Chr Mutation (hg38) CAid Gene Transcript Linkouts
17g.41583679_41583761delCA2809495833KRT14c.927+1_928-1del
n.377+1_378-1del
17g.41583721C>ACA983757667KRT14c.927+39G>T (n.927+39G>T)
n.377+39G>T
dbSNP gnomAD v3 gnomAD v4
17g.41583721C=CA2260085538KRT14c.927+39G= (n.927+39G=)
n.377+39G=
17g.41583721_41583725delCA2559752918KRT14c.927+35_927+39del (n.927+35_927+39del)
n.377+35_377+39del
17g.41583723G>ACA2260085540KRT14c.927+37C>T (n.927+37C>T)
n.377+37C>T
dbSNP gnomAD v4
17g.41583723G>CCA2637835098KRT14c.927+37C>G (n.927+37C>G)
n.377+37C>G
gnomAD v4
17g.41583723G=CA2260085539KRT14c.927+37C= (n.927+37C=)
n.377+37C=
17g.41583725delCA2537663325KRT14c.927+35del (n.927+35del)
n.377+35del
17g.41583725T>ACA2733646328KRT14c.927+35A>T (n.927+35A>T)
n.377+35A>T
dbSNP
17g.41583725T>CCA8562572KRT14c.927+35A>G (n.927+35A>G)
n.377+35A>G
dbSNP ExAC
17g.41583725T=CA2260085541KRT14c.927+35A= (n.927+35A=)
n.377+35A=
17g.41583726G>ACA2637835101KRT14c.927+34C>T (n.927+34C>T)
n.377+34C>T
gnomAD v4
17g.41583727G>ACA2260085543KRT14c.927+33C>T (n.927+33C>T)
n.377+33C>T
dbSNP gnomAD v4
17g.41583727G=CA2260085542KRT14c.927+33C= (n.927+33C=)
n.377+33C=
17g.41583728_41583735delCA2563714199KRT14c.927+25_927+32del (n.927+25_927+32del)
n.377+25_377+32del
17g.41583728_41583729insTCCA2569711940KRT14c.927+31_927+32insGA (n.927+31_927+32insGA)
n.377+31_377+32insGA
17g.41583731G>ACA290664991KRT14c.927+29C>T (n.927+29C>T)
n.377+29C>T
dbSNP gnomAD v4
17g.41583731G=CA2260085544KRT14c.927+29C= (n.927+29C=)
n.377+29C=
17g.41583731G>TCA2576267618KRT14c.927+29C>A (n.927+29C>A)
n.377+29C>A
17g.41583732G>ACA8562573KRT14c.927+28C>T (n.927+28C>T)
n.377+28C>T
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.41583732G=CA2260085545KRT14c.927+28C= (n.927+28C=)
n.377+28C=
17g.41583734T>ACA2637835105KRT14c.927+26A>T (n.927+26A>T)
n.377+26A>T
gnomAD v4
17g.41583736C=CA2260085546KRT14c.927+24G= (n.927+24G=)
n.377+24G=
17g.41583736C>GCA2260085547KRT14c.927+24G>C (n.927+24G>C)
n.377+24G>C
dbSNP gnomAD v4
17g.41583736C>TCA2576267619KRT14c.927+24G>A (n.927+24G>A)
n.377+24G>A
17g.41583737C=CA2260085548KRT14c.927+23G= (n.927+23G=)
n.377+23G=
17g.41583737C>TCA8562574KRT14c.927+23G>A (n.927+23G>A)
n.377+23G>A
dbSNP ExAC gnomAD v2 gnomAD v4
17g.41583738T>CCA8562575KRT14c.927+22A>G (n.927+22A>G)
n.377+22A>G
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.41583738T>GCA656360500KRT14c.927+22A>C (n.927+22A>C)
