Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
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 | |
17 | g.41583793G>T | CA399477192 | KRT14 | c.894C>A (p.Asn298Lys) n.344C>A | |
17 | g.41583794T>A | CA399477196 | KRT14 | c.893A>T (p.Asn298Ile) n.343A>T | |
17 | g.41583794T>C | CA399477198 | KRT14 | c.893A>G (p.Asn298Ser) n.343A>G | |
17 | g.41583794T>G | CA399477200 | KRT14 | c.893A>C (p.Asn298Thr) n.343A>C | |
17 | g.41583795T>A | CA399477209 | KRT14 | c.892A>T (p.Asn298Tyr) n.342A>T | |
17 | g.41583795T>C | CA399477207 | KRT14 | c.892A>G (p.Asn298Asp) n.342A>G | |
17 | g.41583795T>G | CA399477204 | KRT14 | c.892A>C (p.Asn298His) n.342A>C | |
17 | g.41583796C>A | CA399477212 | KRT14 | c.891G>T (p.Lys297Asn) n.341G>T | |
17 | g.41583796C>G | CA399477215 | KRT14 | c.891G>C (p.Lys297Asn) n.341G>C | |
17 | g.41583796C>T | CA500205470 | KRT14 | c.891G>A (p.Lys297=) n.341G>A | |
17 | g.41583797T>A | CA399477216 | KRT14 | c.890A>T (p.Lys297Met) n.340A>T | |
17 | g.41583797T>C | CA399477217 | KRT14 | c.890A>G (p.Lys297Arg) n.340A>G | gnomAD v4 |
17 | g.41583797T>G | CA399477218 | KRT14 | c.890A>C (p.Lys297Thr) n.340A>C | |
17 | g.41583798T>A | CA399477221 | KRT14 | c.889A>T (p.Lys297Ter) n.339A>T | |
17 | g.41583798T>C | CA399477223 | KRT14 | c.889A>G (p.Lys297Glu) n.339A>G | |
17 | g.41583798T>G | CA399477225 | KRT14 | c.889A>C (p.Lys297Gln) n.339A>C | |
17 | g.41583799C>A | CA399477228 | KRT14 | c.888G>T (p.Glu296Asp) n.338G>T | COSMIC |
17 | g.41583799C= | CA2260085572 | KRT14 | c.888G= (p.Glu296=) n.338G= | |
17 | g.41583799C>G | CA399477230 | KRT14 | c.888G>C (p.Glu296Asp) n.338G>C | |
17 | g.41583799C>T | CA500205473 | KRT14 | c.888G>A (p.Glu296=) n.338G>A | dbSNP |