Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
17 | g.41583867C>A | CA399477554 | KRT14 | c.820G>T (p.Ala274Ser) n.270G>T | |
17 | g.41583867C= | CA2260085597 | KRT14 | c.820G= (p.Ala274=) n.270G= | |
17 | g.41583867C>G | CA399477556 | KRT14 | c.820G>C (p.Ala274Pro) n.270G>C | |
17 | g.41583867C>T | CA8562600 | KRT14 | c.820G>A (p.Ala274Thr) n.270G>A | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.41583868G>A | CA8562601 | KRT14 | c.819C>T (p.Asp273=) n.269C>T | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.41583868G>C | CA399477565 | KRT14 | c.819C>G (p.Asp273Glu) n.269C>G | dbSNP gnomAD v4 |
17 | g.41583868G= | CA2260085598 | KRT14 | c.819C= (p.Asp273=) n.269C= | |
17 | g.41583868G>T | CA399477567 | KRT14 | c.819C>A (p.Asp273Glu) n.269C>A | |
17 | g.41583869T>A | CA399477570 | KRT14 | c.818A>T (p.Asp273Val) n.268A>T | |
17 | g.41583869T>C | CA216984 | KRT14 | c.818A>G (p.Asp273Gly) n.268A>G | ClinVar dbSNP |
17 | g.41583869T>G | CA399477572 | KRT14 | c.818A>C (p.Asp273Ala) n.268A>C | |
17 | g.41583869T= | CA2260085599 | KRT14 | c.818A= (p.Asp273=) n.268A= | |
17 | g.41583870C>A | CA399477576 | KRT14 | c.817G>T (p.Asp273Tyr) n.267G>T | |
17 | g.41583870C= | CA2260085600 | KRT14 | c.817G= (p.Asp273=) n.267G= | |
17 | g.41583870C>G | CA399477577 | KRT14 | c.817G>C (p.Asp273His) n.267G>C | gnomAD v4 |
17 | g.41583870C>T | CA399477578 | KRT14 | c.817G>A (p.Asp273Asn) n.267G>A | dbSNP gnomAD v4 COSMIC |
17 | g.41583871C>A | CA399477582 | KRT14 | c.816G>T (p.Met272Ile) n.266G>T | |
17 | g.41583871C>G | CA399477584 | KRT14 | c.816G>C (p.Met272Ile) n.266G>C | |
17 | g.41583871C>T | CA399477586 | KRT14 | c.816G>A (p.Met272Ile) n.266G>A | |
17 | g.41583880_41583893del | CA2637835339 | KRT14 | c.803_816del (p.Val268GlyfsTer17) n.253_266del | gnomAD v4 |
17 | g.41583872A= | CA2260085601 | KRT14 | c.815T= (p.Met272=) n.265T= | |
17 | g.41583872A>C | CA216982 | KRT14 | c.815T>G (p.Met272Arg) n.265T>G | ClinVar dbSNP |
17 | g.41583872A>G | CA216980 | KRT14 | c.815T>C (p.Met272Thr) n.265T>C | ClinVar dbSNP |
17 | g.41583872A>T | CA399477592 | KRT14 | c.815T>A (p.Met272Lys) n.265T>A | ClinVar |
17 | g.41583873T>A | CA399477596 | KRT14 | c.814A>T (p.Met272Leu) n.264A>T | |
17 | g.41583873T>C | CA399477598 | KRT14 | c.814A>G (p.Met272Val) n.264A>G | |
17 | g.41583873T>G | CA399477600 | KRT14 | c.814A>C (p.Met272Leu) n.264A>C | |
17 | g.41583874C>A | CA399477605 | KRT14 | c.813G>T (p.Glu271Asp) n.263G>T | |
17 | g.41583874C>G | CA399477603 | KRT14 | c.813G>C (p.Glu271Asp) n.263G>C | |
17 | g.41583874C>T | CA500205655 | KRT14 | c.813G>A (p.Glu271=) n.263G>A | |
17 | g.41583875T>A | CA399477608 | KRT14 | c.812A>T (p.Glu271Val) n.262A>T | |
17 | g.41583875T>C | CA399477610 | KRT14 | c.812A>G (p.Glu271Gly) n.262A>G | |