n.377+22A>C
COSMIC COSMIC
17g.41583738T=CA2260085549KRT14c.927+22A= (n.927+22A=)
n.377+22A=
17g.41583739T>CCA2637835113KRT14c.927+21A>G (n.927+21A>G)
n.377+21A>G
gnomAD v4
17g.41583741C>TCA2809495842KRT14c.927+19G>A (n.927+19G>A)
n.377+19G>A
17g.41583742A=CA2260085550KRT14c.927+18T= (n.927+18T=)
n.377+18T=
17g.41583742A>CCA2260085551KRT14c.927+18T>G (n.927+18T>G)
n.377+18T>G
dbSNP
17g.41583742A>GCA772038887KRT14c.927+18T>C (n.927+18T>C)
n.377+18T>C
dbSNP gnomAD v3 gnomAD v4
17g.41583743C=CA2260085552KRT14c.927+17G= (n.927+17G=)
n.377+17G=
17g.41583743C>GCA8562576KRT14c.927+17G>C (n.927+17G>C)
n.377+17G>C
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.41583743C>TCA2260085553KRT14c.927+17G>A (n.927+17G>A)
n.377+17G>A
dbSNP
17g.41583744C=CA2260085554KRT14c.927+16G= (n.927+16G=)
n.377+16G=
17g.41583744C>GCA2809495844KRT14c.927+16G>C (n.927+16G>C)
n.377+16G>C
17g.41583744C>TCA8562577KRT14c.927+16G>A (n.927+16G>A)
n.377+16G>A
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.41583745T>CCA8562578KRT14c.927+15A>G (n.927+15A>G)
n.377+15A>G
dbSNP ExAC gnomAD v2 gnomAD v4
17g.41583745T=CA2260085555KRT14c.927+15A= (n.927+15A=)
n.377+15A=
17g.41583746C=CA2260085556KRT14c.927+14G= (n.927+14G=)
n.377+14G=
17g.41583746C>GCA290665000KRT14c.927+14G>C (n.927+14G>C)
n.377+14G>C
dbSNP gnomAD v3 gnomAD v4
17g.41583747A>GCA2637835123KRT14c.927+13T>C (n.927+13T>C)
n.377+13T>C
gnomAD v4
17g.41583749delCA2637835121KRT14c.927+13del (n.927+13del)
n.377+13del
gnomAD v4
17g.41583753C=CA2260085557KRT14c.927+7G= (n.927+7G=)
n.377+7G=
17g.41583753C>TCA626215403KRT14c.927+7G>A (n.927+7G>A)
n.377+7G>A
dbSNP gnomAD v2 gnomAD v4
17g.41583754A>GCA2637835129KRT14c.927+6T>C (n.927+6T>C)
n.377+6T>C
gnomAD v4
17g.41583755C>ACA2637835133KRT14c.927+5G>T (n.927+5G>T)
n.377+5G>T
gnomAD v4
17g.41583755C>TCA2637835137KRT14c.927+5G>A (n.927+5G>A)
n.377+5G>A
gnomAD v4
17g.41583756C>ACA2637835139KRT14c.927+4G>T (n.927+4G>T)
n.377+4G>T
gnomAD v4
17g.41583756C>GCA2637835140KRT14c.927+4G>C (n.927+4G>C)
n.377+4G>C
gnomAD v4
17g.41583757C>TCA2637835141KRT14c.927+3G>A (n.927+3G>A)
n.377+3G>A
gnomAD v4
17g.41583758A>CCA399476991KRT14c.927+2T>G (n.927+2T>G)
n.377+2T>G
17g.41583758A>GCA399476994KRT14c.927+2T>C (n.927+2T>C)
n.377+2T>C
17g.41583758A>TCA399476996KRT14c.927+2T>A (n.927+2T>A)
n.377+2T>A
17g.41583759C>ACA216993KRT14c.927+1G>T (n.927+1G>T)
n.377+1G>T
ClinVar dbSNP
