Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
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 |
17 | g.41583788T>A | CA399477164 | KRT14 | c.899A>T (p.Lys300Met) n.349A>T | |
17 | g.41583788T>C | CA399477165 | KRT14 | c.899A>G (p.Lys300Arg) n.349A>G | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.41583788T>G | CA399477166 | KRT14 | c.899A>C (p.Lys300Thr) n.349A>C | |
17 | g.41583788T= | CA2260085569 | KRT14 | c.899A= (p.Lys300=) n.349A= | |
17 | g.41583789T>A | CA399477169 | KRT14 | c.898A>T (p.Lys300Ter) n.348A>T | |
17 | g.41583789T>C | CA399477173 | KRT14 | c.898A>G (p.Lys300Glu) n.348A>G | |
17 | g.41583789T>G | CA399477170 | KRT14 | c.898A>C (p.Lys300Gln) n.348A>C | |
17 | g.41583790G>A | CA500205459 | KRT14 | c.897C>T (p.Arg299=) n.347C>T | |
17 | g.41583790G>C | CA500205461 | KRT14 | c.897C>G (p.Arg299=) n.347C>G | |
17 | g.41583790G>T | CA500205460 | KRT14 | c.897C>A (p.Arg299=) n.347C>A | |
17 | g.41583791C>A | CA399477176 | KRT14 | c.896G>T (p.Arg299Leu) n.346G>T | dbSNP gnomAD v3 gnomAD v4 |
17 | g.41583791C= | CA2260085570 | KRT14 | c.896G= (p.Arg299=) n.346G= | |
17 | g.41583791C>G | CA399477179 | KRT14 | c.896G>C (p.Arg299Pro) n.346G>C | |
17 | g.41583791C>T | CA8562583 | KRT14 | c.896G>A (p.Arg299His) n.346G>A | dbSNP ExAC gnomAD v2 gnomAD v4 |
17 | g.41583792G>A | CA399477184 | KRT14 | c.895C>T (p.Arg299Cys) n.345C>T | dbSNP gnomAD v4 |
17 | g.41583792G>C | CA399477186 | KRT14 | c.895C>G (p.Arg299Gly) n.345C>G | |
17 | g.41583792G= | CA2260085571 | KRT14 | c.895C= (p.Arg299=) n.345C= | |
17 | g.41583792G>T | CA399477189 | KRT14 | c.895C>A (p.Arg299Ser) n.345C>A | |
17 | g.41583793G>A | CA500205468 | KRT14 | c.894C>T (p.Asn298=) n.344C>T | gnomAD v4 |
17 | g.41583793G>C | CA399477191 | KRT14 | c.894C>G (p.Asn298Lys) n.344C>G |