17 | g.41583875T>G | CA399477612 | KRT14 | c.812A>C (p.Glu271Ala) n.262A>C | |
17 | g.41583876C>A | CA399477615 | KRT14 | c.811G>T (p.Glu271Ter) n.261G>T | |
17 | g.41583876C>G | CA399477618 | KRT14 | c.811G>C (p.Glu271Gln) n.261G>C | |
17 | g.41583876C>T | CA399477619 | KRT14 | c.811G>A (p.Glu271Lys) n.261G>A | |
17 | g.41583877C>A | CA500205662 | KRT14 | c.810G>T (p.Val270=) n.260G>T | |
17 | g.41583877C>G | CA500205664 | KRT14 | c.810G>C (p.Val270=) n.260G>C | |
17 | g.41583877C>T | CA500205665 | KRT14 | c.810G>A (p.Val270=) n.260G>A | |
17 | g.41583878A>C | CA399477623 | KRT14 | c.809T>G (p.Val270Gly) n.259T>G | |
17 | g.41583878A>G | CA399477625 | KRT14 | c.809T>C (p.Val270Ala) n.259T>C | |
17 | g.41583878A>T | CA399477627 | KRT14 | c.809T>A (p.Val270Glu) n.259T>A | |
17 | g.41583879C>A | CA399477629 | KRT14 | c.808G>T (p.Val270Leu) n.258G>T | |
17 | g.41583879C= | CA2260085602 | KRT14 | c.808G= (p.Val270=) n.258G= | |
17 | g.41583879C>G | CA399477631 | KRT14 | c.808G>C (p.Val270Leu) n.258G>C | |
17 | g.41583879C>T | CA216978 | KRT14 | c.808G>A (p.Val270Met) n.258G>A | ClinVar dbSNP |
17 | g.41583880A= | CA2260085603 | KRT14 | c.807T= (p.Asn269=) n.257T= | |
17 | g.41583880A>C | CA399477635 | KRT14 | c.807T>G (p.Asn269Lys) n.257T>G | |
17 | g.41583880A>G | CA8562602 | KRT14 | c.807T>C (p.Asn269=) n.257T>C | dbSNP ExAC gnomAD v2 |
17 | g.41583880A>T | CA399477634 | KRT14 | c.807T>A (p.Asn269Lys) n.257T>A | |
17 | g.41583881T>A | CA399477636 | KRT14 | c.806A>T (p.Asn269Ile) n.256A>T | |
17 | g.41583881T>C | CA399477637 | KRT14 | c.806A>G (p.Asn269Ser) n.256A>G | dbSNP gnomAD v3 gnomAD v4 |
17 | g.41583881T>G | CA399477638 | KRT14 | c.806A>C (p.Asn269Thr) n.256A>C | |
17 | g.41583881T= | CA2260085604 | KRT14 | c.806A= (p.Asn269=) n.256A= | |
17 | g.41583882T>A | CA399477639 | KRT14 | c.805A>T (p.Asn269Tyr) n.255A>T | |
17 | g.41583882T>C | CA399477640 | KRT14 | c.805A>G (p.Asn269Asp) n.255A>G | |
17 | g.41583882T>G | CA399477641 | KRT14 | c.805A>C (p.Asn269His) n.255A>C | |
17 | g.41583883G>A | CA500205678 | KRT14 | c.804C>T (p.Val268=) n.254C>T | |
17 | g.41583883G>C | CA500205680 | KRT14 | c.804C>G (p.Val268=) n.254C>G | |
17 | g.41583883G>T | CA500205679 | KRT14 | c.804C>A (p.Val268=) n.254C>A | COSMIC |
17 | g.41583884A= | CA2260085605 | KRT14 | c.803T= (p.Val268=) n.253T= | |
17 | g.41583884A>C | CA399477643 | KRT14 | c.803T>G (p.Val268Gly) n.253T>G | |
17 | g.41583884A>G | CA399477642 | KRT14 | c.803T>C (p.Val268Ala) n.253T>C | ClinVar |
17 | g.41583884A>T | CA216976 | KRT14 | c.803T>A (p.Val268Asp) n.253T>A | ClinVar dbSNP |
17 | g.41583885C>A | CA399477644 | KRT14 | c.802G>T (p.Val268Phe) n.252G>T | |
17 | g.41583885C= | CA2260085606 | KRT14 | c.802G= (p.Val268=) n.252G= | |
