Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
17 | g.41583773C>A | CA8562581 | KRT14 | c.914G>T (p.Trp305Leu) n.364G>T | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.41583773C= | CA2260085564 | KRT14 | c.914G= (p.Trp305=) n.364G= | |
17 | g.41583773C>G | CA399477079 | KRT14 | c.914G>C (p.Trp305Ser) n.364G>C | |
17 | g.41583773C>T | CA399477081 | KRT14 | c.914G>A (p.Trp305Ter) n.364G>A | gnomAD v4 |
17 | g.41583774A>C | CA399477084 | KRT14 | c.913T>G (p.Trp305Gly) n.363T>G | |
17 | g.41583774A>G | CA399477086 | KRT14 | c.913T>C (p.Trp305Arg) n.363T>C | |
17 | g.41583774A>T | CA399477088 | KRT14 | c.913T>A (p.Trp305Arg) n.363T>A | |
17 | g.41583775T>A | CA399477092 | KRT14 | c.912A>T (p.Glu304Asp) n.362A>T | |
17 | g.41583775T>C | CA500205437 | KRT14 | c.912A>G (p.Glu304=) n.362A>G | gnomAD v4 |
17 | g.41583775T>G | CA399477094 | KRT14 | c.912A>C (p.Glu304Asp) n.362A>C | |
17 | g.41583776T>A | CA399477097 | KRT14 | c.911A>T (p.Glu304Val) n.361A>T | |
17 | g.41583776T>C | CA399477100 | KRT14 | c.911A>G (p.Glu304Gly) n.361A>G | |
17 | g.41583776T>G | CA399477102 | KRT14 | c.911A>C (p.Glu304Ala) n.361A>C | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.41583776T= | CA2260085565 | KRT14 | c.911A= (p.Glu304=) n.361A= | |
17 | g.41583777C>A | CA399477105 | KRT14 | c.910G>T (p.Glu304Ter) n.360G>T | |
17 | g.41583777C>G | CA399477107 | KRT14 | c.910G>C (p.Glu304Gln) n.360G>C | |
17 | g.41583777C>T | CA399477106 | KRT14 | c.910G>A (p.Glu304Lys) n.360G>A | COSMIC |
17 | g.41583778C>A | CA399477111 | KRT14 | c.909G>T (p.Glu303Asp) n.359G>T | |
17 | g.41583778C>G | CA399477112 | KRT14 | c.909G>C (p.Glu303Asp) n.359G>C | |
17 | g.41583778C>T | CA500205440 | KRT14 | c.909G>A (p.Glu303=) n.359G>A | |
17 | g.41583779T>A | CA399477114 | KRT14 | c.908A>T (p.Glu303Val) n.358A>T | |
17 | g.41583779T>C | CA399477116 | KRT14 | c.908A>G (p.Glu303Gly) n.358A>G | |
17 | g.41583779T>G | CA399477117 | KRT14 | c.908A>C (p.Glu303Ala) n.358A>C | |
17 | g.41583780C>A | CA399477121 | KRT14 | c.907G>T (p.Glu303Ter) n.357G>T | |
17 | g.41583780C= | CA2260085566 | KRT14 | c.907G= (p.Glu303=) n.357G= | |
17 | g.41583780C>G | CA399477123 | KRT14 | c.907G>C (p.Glu303Gln) n.357G>C | |
17 | g.41583780C>T | CA399477125 | KRT14 | c.907G>A (p.Glu303Lys) n.357G>A | ClinVar dbSNP gnomAD v4 COSMIC |
17 | g.41583781G>A | CA8562582 | KRT14 | c.906C>T (p.Ala302=) n.356C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.41583781G>C | CA500205442 | KRT14 | c.906C>G (p.Ala302=) n.356C>G | |
17 | g.41583781G= | CA2260085567 | KRT14 | c.906C= (p.Ala302=) n.356C= | |
17 | g.41583781G>T | CA500205444 | KRT14 | c.906C>A (p.Ala302=) n.356C>A | gnomAD v4 |
17 | g.41583782G>A | CA399477127 | KRT14 | c.905C>T (p.Ala302Val) n.355C>T | |
17 | g.41583782G>C | CA399477128 | KRT14 | c.905C>G (p.Ala302Gly) n.355C>G | |
17 | g.41583782G>T | CA399477130 | KRT14 | c.905C>A (p.Ala302Asp) n.355C>A | |
17 | g.41583783C>A | CA399477133 | KRT14 | c.904G>T (p.Ala302Ser) n.354G>T | |
17 | g.41583783C>G | CA399477134 | KRT14 | c.904G>C (p.Ala302Pro) n.354G>C | |
17 | g.41583783C>T | CA399477136 | KRT14 | c.904G>A (p.Ala302Thr) n.354G>A | |
17 | g.41583784A>C | CA399477138 | KRT14 | c.903T>G (p.Asp301Glu) n.353T>G | |
17 | g.41583784A>G | CA500205452 | KRT14 | c.903T>C (p.Asp301=) n.353T>C | |
17 | g.41583784A>T | CA399477140 | KRT14 | c.903T>A (p.Asp301Glu) n.353T>A | |
17 | g.41583785T>A | CA399477144 | KRT14 | c.902A>T (p.Asp301Val) n.352A>T | |
17 | g.41583785T>C | CA399477146 | KRT14 | c.902A>G (p.Asp301Gly) n.352A>G | gnomAD v4 |
17 | g.41583785T>G | CA399477148 | KRT14 | c.902A>C (p.Asp301Ala) n.352A>C | |
17 | g.41583786C>A | CA399477151 | KRT14 | c.901G>T (p.Asp301Tyr) n.351G>T | |
17 | g.41583786C>G | CA399477152 | KRT14 | c.901G>C (p.Asp301His) n.351G>C | |
17 | g.41583786C>T | CA399477154 | KRT14 | c.901G>A (p.Asp301Asn) n.351G>A | |
17 | g.41583787C>A | CA399477157 | KRT14 | c.900G>T (p.Lys300Asn) n.350G>T | |
17 | g.41583787C= | CA2260085568 | KRT14 | c.900G= (p.Lys300=) n.350G= | |
17 | g.41583787C>G | CA399477159 | KRT14 | c.900G>C (p.Lys300Asn) n.350G>C | |
17 | g.41583787C>T | CA290665011 | KRT14 | c.900G>A (p.Lys300=) n.350G>A | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |