14 | c.449G>T (p.Trp150Leu) | |
17 | g.41586386C>G | CA399482087 | KRT14 | c.449G>C (p.Trp150Ser) | |
17 | g.41586386C>T | CA399482089 | KRT14 | c.449G>A (p.Trp150Ter) | gnomAD v4 |
17 | g.41586386_41586387del | CA2637837248 | KRT14 | c.448_449del (p.Trp150ValfsTer8) | gnomAD v4 |
17 | g.41586387A>C | CA399482093 | KRT14 | c.448T>G (p.Trp150Gly) | gnomAD v4 |
17 | g.41586387A>G | CA399482095 | KRT14 | c.448T>C (p.Trp150Arg) | |
17 | g.41586387A>T | CA399482097 | KRT14 | c.448T>A (p.Trp150Arg) | |
17 | g.41586388G>A | CA499991874 | KRT14 | c.447C>T (p.Asp149=) | |
17 | g.41586388G>C | CA399482098 | KRT14 | c.447C>G (p.Asp149Glu) | |
17 | g.41586388G>T | CA399482100 | KRT14 | c.447C>A (p.Asp149Glu) | |
17 | g.41586389T>A | CA399482104 | KRT14 | c.446A>T (p.Asp149Val) | |
17 | g.41586389T>C | CA8562717 | KRT14 | c.446A>G (p.Asp149Gly) | dbSNP ExAC gnomAD v2 gnomAD v4 |