17 | g.41583885C>G | CA399477645 | KRT14 | c.802G>C (p.Val268Leu) n.252G>C | |
17 | g.41583885C>T | CA399477646 | KRT14 | c.802G>A (p.Val268Ile) n.252G>A | dbSNP |
17 | g.41583886A= | CA2260085607 | KRT14 | c.801T= (p.Asp267=) n.251T= | |
17 | g.41583886A>C | CA399477647 | KRT14 | c.801T>G (p.Asp267Glu) n.251T>G | |
17 | g.41583886A>G | CA8562603 | KRT14 | c.801T>C (p.Asp267=) n.251T>C | dbSNP ExAC gnomAD v2 gnomAD v4 |
17 | g.41583886A>T | CA399477648 | KRT14 | c.801T>A (p.Asp267Glu) n.251T>A | |
17 | g.41583887T>A | CA399477649 | KRT14 | c.800A>T (p.Asp267Val) n.250A>T | |
17 | g.41583887T>C | CA399477651 | KRT14 | c.800A>G (p.Asp267Gly) n.250A>G | |
17 | g.41583887T>G | CA399477650 | KRT14 | c.800A>C (p.Asp267Ala) n.250A>C | |
17 | g.41583888C>A | CA399477652 | KRT14 | c.799G>T (p.Asp267Tyr) n.249G>T | |
17 | g.41583888C= | CA2260085608 | KRT14 | c.799G= (p.Asp267=) n.249G= | |
17 | g.41583888C>G | CA399477653 | KRT14 | c.799G>C (p.Asp267His) n.249G>C | gnomAD v4 |
17 | g.41583888C>T | CA290665037 | KRT14 | c.799G>A (p.Asp267Asn) n.249G>A | dbSNP |
17 | g.41583889T>A | CA500205696 | KRT14 | c.798A>T (p.Gly266=) n.248A>T | |
17 | g.41583889T>C | CA500205697 | KRT14 | c.798A>G (p.Gly266=) n.248A>G | |
17 | g.41583889T>G | CA500205701 | KRT14 | c.798A>C (p.Gly266=) n.248A>C | |
17 | g.41583890C>A | CA399477654 | KRT14 | c.797G>T (p.Gly266Val) n.247G>T | gnomAD v4 |
17 | g.41583890C>G | CA399477655 | KRT14 | c.797G>C (p.Gly266Ala) n.247G>C | |
17 | g.41583890C>T | CA399477656 | KRT14 | c.797G>A (p.Gly266Glu) n.247G>A | |
17 | g.41583891C>A | CA399477657 | KRT14 | c.796G>T (p.Gly266Ter) n.246G>T | |
17 | g.41583891C>G | CA399477658 | KRT14 | c.796G>C (p.Gly266Arg) n.246G>C | |
17 | g.41583891C>T | CA399477659 | KRT14 | c.796G>A (p.Gly266Arg) n.246G>A | gnomAD v4 COSMIC |
17 | g.41583892A>C | CA500205705 | KRT14 | c.795T>G (p.Gly265=) n.245T>G | |
17 | g.41583892A>G | CA500205706 | KRT14 | c.795T>C (p.Gly265=) n.245T>C | |
17 | g.41583892A>T | CA500205707 | KRT14 | c.795T>A (p.Gly265=) n.245T>A | |
17 | g.41583893C>A | CA399477660 | KRT14 | c.794G>T (p.Gly265Val) n.244G>T | |
17 | g.41583893C>G | CA399477661 | KRT14 | c.794G>C (p.Gly265Ala) n.244G>C | |
17 | g.41583893C>T | CA399477662 | KRT14 | c.794G>A (p.Gly265Asp) n.244G>A | |
17 | g.41583894C>A | CA399477663 | KRT14 | c.793G>T (p.Gly265Cys) n.243G>T | |
17 | g.41583894C= | CA2260085609 | KRT14 | c.793G= (p.Gly265=) n.243G= | |
17 | g.41583894C>G | CA399477665 | KRT14 | c.793G>C (p.Gly265Arg) n.243G>C | dbSNP gnomAD v2 gnomAD v4 |
17 | g.41583894C>T | CA399477664 | KRT14 | c.793G>A (p.Gly265Ser) n.243G>A | gnomAD v4 |
17 | g.41583895C>A | CA500205715 | KRT14 | c.792G>T (p.Val264=) n.242G>T | |
17 | g.41583895C= | CA2260085610 | KRT14 | c.792G= (p.Val264=) n.242G= | |