17g.41583759C=CA2260085558KRT14c.927+1G= (n.927+1G=)
n.377+1G=
17g.41583759C>GCA290665004KRT14c.927+1G>C (n.927+1G>C)
n.377+1G>C
dbSNP
17g.41583759C>TCA216992KRT14c.927+1G>A (n.927+1G>A)
n.377+1G>A
ClinVar dbSNP COSMIC
17g.41583760C>ACA399477005KRT14c.927G>T (p.Lys309Asn)
n.377G>T
17g.41583760C=CA2260085559KRT14c.927G= (p.Lys309=)
n.377G=
17g.41583760C>GCA399477002KRT14c.927G>C (p.Lys309Asn)
n.377G>C
gnomAD v4
17g.41583760C>TCA8562579KRT14c.927G>A (p.Lys309=)
n.377G>A
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.41583761T>ACA399477008KRT14c.926A>T (p.Lys309Met)
n.376A>T
17g.41583761T>CCA399477010KRT14c.926A>G (p.Lys309Arg)
n.376A>G
17g.41583761T>GCA399477012KRT14c.926A>C (p.Lys309Thr)
n.376A>C
17g.41583762T>ACA399477014KRT14c.925A>T (p.Lys309Ter)
n.375A>T
17g.41583762T>CCA399477015KRT14c.925A>G (p.Lys309Glu)
n.375A>G
17g.41583762T>GCA399477017KRT14c.925A>C (p.Lys309Gln)
n.375A>C
17g.41583763G>ACA8562580KRT14c.924C>T (p.Thr308=)
n.374C>T
dbSNP ExAC gnomAD v3 gnomAD v4
17g.41583763G>CCA500205429KRT14c.924C>G (p.Thr308=)
n.374C>G
17g.41583763G=CA2260085560KRT14c.924C= (p.Thr308=)
n.374C=
17g.41583763G>TCA500205430KRT14c.924C>A (p.Thr308=)
n.374C>A
dbSNP gnomAD v3 gnomAD v4
17g.41583764G>ACA399477018KRT14c.923C>T (p.Thr308Ile)
n.373C>T
gnomAD v4
17g.41583764G>CCA399477021KRT14c.923C>G (p.Thr308Ser)
n.373C>G
17g.41583764G>TCA399477023KRT14c.923C>A (p.Thr308Asn)
n.373C>A
17g.41583765T>ACA399477027KRT14c.922A>T (p.Thr308Ser)
n.372A>T
17g.41583765T>CCA399477028KRT14c.922A>G (p.Thr308Ala)
n.372A>G
17g.41583765T>GCA399477032KRT14c.922A>C (p.Thr308Pro)
n.372A>C
17g.41583766G>ACA500205431KRT14c.921C>T (p.Phe307=)
n.371C>T
dbSNP gnomAD v3 gnomAD v4
17g.41583766G>CCA399477035KRT14c.921C>G (p.Phe307Leu)
n.371C>G
17g.41583766G=CA2260085561KRT14c.921C= (p.Phe307=)
n.371C=
17g.41583766G>TCA399477037KRT14c.921C>A (p.Phe307Leu)
n.371C>A
17g.41583767A>CCA399477041KRT14c.920T>G (p.Phe307Cys)
n.370T>G
17g.41583767A>GCA399477042KRT14c.920T>C (p.Phe307Ser)
n.370T>C
dbSNP gnomAD v3 gnomAD v4
17g.41583767A>TCA399477045KRT14c.920T>A (p.Phe307Tyr)
n.370T>A
17g.41583768A>CCA399477047KRT14c.919T>G (p.Phe307Val)
n.369T>G
17g.41583768A>GCA399477048KRT14c.919T>C (p.Phe307Leu)
n.369T>C
17g.41583768A>TCA399477050KRT14c.919T>A (p.Phe307Ile)
n.369T>A
17g.41583769G>ACA500205435KRT14c.918C>T (p.Phe306=)
n.368C>T
dbSNP gnomAD v4 COSMIC
17g.41583769G>CCA399477053KRT14c.918C>G (p.Phe306Leu)
n.368C>G
17g.41583769G=CA2260085562KRT14c.918C= (p.Phe306=)
n.368C=
17g.41583769G>TCA399477052KRT14c.918C>A (p.Phe306Leu)
n.368C>A
COSMIC
17g.41583770A>CCA399477055KRT14c.917T>G (p.Phe306Cys)
n.367T>G
17g.41583770A>GCA399477057KRT14c.917T>C (p.Phe306Ser)
n.367T>C
17g.41583770A>TCA399477060KRT14c.917T>A (p.Phe306Tyr)
n.367T>A
17g.41583771A>CCA399477064KRT14c.916T>G (p.Phe306Val)
n.366T>G
17g.41583771A>GCA399477066KRT14c.916T>C (p.Phe306Leu)
n.366T>C
17g.41583771A>TCA399477069KRT14c.916T>A (p.Phe306Ile)
n.366T>A
17g.41583772C>ACA399477070KRT14c.915G>T (p.Trp305Cys)
n.365G>T
17g.41583772C=CA2260085563KRT14c.915G= (p.Trp305=)
n.365G=
17g.41583772C>GCA399477074KRT14c.915G>C (p.Trp305Cys)
n.365G>C
17g.41583772C>TCA216990KRT14c.915G>A (p.Trp305Ter)
n.365G>A
ClinVar dbSNP gnomAD v2 gnomAD v4
17g.41583773C>ACA8562581KRT14c.914G>T (p.Trp305Leu)
n.364G>T
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.41583773C=CA2260085564KRT14c.914G= (p.Trp305=)
n.364G=
17g.41583773C>GCA399477079KRT14c.914G>C (p.Trp305Ser)
n.364G>C
17g.41583773C>TCA399477081KRT14c.914G>A (p.Trp305Ter)
n.364G>A
gnomAD v4
17g.41583774A>CCA399477084KRT14c.913T>G (p.Trp305Gly)
n.363T>G
17g.41583774A>GCA399477086KRT14c.913T>C (p.Trp305Arg)
n.363T>C
17g.41583774A>TCA399477088KRT14c.913T>A (p.Trp305Arg)
n.363T>A
17g.41583775T>ACA399477092KRT14c.912A>T (p.Glu304Asp)
n.362A>T
17g.41583775T>CCA500205437KRT14c.912A>G (p.Glu304=)
n.362A>G
gnomAD v4
17g.41583775T>GCA399477094KRT14c.912A>C (p.Glu304Asp)
n.362A>C
17g.41583776T>ACA399477097KRT14c.911A>T (p.Glu304Val)
n.361A>T
17g.41583776T>CCA399477100KRT14c.911A>G (p.Glu304Gly)
n.361A>G
17g.41583776T>GCA399477102KRT14c.911A>C (p.Glu304Ala)
n.361A>C
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
17g.41583776T=CA2260085565KRT14c.911A= (p.Glu304=)
n.361A=
17g.41583777C>ACA399477105KRT14c.910G>T (p.Glu304Ter)
n.360G>T
17g.41583777C>GCA399477107KRT14c.910G>C (p.Glu304Gln)
n.360G>C
17g.41583777C>TCA399477106KRT14c.910G>A (p.Glu304Lys)
n.360G>A
COSMIC
17g.41583778C>ACA399477111KRT14c.909G>T (p.Glu303Asp)
n.359G>T
17g.41583778C>GCA399477112KRT14c.909G>C (p.Glu303Asp)
n.359G>C
17g.41583778C>TCA500205440KRT14c.909G>A (p.Glu303=)
n.359G>A
17g.41583779T>ACA399477114KRT14c.908A>T (p.Glu303Val)
n.358A>T
17g.41583779T>CCA399477116KRT14c.908A>G (p.Glu303Gly)
n.358A>G
17g.41583779T>GCA399477117KRT14c.908A>C (p.Glu303Ala)
n.358A>C
17g.41583780C>ACA399477121KRT14c.907G>T (p.Glu303Ter)
n.357G>T
17g.41583780C=CA2260085566KRT14c.907G= (p.Glu303=)
n.357G=
17g.41583780C>GCA399477123KRT14c.907G>C (p.Glu303Gln)
n.357G>C
17g.41583780C>TCA399477125KRT14c.907G>A (p.Glu303Lys)
n.357G>A
ClinVar dbSNP gnomAD v4 COSMIC
17g.41583781G>ACA8562582KRT14c.906C>T (p.Ala302=)
n.356C>T
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.41583781G>CCA500205442KRT14c.906C>G (p.Ala302=)
n.356C>G
17g.41583781G=CA2260085567KRT14c.906C= (p.Ala302=)
n.356C=
17g.41583781G>TCA500205444KRT14c.906C>A (p.Ala302=)
n.356C>A
gnomAD v4
17g.41583782G>ACA399477127KRT14c.905C>T (p.Ala302Val)
n.355C>T
17g.41583782G>CCA399477128KRT14c.905C>G (p.Ala302Gly)
n.355C>G
17g.41583782G>TCA399477130KRT14c.905C>A (p.Ala302Asp)
n.355C>A
17g.41583783C>ACA399477133KRT14c.904G>T (p.Ala302Ser)
n.354G>T
17g.41583783C>GCA399477134KRT14c.904G>C (p.Ala302Pro)
n.354G>C
17g.41583783C>TCA399477136KRT14c.904G>A (p.Ala302Thr)
n.354G>A
17g.41583784A>CCA399477138KRT14c.903T>G (p.Asp301Glu)
n.353T>G
17g.41583784A>GCA500205452KRT14c.903T>C (p.Asp301=)
n.353T>C
17g.41583784A>TCA399477140KRT14c.903T>A (p.Asp301Glu)
n.353T>A
17g.41583785T>ACA399477144KRT14c.902A>T (p.Asp301Val)
n.352A>T
17g.41583785T>CCA399477146KRT14c.902A>G (p.Asp301Gly)
n.352A>G
gnomAD v4
17g.41583785T>GCA399477148KRT14c.902A>C (p.Asp301Ala)
n.352A>C
17g.41583786C>ACA399477151KRT14c.901G>T (p.Asp301Tyr)
n.351G>T
17g.41583786C>GCA399477152KRT14c.901G>C (p.Asp301His)
n.351G>C
17g.41583786C>TCA399477154KRT14c.901G>A (p.Asp301Asn)
n.351G>A
17g.41583787C>ACA399477157KRT14c.900G>T (p.Lys300Asn)
n.350G>T
17g.41583787C=CA2260085568KRT14c.900G= (p.Lys300=)
n.350G=
17g.41583787C>GCA399477159KRT14c.900G>C (p.Lys300Asn)
n.350G>C
17g.41583787C>TCA290665011KRT14c.900G>A (p.Lys300=)
n.350G>A
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
17g.41583788T>ACA399477164KRT14c.899A>T (p.Lys300Met)
n.349A>T
17g.41583788T>CCA399477165KRT14c.899A>G (p.Lys300Arg)
n.349A>G
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
17g.41583788T>GCA399477166KRT14c.899A>C (p.Lys300Thr)
n.349A>C
17g.41583788T=CA2260085569KRT14c.899A= (p.Lys300=)
n.349A=
17g.41583789T>ACA399477169KRT14c.898A>T (p.Lys300Ter)
n.348A>T
17g.41583789T>CCA399477173KRT14c.898A>G (p.Lys300Glu)
n.348A>G
17g.41583789T>GCA399477170KRT14c.898A>C (p.Lys300Gln)
n.348A>C
17g.41583790G>ACA500205459KRT14c.897C>T (p.Arg299=)
n.347C>T
17g.41583790G>CCA500205461KRT14c.897C>G (p.Arg299=)
n.347C>G
17g.41583790G>TCA500205460KRT14c.897C>A (p.Arg299=)
n.347C>A
17g.41583791C>ACA399477176KRT14c.896G>T (p.Arg299Leu)
n.346G>T
dbSNP gnomAD v3 gnomAD v4
17g.41583791C=CA2260085570KRT14c.896G= (p.Arg299=)
n.346G=
17g.41583791C>GCA399477179KRT14c.896G>C (p.Arg299Pro)
n.346G>C
17g.41583791C>TCA8562583KRT14c.896G>A (p.Arg299His)
n.346G>A
dbSNP ExAC gnomAD v2 gnomAD v4
17g.41583792G>ACA399477184KRT14c.895C>T (p.Arg299Cys)
n.345C>T
dbSNP gnomAD v4
17g.41583792G>CCA399477186KRT14c.895C>G (p.Arg299Gly)
n.345C>G
17g.41583792G=CA2260085571KRT14c.895C= (p.Arg299=)
n.345C=
17g.41583792G>TCA399477189KRT14c.895C>A (p.Arg299Ser)
n.345C>A
17g.41583793G>ACA500205468KRT14c.894C>T (p.Asn298=)
n.344C>T
gnomAD v4
17g.41583793G>CCA399477191KRT14c.894C>G (p.Asn298Lys)
n.344C>G
17g.41583793G>TCA399477192KRT14c.894C>A (p.Asn298Lys)
n.344C>A
17g.41583794T>ACA399477196KRT14c.893A>T (p.Asn298Ile)
n.343A>T
17g.41583794T>CCA399477198KRT14c.893A>G (p.Asn298Ser)
n.343A>G
17g.41583794T>GCA399477200KRT14c.893A>C (p.Asn298Thr)
n.343A>C
17g.41583795T>ACA399477209KRT14c.892A>T (p.Asn298Tyr)
n.342A>T
17g.41583795T>CCA399477207KRT14c.892A>G (p.Asn298Asp)
n.342A>G
17g.41583795T>GCA399477204KRT14c.892A>C (p.Asn298His)
n.342A>C
17g.41583796C>ACA399477212KRT14c.891G>T (p.Lys297Asn)
n.341G>T
17g.41583796C>GCA399477215KRT14c.891G>C (p.Lys297Asn)
n.341G>C
17g.41583796C>TCA500205470KRT14c.891G>A (p.Lys297=)
n.341G>A
17g.41583797T>ACA399477216KRT14c.890A>T (p.Lys297Met)
n.340A>T
17g.41583797T>CCA399477217KRT14c.890A>G (p.Lys297Arg)
n.340A>G
gnomAD v4
17g.41583797T>GCA399477218KRT14c.890A>C (p.Lys297Thr)
n.340A>C
17g.41583798T>ACA399477221KRT14c.889A>T (p.Lys297Ter)
n.339A>T
17g.41583798T>CCA399477223KRT14c.889A>G (p.Lys297Glu)
n.339A>G
17g.41583798T>GCA399477225KRT14c.889A>C (p.Lys297Gln)
n.339A>C
17g.41583799C>ACA399477228KRT14c.888G>T (p.Glu296Asp)
n.338G>T
COSMIC
17g.41583799C=CA2260085572KRT14c.888G= (p.Glu296=)
n.338G=
17g.41583799C>GCA399477230KRT14c.888G>C (p.Glu296Asp)
n.338G>C
17g.41583799C>TCA500205473KRT14c.888G>A (p.Glu296=)
n.338G>A
dbSNP
17g.41583800T>ACA399477233KRT14c.887A>T (p.Glu296Val)
n.337A>T
17g.41583800T>CCA399477235KRT14c.887A>G (p.Glu296Gly)
n.337A>G
17g.41583800T>GCA399477237KRT14c.887A>C (p.Glu296Ala)
n.337A>C
17g.41583801C>ACA399477241KRT14c.886G>T (p.Glu296Ter)
n.336G>T
17g.41583801C>GCA399477244KRT14c.886G>C (p.Glu296Gln)
n.336G>C
17g.41583801C>TCA399477240KRT14c.886G>A (p.Glu296Lys)
