Chr Mutation (hg38) CAid Gene Transcript Linkouts
17g.41586341T>ACA399481839KRT14c.494A>T (p.Tyr165Phe)
dbSNP gnomAD v2 gnomAD v4
17g.41586341T>CCA399481842KRT14c.494A>G (p.Tyr165Cys)
17g.41586341T>GCA399481844KRT14c.494A>C (p.Tyr165Ser)
17g.41586341T=CA2260086771KRT14c.494A= (p.Tyr165=)
17g.41586342A>CCA399481846KRT14c.493T>G (p.Tyr165Asp)
17g.41586342A>GCA399481849KRT14c.493T>C (p.Tyr165His)
17g.41586342A>TCA399481851KRT14c.493T>A (p.Tyr165Asn)
17g.41586343G>ACA499991714KRT14c.492C>T (p.Pro164=)
gnomAD v4
17g.41586343G>CCA499991717KRT14c.492C>G (p.Pro164=)
gnomAD v4
17g.41586343G>TCA499991715KRT14c.492C>A (p.Pro164=)
17g.41586344G>ACA399481855KRT14c.491C>T (p.Pro164Leu)
gnomAD v4
17g.41586344G>CCA399481857KRT14c.491C>G (p.Pro164Arg)
17g.41586344G>TCA399481860KRT14c.491C>A (p.Pro164His)
17g.41586345G>ACA399481864KRT14c.490C>T (p.Pro164Ser)
17g.41586345G>CCA399481866KRT14c.490C>G (p.Pro164Ala)
17g.41586345G>TCA399481862KRT14c.490C>A (p.Pro164Thr)
gnomAD v4
17g.41586346A>CCA399481869KRT14c.489T>G (p.Ser163Arg)
17g.41586346A>GCA499991730KRT14c.489T>C (p.Ser163=)
17g.41586346A>TCA399481871KRT14c.489T>A (p.Ser163Arg)
17g.41586347C>ACA399481873KRT14c.488G>T (p.Ser163Ile)
17g.41586347C>GCA399481875KRT14c.488G>C (p.Ser163Thr)
17g.41586347C>TCA399481877KRT14c.488G>A (p.Ser163Asn)
gnomAD v4
17g.41586348T>ACA399481880KRT14c.487A>T (p.Ser163Cys)
17g.41586348T>CCA399481883KRT14c.487A>G (p.Ser163Gly)
17g.41586348T>GCA399481886KRT14c.487A>C (p.Ser163Arg)
17g.41586349G>ACA499991744KRT14c.486C>T (p.Tyr162=)
gnomAD v4
17g.41586349G>CCA399481888KRT14c.486C>G (p.Tyr162Ter)
17g.41586349G>TCA399481890KRT14c.486C>A (p.Tyr162Ter)
17g.41586350T>ACA399481893KRT14c.485A>T (p.Tyr162Phe)
17g.41586350T>CCA399481895KRT14c.485A>G (p.Tyr162Cys)
17g.41586350T>GCA399481896KRT14c.485A>C (p.Tyr162Ser)
17g.41586351A=CA2260086772KRT14c.484T= (p.Tyr162=)
17g.41586351A>CCA399481904KRT14c.484T>G (p.Tyr162Asp)
17g.41586351A>GCA399481900KRT14c.484T>C (p.Tyr162His)
gnomAD v4
17g.41586351A>TCA399481902KRT14c.484T>A (p.Tyr162Asn)
dbSNP
17g.41586351dupCA2580093697KRT14c.484dup (p.Tyr162LeufsTer9)
ClinVar
17g.41586352G>ACA8562709KRT14c.483C>T (p.Asp161=)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.41586352G>CCA399481909KRT14c.483C>G (p.Asp161Glu)
17g.41586352G=CA2260086773KRT14c.483C= (p.Asp161=)
17g.41586352G>TCA399481910KRT14c.483C>A (p.Asp161Glu)
17g.41586353T>ACA399481913KRT14c.482A>T (p.Asp161Val)
17g.41586353T>CCA399481915KRT14c.482A>G (p.Asp161Gly)
gnomAD v4
17g.41586353T>GCA399481917KRT14c.482A>C (p.Asp161Ala)
17g.41586354C>ACA399481920KRT14c.481G>T (p.Asp161Tyr)
17g.41586354C>GCA399481922KRT14c.481G>C (p.Asp161His)
17g.41586354C>TCA399481924KRT14c.481G>A (p.Asp161Asn)
17g.41586355T>ACA399481934KRT14c.480A>T (p.Lys160Asn)
17g.41586355T>CCA499991780KRT14c.480A>G (p.Lys160=)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
17g.41586355T>GCA399481937KRT14c.480A>C (p.Lys160Asn)
17g.41586355T=CA2260086774KRT14c.480A= (p.Lys160=)
17g.41586356T>ACA399481943KRT14c.479A>T (p.Lys160Ile)
17g.41586356T>CCA399481941KRT14c.479A>G (p.Lys160Arg)
17g.41586356T>GCA399481939KRT14c.479A>C (p.Lys160Thr)
17g.41586357T>ACA399481945KRT14c.478A>T (p.Lys160Ter)
17g.41586357T>CCA399481949KRT14c.478A>G (p.Lys160Glu)
gnomAD v4
17g.41586357T>GCA399481947KRT14c.478A>C (p.Lys160Gln)
gnomAD v4
17g.41586358G>ACA499991793KRT14c.477C>T (p.Ile159=)
17g.41586358G>CCA399481950KRT14c.477C>G (p.Ile159Met)
COSMIC
17g.41586358G>TCA499991791KRT14c.477C>A (p.Ile159=)
17g.41586359A>CCA399481952KRT14c.476T>G (p.Ile159Ser)
17g.41586359A>GCA399481954KRT14c.476T>C (p.Ile159Thr)