17 | g.41583895C>G | CA500205716 | KRT14 | c.792G>C (p.Val264=) n.242G>C | |
17 | g.41583895C>T | CA8562604 | KRT14 | c.792G>A (p.Val264=) n.242G>A | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.41583896A>C | CA399477666 | KRT14 | c.791T>G (p.Val264Gly) n.241T>G | gnomAD v4 |
17 | g.41583896A>G | CA399477667 | KRT14 | c.791T>C (p.Val264Ala) n.241T>C | |
17 | g.41583896A>T | CA399477668 | KRT14 | c.791T>A (p.Val264Glu) n.241T>A | |
17 | g.41583897C>A | CA399477669 | KRT14 | c.790G>T (p.Val264Leu) n.240G>T | |
17 | g.41583897C= | CA2260085611 | KRT14 | c.790G= (p.Val264=) n.240G= | |
17 | g.41583897C>G | CA399477670 | KRT14 | c.790G>C (p.Val264Leu) n.240G>C | |
17 | g.41583897C>T | CA8562605 | KRT14 | c.790G>A (p.Val264Met) n.240G>A | dbSNP ExAC gnomAD v2 gnomAD v4 |
17 | g.41583898C>A | CA399477671 | KRT14 | c.789G>T (p.Gln263His) n.239G>T | COSMIC |
17 | g.41583898C>G | CA399477672 | KRT14 | c.789G>C (p.Gln263His) n.239G>C | |
17 | g.41583898C>T | CA500205719 | KRT14 | c.789G>A (p.Gln263=) n.239G>A | |
17 | g.41583899T>A | CA399477673 | KRT14 | c.788A>T (p.Gln263Leu) n.238A>T | |
17 | g.41583899T>C | CA399477674 | KRT14 | c.788A>G (p.Gln263Arg) n.238A>G | dbSNP gnomAD v4 |
17 | g.41583899T>G | CA399477675 | KRT14 | c.788A>C (p.Gln263Pro) n.238A>C | |
17 | g.41583899T= | CA2260085612 | KRT14 | c.788A= (p.Gln263=) n.238A= | |
17 | g.41583900G>A | CA399477678 | KRT14 | c.787C>T (p.Gln263Ter) n.237C>T | gnomAD v4 |
17 | g.41583900G>C | CA399477676 | KRT14 | c.787C>G (p.Gln263Glu) n.237C>G | |
17 | g.41583900G>T | CA399477677 | KRT14 | c.787C>A (p.Gln263Lys) n.237C>A | |
17 | g.41583901G>A | CA8562606 | KRT14 | c.786C>T (p.Gly262=) n.236C>T | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.41583901G>C | CA500205724 | KRT14 | c.786C>G (p.Gly262=) n.236C>G | |
17 | g.41583901G= | CA2260085613 | KRT14 | c.786C= (p.Gly262=) n.236C= | |
17 | g.41583901G>T | CA500205725 | KRT14 | c.786C>A (p.Gly262=) n.236C>A | |
17 | g.41583902C>A | CA399477679 | KRT14 | c.785G>T (p.Gly262Val) n.235G>T | |
17 | g.41583902C>G | CA399477680 | KRT14 | c.785G>C (p.Gly262Ala) n.235G>C | |
17 | g.41583902C>T | CA399477681 | KRT14 | c.785G>A (p.Gly262Asp) n.235G>A | |
17 | g.41583903C>A | CA399477682 | KRT14 | c.784G>T (p.Gly262Cys) n.234G>T | |
17 | g.41583903C= | CA2260085614 | KRT14 | c.784G= (p.Gly262=) n.234G= | |
17 | g.41583903C>G | CA399477683 | KRT14 | c.784G>C (p.Gly262Arg) n.234G>C | |
17 | g.41583903C>T | CA8562607 | KRT14 | c.784G>A (p.Gly262Ser) n.234G>A | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.41583904T>A | CA399477684 | KRT14 | c.783A>T (p.Arg261Ser) n.233A>T | |
17 | g.41583904T>C | CA500205728 | KRT14 | c.783A>G (p.Arg261=) n.233A>G | dbSNP |
17 | g.41583904T>G | CA399477685 | KRT14 | c.783A>C (p.Arg261Ser) n.233A>C | |