n.336G>A
gnomAD v4
17g.41583802T>ACA500205475KRT14c.885A>T (p.Ala295=)
n.335A>T
17g.41583802T>CCA500205476KRT14c.885A>G (p.Ala295=)
n.335A>G
17g.41583802T>GCA500205479KRT14c.885A>C (p.Ala295=)
n.335A>C
17g.41583803G>ACA399477250KRT14c.884C>T (p.Ala295Val)
n.334C>T
17g.41583803G>CCA399477248KRT14c.884C>G (p.Ala295Gly)
n.334C>G
17g.41583803G=CA2260085573KRT14c.884C= (p.Ala295=)
n.334C=
17g.41583803G>TCA399477252KRT14c.884C>A (p.Ala295Glu)
n.334C>A
dbSNP
17g.41583804C>ACA399477255KRT14c.883G>T (p.Ala295Ser)
n.333G>T
17g.41583804C>GCA399477257KRT14c.883G>C (p.Ala295Pro)
n.333G>C
17g.41583804C>TCA399477259KRT14c.883G>A (p.Ala295Thr)
n.333G>A
17g.41583805C>ACA399477263KRT14c.882G>T (p.Met294Ile)
n.332G>T
17g.41583805C>GCA399477265KRT14c.882G>C (p.Met294Ile)
n.332G>C
17g.41583805C>TCA399477267KRT14c.882G>A (p.Met294Ile)
n.332G>A
17g.41583806A=CA2260085574KRT14c.881T= (p.Met294=)
n.331T=
17g.41583806A>CCA399477275KRT14c.881T>G (p.Met294Arg)
n.331T>G
17g.41583806A>GCA8562584KRT14c.881T>C (p.Met294Thr)
n.331T>C
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.41583806A>TCA399477273KRT14c.881T>A (p.Met294Lys)
n.331T>A
gnomAD v4
17g.41583807T>ACA399477278KRT14c.880A>T (p.Met294Leu)
n.330A>T
17g.41583807T>CCA399477280KRT14c.880A>G (p.Met294Val)
n.330A>G
dbSNP gnomAD v3 gnomAD v4
17g.41583807T>GCA399477282KRT14c.880A>C (p.Met294Leu)
n.330A>C
17g.41583807T=CA2260085575KRT14c.880A= (p.Met294=)
n.330A=
17g.41583808C>ACA399477284KRT14c.879G>T (p.Lys293Asn)
n.329G>T
17g.41583808C>GCA399477286KRT14c.879G>C (p.Lys293Asn)
n.329G>C
17g.41583808C>TCA500205492KRT14c.879G>A (p.Lys293=)
n.329G>A
17g.41583809T>ACA399477289KRT14c.878A>T (p.Lys293Met)
n.328A>T
17g.41583809T>CCA399477293KRT14c.878A>G (p.Lys293Arg)
n.328A>G
dbSNP gnomAD v2 gnomAD v4
17g.41583809T>GCA399477291KRT14c.878A>C (p.Lys293Thr)
n.328A>C
17g.41583809T=CA2260085576KRT14c.878A= (p.Lys293=)
n.328A=
17g.41583810T>ACA399477296KRT14c.877A>T (p.Lys293Ter)
n.327A>T
17g.41583810T>CCA399477297KRT14c.877A>G (p.Lys293Glu)
n.327A>G
gnomAD v4
17g.41583810T>GCA399477298KRT14c.877A>C (p.Lys293Gln)
n.327A>C
17g.41583811C>ACA399477301KRT14c.876G>T (p.Glu292Asp)
n.326G>T
17g.41583811C>GCA399477303KRT14c.876G>C (p.Glu292Asp)
n.326G>C
17g.41583811C>TCA500205498KRT14c.876G>A (p.Glu292=)
n.326G>A
gnomAD v4
17g.41583812T>ACA399477305KRT14c.875A>T (p.Glu292Val)
n.325A>T
17g.41583812T>CCA399477306KRT14c.875A>G (p.Glu292Gly)