17 | g.41583904T= | CA2260085615 | KRT14 | c.783A= (p.Arg261=) n.233A= | |
17 | g.41583905C>A | CA399477686 | KRT14 | c.782G>T (p.Arg261Ile) n.232G>T | |
17 | g.41583905C= | CA2260085616 | KRT14 | c.782G= (p.Arg261=) n.232G= | |
17 | g.41583905C>G | CA399477687 | KRT14 | c.782G>C (p.Arg261Thr) n.232G>C | dbSNP |
17 | g.41583905C>T | CA399477688 | KRT14 | c.782G>A (p.Arg261Lys) n.232G>A | |
17 | g.41583906T>A | CA399477689 | KRT14 | c.781A>T (p.Arg261Ter) n.231A>T | |
17 | g.41583906T>C | CA399477690 | KRT14 | c.781A>G (p.Arg261Gly) n.231A>G | |
17 | g.41583906T>G | CA500205730 | KRT14 | c.781A>C (p.Arg261=) n.231A>C | |
17 | g.41583907C>A | CA500205731 | KRT14 | c.780G>T (p.Leu260=) n.230G>T | |
17 | g.41583907C>G | CA500205733 | KRT14 | c.780G>C (p.Leu260=) n.230G>C | gnomAD v4 COSMIC |
17 | g.41583907C>T | CA500205732 | KRT14 | c.780G>A (p.Leu260=) n.230G>A | |
17 | g.41583908A= | CA2260085617 | KRT14 | c.779T= (p.Leu260=) n.229T= | |
17 | g.41583908A>C | CA399477691 | KRT14 | c.779T>G (p.Leu260Arg) n.229T>G | |
17 | g.41583908A>G | CA399477693 | KRT14 | c.779T>C (p.Leu260Pro) n.229T>C | dbSNP gnomAD v2 gnomAD v4 |
17 | g.41583908A>T | CA399477692 | KRT14 | c.779T>A (p.Leu260Gln) n.229T>A | |
17 | g.41583909G>A | CA500205737 | KRT14 | c.778C>T (p.Leu260=) n.228C>T | gnomAD v4 |
17 | g.41583909G>C | CA399477694 | KRT14 | c.778C>G (p.Leu260Val) n.228C>G | |
17 | g.41583909G= | CA2260085618 | KRT14 | c.778C= (p.Leu260=) n.228C= | |
17 | g.41583909G>T | CA399477695 | KRT14 | c.778C>A (p.Leu260Met) n.228C>A | dbSNP gnomAD v2 gnomAD v4 |
17 | g.41583910G>A | CA500205743 | KRT14 | c.777C>T (p.Ala259=) n.227C>T | |
17 | g.41583910G>C | CA500205739 | KRT14 | c.777C>G (p.Ala259=) n.227C>G | |
17 | g.41583910G>T | CA500205741 | KRT14 | c.777C>A (p.Ala259=) n.227C>A | |
17 | g.41583911G>A | CA399477696 | KRT14 | c.776C>T (p.Ala259Val) n.226C>T | dbSNP |
17 | g.41583911G>C | CA399477698 | KRT14 | c.776C>G (p.Ala259Gly) n.226C>G | |
17 | g.41583911G= | CA2260085619 | KRT14 | c.776C= (p.Ala259=) n.226C= | |
17 | g.41583911G>T | CA399477697 | KRT14 | c.776C>A (p.Ala259Asp) n.226C>A | |
17 | g.41583912C>A | CA399477699 | KRT14 | c.775G>T (p.Ala259Ser) n.225G>T | |
17 | g.41583912C>G | CA399477700 | KRT14 | c.775G>C (p.Ala259Pro) n.225G>C | gnomAD v4 |
17 | g.41583912C>T | CA399477701 | KRT14 | c.775G>A (p.Ala259Thr) n.225G>A | COSMIC |
17 | g.41583913A>C | CA399477702 | KRT14 | c.774T>G (p.Asn258Lys) n.224T>G | |
17 | g.41583913A>G | CA500205747 | KRT14 | c.774T>C (p.Asn258=) n.224T>C | |
17 | g.41583913A>T | CA399477703 | KRT14 | c.774T>A (p.Asn258Lys) n.224T>A | gnomAD v4 |
17 | g.41583914T>A | CA399477704 | KRT14 | c.773A>T (p.Asn258Ile) n.223A>T | gnomAD v4 |
17 | g.41583914T>C | CA399477705 | KRT14 | c.773A>G (p.Asn258Ser) n.223A>G | |