n.325A>G
17g.41583812T>GCA399477308KRT14c.875A>C (p.Glu292Ala)
n.325A>C
17g.41583813C>ACA399477311KRT14c.874G>T (p.Glu292Ter)
n.324G>T
17g.41583813C=CA2260085577KRT14c.874G= (p.Glu292=)
n.324G=
17g.41583813C>GCA399477313KRT14c.874G>C (p.Glu292Gln)
n.324G>C
17g.41583813C>TCA8562585KRT14c.874G>A (p.Glu292Lys)
n.324G>A
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.41583814A>CCA399477317KRT14c.873T>G (p.Tyr291Ter)
n.323T>G
17g.41583814A>GCA500205503KRT14c.873T>C (p.Tyr291=)
n.323T>C
gnomAD v4
17g.41583814A>TCA399477320KRT14c.873T>A (p.Tyr291Ter)
n.323T>A
17g.41583815T>ACA399477323KRT14c.872A>T (p.Tyr291Phe)
n.322A>T
17g.41583815T>CCA8562586KRT14c.872A>G (p.Tyr291Cys)
n.322A>G
dbSNP ExAC gnomAD v2 gnomAD v4
17g.41583815T>GCA399477327KRT14c.872A>C (p.Tyr291Ser)
n.322A>C
gnomAD v4
17g.41583815T=CA2260085578KRT14c.872A= (p.Tyr291=)
n.322A=
17g.41583816A>CCA399477330KRT14c.871T>G (p.Tyr291Asp)
n.321T>G
17g.41583816A>GCA399477332KRT14c.871T>C (p.Tyr291His)
n.321T>C
gnomAD v4
17g.41583816A>TCA399477334KRT14c.871T>A (p.Tyr291Asn)
n.321T>A
17g.41583817C>ACA399477336KRT14c.870G>T (p.Gln290His)
n.320G>T
17g.41583817C=CA2260085579KRT14c.870G= (p.Gln290=)
n.320G=
17g.41583817C>GCA399477337KRT14c.870G>C (p.Gln290His)
n.320G>C
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
17g.41583817C>TCA500205513KRT14c.870G>A (p.Gln290=)
n.320G>A
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
17g.41583818T>ACA8562587KRT14c.869A>T (p.Gln290Leu)
n.319A>T
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.41583818T>CCA399477341KRT14c.869A>G (p.Gln290Arg)
n.319A>G
17g.41583818T>GCA399477343KRT14c.869A>C (p.Gln290Pro)
n.319A>C
17g.41583818T=CA2260085580KRT14c.869A= (p.Gln290=)
n.319A=
17g.41583819G>ACA399477347KRT14c.868C>T (p.Gln290Ter)
n.318C>T
17g.41583819G>CCA399477350KRT14c.868C>G (p.Gln290Glu)
n.318C>G
17g.41583819G>TCA399477352KRT14c.868C>A (p.Gln290Lys)
n.318C>A
17g.41583820G>ACA500205518KRT14c.867C>T (p.Asp289=)
n.317C>T
dbSNP
17g.41583820G>CCA399477355KRT14c.867C>G (p.Asp289Glu)
n.317C>G
17g.41583820G=CA2260085581KRT14c.867C= (p.Asp289=)
n.317C=
17g.41583820G>TCA399477357KRT14c.867C>A (p.Asp289Glu)
n.317C>A
17g.41583821T>ACA399477360KRT14c.866A>T (p.Asp289Val)
n.316A>T
17g.41583821T>CCA399477362KRT14c.866A>G (p.Asp289Gly)
n.316A>G
gnomAD v4
17g.41583821T>GCA399477364KRT14c.866A>C (p.Asp289Ala)
n.316A>C

Number of alleles fetched