17 | g.41583914T>G | CA399477706 | KRT14 | c.773A>C (p.Asn258Thr) n.223A>C | |
17 | g.41583915T>A | CA399477707 | KRT14 | c.772A>T (p.Asn258Tyr) n.222A>T | |
17 | g.41583915T>C | CA399477708 | KRT14 | c.772A>G (p.Asn258Asp) n.222A>G | |
17 | g.41583915T>G | CA399477709 | KRT14 | c.772A>C (p.Asn258His) n.222A>C | |
17 | g.41583916C>A | CA399477711 | KRT14 | c.771G>T (p.Met257Ile) n.221G>T | |
17 | g.41583916C= | CA2260085620 | KRT14 | c.771G= (p.Met257=) n.221G= | |
17 | g.41583916C>G | CA399477710 | KRT14 | c.771G>C (p.Met257Ile) n.221G>C | |
17 | g.41583916C>T | CA290665046 | KRT14 | c.771G>A (p.Met257Ile) n.221G>A | dbSNP |
17 | g.41583917A= | CA2260085621 | KRT14 | c.770T= (p.Met257=) n.220T= | |
17 | g.41583917A>C | CA399477712 | KRT14 | c.770T>G (p.Met257Arg) n.220T>G | dbSNP gnomAD v3 gnomAD v4 |
17 | g.41583917A>G | CA8562608 | KRT14 | c.770T>C (p.Met257Thr) n.220T>C | dbSNP ExAC gnomAD v2 gnomAD v4 |
17 | g.41583917A>T | CA399477713 | KRT14 | c.770T>A (p.Met257Lys) n.220T>A | dbSNP |
17 | g.41583918T>A | CA399477714 | KRT14 | c.769A>T (p.Met257Leu) n.219A>T | |
17 | g.41583918T>C | CA399477715 | KRT14 | c.769A>G (p.Met257Val) n.219A>G | |
17 | g.41583918T>G | CA399477716 | KRT14 | c.769A>C (p.Met257Leu) n.219A>C | |
17 | g.41583919C>A | CA399477717 | KRT14 | c.768G>T (p.Glu256Asp) n.218G>T | |
17 | g.41583919C>G | CA399477718 | KRT14 | c.768G>C (p.Glu256Asp) n.218G>C | |
17 | g.41583919C>T | CA500205748 | KRT14 | c.768G>A (p.Glu256=) n.218G>A | |
17 | g.41583920T>A | CA399477719 | KRT14 | c.767A>T (p.Glu256Val) n.217A>T | gnomAD v4 |
17 | g.41583920T>C | CA399477720 | KRT14 | c.767A>G (p.Glu256Gly) n.217A>G | |
17 | g.41583920T>G | CA399477721 | KRT14 | c.767A>C (p.Glu256Ala) n.217A>C | |
17 | g.41583921C>A | CA8562609 | KRT14 | c.766G>T (p.Glu256Ter) n.216G>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.41583921C= | CA2260085622 | KRT14 | c.766G= (p.Glu256=) n.216G= | |
17 | g.41583921C>G | CA399477723 | KRT14 | c.766G>C (p.Glu256Gln) n.216G>C | dbSNP |
17 | g.41583921C>T | CA399477722 | KRT14 | c.766G>A (p.Glu256Lys) n.216G>A | |
17 | g.41583922C>A | CA399477724 | KRT14 | c.766-1G>T (n.766-1G>T) n.216-1G>T | |
17 | g.41583922C>G | CA399477725 | KRT14 | c.766-1G>C (n.766-1G>C) n.216-1G>C | |
17 | g.41583922C>T | CA399477726 | KRT14 | c.766-1G>A (n.766-1G>A) n.216-1G>A | |
17 | g.41583923T>A | CA399477727 | KRT14 | c.766-2A>T (n.766-2A>T) n.216-2A>T | COSMIC |
17 | g.41583923T>C | CA399477728 | KRT14 | c.766-2A>G (n.766-2A>G) n.216-2A>G | |
17 | g.41583923T>G | CA399477729 | KRT14 | c.766-2A>C (n.766-2A>C) n.216-2A>C | |
17 | g.41583924G>C | CA772039261 | KRT14 | c.766-3C>G (n.766-3C>G) n.216-3C>G | dbSNP |
17 | g.41583924G= | CA2260085623 | KRT14 | c.766-3C= (n.766-3C=) n.216-3C= | |
17 | g.41583924G>T | CA8562610 | KRT14 | c.766-3C>A (n.766-3C>A) n.216-3C>A | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.41583927_41583931dup | CA2637835395 | KRT14 | c.766-10_766-6dup (n.766-10_766-6dup) n.216-10_216-6dup | gnomAD v4 |
17 | g.41583930C= | CA2260085624 | KRT14 | c.766-9G= (n.766-9G=) n.216-9G= | |
17 | g.41583930C>T | CA626215404 | KRT14 | c.766-9G>A (n.766-9G>A) n.216-9G>A | dbSNP gnomAD v2 gnomAD v4 |
17 | g.41583931C>A | CA772039263 | KRT14 | c.766-10G>T (n.766-10G>T) n.216-10G>T | dbSNP gnomAD v3 gnomAD v4 |
17 | g.41583931C= | CA2260085625 | KRT14 | c.766-10G= (n.766-10G=) n.216-10G= | |
17 | g.41583931C>T | CA2637835403 | KRT14 | c.766-10G>A (n.766-10G>A) n.216-10G>A | gnomAD v4 |
17 | g.41583932A>G | CA2637835409 | KRT14 | c.766-11T>C (n.766-11T>C) n.216-11T>C | gnomAD v4 |
17 | g.41583933G>A | CA2637835410 | KRT14 | c.766-12C>T (n.766-12C>T) n.216-12C>T | gnomAD v4 |
17 | g.41583934G>A | CA2637835412 | KRT14 | c.766-13C>T (n.766-13C>T) n.216-13C>T | gnomAD v4 |
17 | g.41583936A>G | CA2637835414 | KRT14 | c.766-15T>C (n.766-15T>C) n.216-15T>C | gnomAD v4 |
17 | g.41583937C= | CA2260085626 | KRT14 | c.766-16G= (n.766-16G=) n.216-16G= | |
17 | g.41583937C>G | CA2637835416 | KRT14 | c.766-16G>C (n.766-16G>C) n.216-16G>C | gnomAD v4 |
17 | g.41583937C>T | CA772039264 | KRT14 | c.766-16G>A (n.766-16G>A) n.216-16G>A | dbSNP gnomAD v3 gnomAD v4 |
17 | g.41583938A>C | CA2637835419 | KRT14 | c.766-17T>G (n.766-17T>G) n.216-17T>G | gnomAD v4 |
17 | g.41583939G>T | CA2637835420 | KRT14 | c.766-18C>A (n.766-18C>A) n.216-18C>A | gnomAD v4 |
17 | g.41583941C>A | CA2529124089 | KRT14 | c.766-20G>T (n.766-20G>T) n.216-20G>T | |
17 | g.41583941C>G | CA2637835421 | KRT14 | c.766-20G>C (n.766-20G>C) n.216-20G>C | gnomAD v4 |
17 | g.41583942C>A | CA2733826556 | KRT14 | c.766-21G>T (n.766-21G>T) n.216-21G>T | dbSNP |
17 | g.41583942C>G | CA2809495861 | KRT14 | c.766-21G>C (n.766-21G>C) n.216-21G>C | |
17 | g.41583943A>G | CA2637835422 | KRT14 | c.766-22T>C (n.766-22T>C) n.216-22T>C | gnomAD v4 |
17 | g.41583944C= | CA2260085627 | KRT14 | c.766-23G= (n.766-23G=) n.216-23G= | |
17 | g.41583944C>T | CA290665051 | KRT14 | c.766-23G>A (n.766-23G>A) n.216-23G>A | dbSNP |
17 | g.41583945A>C | CA2637835425 | KRT14 | c.766-24T>G (n.766-24T>G) n.216-24T>G | gnomAD v4 |
17 | g.41583945A>T | CA2637835426 | KRT14 | c.766-24T>A (n.766-24T>A) n.216-24T>A | gnomAD v4 |
17 | g.41583946G>C | CA290665053 | KRT14 | c.766-25C>G (n.766-25C>G) n.216-25C>G | dbSNP gnomAD v4 |
17 | g.41583946G= | CA2260085628 | KRT14 | c.766-25C= (n.766-25C=) n.216-25C= | |
17 | g.41583948C>T | CA2637835430 | KRT14 | c.766-27G>A (n.766-27G>A) n.216-27G>A | gnomAD v4 |
17 | g.41583949A= | CA2260085629 | KRT14 | c.766-28T= (n.766-28T=) n.216-28T= | |
17 | g.41583949A>C | CA2260085630 | KRT14 | c.766-28T>G (n.766-28T>G) n.216-28T>G | dbSNP |
17 | g.41583950G>A | CA2260085632 | KRT14 | c.766-29C>T (n.766-29C>T) n.216-29C>T | dbSNP gnomAD v4 |
17 | g.41583950G= | CA2260085631 | KRT14 | c.766-29C= (n.766-29C=) n.216-29C= | |
17 | g.41583951G>A | CA2637835431 | KRT14 | c.766-30C>T (n.766-30C>T) n.216-30C>T | gnomAD v4 |
17 | g.41583951G>C | CA2637835432 | KRT14 | c.766-30C>G (n.766-30C>G) n.216-30C>G | gnomAD v4 |
17 | g.41583953G>A | CA2260085634 | KRT14 | c.766-32C>T (n.766-32C>T) n.216-32C>T | dbSNP gnomAD v4 |
17 | g.41583953G= | CA2260085633 | KRT14 | c.766-32C= (n.766-32C=) n.216-32C= | |
17 | g.41583955T>A | CA626215405 | KRT14 | c.766-34A>T (n.766-34A>T) n.216-34A>T | dbSNP gnomAD v2 gnomAD v4 |
17 | g.41583955T>C | CA626215406 | KRT14 | c.766-34A>G (n.766-34A>G) n.216-34A>G | dbSNP gnomAD v2 gnomAD v4 |
17 | g.41583955T>G | CA8562611 | KRT14 | c.766-34A>C (n.766-34A>C) n.216-34A>C | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.41583955T= | CA2260085635 | KRT14 | c.766-34A= (n.766-34A=) n.216-34A= | |
17 | g.41583956C>G | CA2637835435 | KRT14 | c.766-35G>C (n.766-35G>C) n.216-35G>C | gnomAD v4 |
17 | g.41583956C>T | CA2839859632 | KRT14 | c.766-35G>A (n.766-35G>A) n.216-35G>A | |
17 | g.41583957C>T | CA2809495864 | KRT14 | c.766-36G>A (n.766-36G>A) n.216-36G>A | |
17 | g.41583958A>T | CA2843324279 | KRT14 | c.766-37T>A (n.766-37T>A) n.216-37T>A | |
17 | g.41583958_41583959delinsAC | CA2260085636 | KRT14 | c.766-38_766-37delinsGT (n.766-38_766-37delinsGT) n.216-38_216-37delinsGT | |
17 | g.41583959C= | CA2260085637 | KRT14 | c.766-38G= (n.766-38G=) n.216-38G= | |
17 | g.41583959C>G | CA626215407 | KRT14 | c.766-38G>C (n.766-38G>C) n.216-38G>C | dbSNP gnomAD v2 gnomAD v4 |
17 | g.41583960del | CA8562612 | KRT14 | c.766-38del (n.766-38del) n.216-38del | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.41583960C>A | CA2843324280 | KRT14 | c.766-39G>T (n.766-39G>T) n.216-39G>T | |
17 | g.41583962T>A | CA2637835439 | KRT14 | c.766-41A>T (n.766-41A>T) n.216-41A>T | gnomAD v4 |
17 | g.41583962T>C | CA2637835441 | KRT14 | c.766-41A>G (n.766-41A>G) n.216-41A>G | gnomAD v4 |
17 | g.41583964G>A | CA2637835442 | KRT14 | c.766-43C>T (n.766-43C>T) n.216-43C>T | gnomAD v4 |
17 | g.41583964G>T | CA2637835444 | KRT14 | c.766-43C>A (n.766-43C>A) n.216-43C>A | gnomAD v4 |
17 | g.41583965C>T | CA2637835445 | KRT14 | c.766-44G>A (n.766-44G>A) n.216-44G>A | gnomAD v4 |
17 | g.41583966A= | CA2260085638 | KRT14 | c.766-45T= (n.766-45T=) n.216-45T= | |
17 | g.41583966A>C | CA8562613 | KRT14 | c.766-45T>G (n.766-45T>G) n.216-45T>G | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.41583966A>G | CA983757829 | KRT14 | c.766-45T>C (n.766-45T>C) n.216-45T>C | dbSNP gnomAD v3 gnomAD v4 |