17g.41586359A>TCA399481955KRT14c.476T>A (p.Ile159Asn)
17g.41586360T>ACA399481957KRT14c.475A>T (p.Ile159Phe)
17g.41586360T>CCA399481959KRT14c.475A>G (p.Ile159Val)
gnomAD v4
17g.41586360T>GCA399481961KRT14c.475A>C (p.Ile159Leu)
17g.41586361C>ACA399481963KRT14c.474G>T (p.Glu158Asp)
ClinVar dbSNP gnomAD v2 gnomAD v4 COSMIC
17g.41586361C=CA2260086775KRT14c.474G= (p.Glu158=)
17g.41586361C>GCA399481964KRT14c.474G>C (p.Glu158Asp)
17g.41586361C>TCA8562710KRT14c.474G>A (p.Glu158=)
dbSNP ExAC gnomAD v2 gnomAD v4
17g.41586362T>ACA399481966KRT14c.473A>T (p.Glu158Val)
17g.41586362T>CCA399481967KRT14c.473A>G (p.Glu158Gly)
17g.41586362T>GCA399481969KRT14c.473A>C (p.Glu158Ala)
17g.41586363C>ACA399481971KRT14c.472G>T (p.Glu158Ter)
17g.41586363C>GCA399481976KRT14c.472G>C (p.Glu158Gln)
17g.41586363C>TCA399481972KRT14c.472G>A (p.Glu158Lys)
gnomAD v4
17g.41586364A=CA2260086776KRT14c.471T= (p.Ala157=)
17g.41586364A>CCA499991824KRT14c.471T>G (p.Ala157=)
17g.41586364A>GCA499991826KRT14c.471T>C (p.Ala157=)
17g.41586364A>TCA499991828KRT14c.471T>A (p.Ala157=)
17g.41586364_41586365insCTCA8562711KRT14c.470_471insAG (p.Glu158ValfsTer16)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.41586365G>ACA399481977KRT14c.470C>T (p.Ala157Val)
17g.41586365G>CCA399481978KRT14c.470C>G (p.Ala157Gly)
dbSNP
17g.41586365G=CA2260086778KRT14c.470C= (p.Ala157=)
17g.41586365G>TCA399481980KRT14c.470C>A (p.Ala157Asp)
17g.41586365_41586367delinsCTGCA2739267535KRT14c.468_470delinsCAG (p.Ala157Ser)
ClinVar
17g.41586365_41586367delinsGCACA2260086777KRT14c.468_470delinsTGC (p.Pro156=)
17g.41586366C>ACA399481982KRT14c.469G>T (p.Ala157Ser)
17g.41586366C=CA2260086779KRT14c.469G= (p.Ala157=)
17g.41586366C>GCA8562713KRT14c.469G>C (p.Ala157Pro)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.41586366C>TCA399481984KRT14c.469G>A (p.Ala157Thr)
dbSNP
17g.41586366_41586367delCA8562712KRT14c.468_469del (p.Ala157Ter)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.41586367A=CA2260086780KRT14c.468T= (p.Pro156=)
17g.41586367A>CCA499991836KRT14c.468T>G (p.Pro156=)
17g.41586367A>GCA499991837KRT14c.468T>C (p.Pro156=)
dbSNP
17g.41586367A>TCA499991838KRT14c.468T>A (p.Pro156=)
17g.41586368G>ACA399481987KRT14c.467C>T (p.Pro156Leu)
gnomAD v4
17g.41586368G>CCA399481988KRT14c.467C>G (p.Pro156Arg)
17g.41586368G>TCA399481991KRT14c.467C>A (p.Pro156His)
gnomAD v4
17g.41586369G>ACA399482002KRT14c.466C>T (p.Pro156Ser)
gnomAD v4
17g.41586369G>CCA399482000KRT14c.466C>G (p.Pro156Ala)
17g.41586369G=CA2260086781KRT14c.466C= (p.Pro156=)
17g.41586369G>TCA399481994KRT14c.466C>A (p.Pro156Thr)
dbSNP gnomAD v3 gnomAD v4
17g.41586370C>ACA499991840KRT14c.465G>T (p.Arg155=)
17g.41586370C>GCA499991841KRT14c.465G>C (p.Arg155=)
17g.41586370C>TCA499991842KRT14c.465G>A (p.Arg155=)
17g.41586371C>ACA399482012KRT14c.464G>T (p.Arg155Leu)
17g.41586371C=CA2260086782KRT14c.464G= (p.Arg155=)
17g.41586371C>GCA399482005KRT14c.464G>C (p.Arg155Pro)
dbSNP gnomAD v4
17g.41586371C>TCA8562714KRT14c.464G>A (p.Arg155Gln)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
17g.41586372G>ACA8562715KRT14c.463C>T (p.Arg155Trp)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.41586372G>CCA399482016KRT14c.463C>G (p.Arg155Gly)
17g.41586372G=CA2260086783KRT14c.463C= (p.Arg155=)
17g.41586372G>TCA499991846KRT14c.463C>A (p.Arg155=)
gnomAD v4
17g.41586373C>ACA399482018KRT14c.462G>T (p.Gln154His)
17g.41586373C>GCA399482020KRT14c.462G>C (p.Gln154His)
17g.41586373C>TCA499991848KRT14c.462G>A (p.Gln154=)
17g.41586374T>ACA399482026KRT14c.461A>T (p.Gln154Leu)
17g.41586374T>CCA399482022KRT14c.461A>G (p.Gln154Arg)
17g.41586374T>GCA399482025KRT14c.461A>C (p.Gln154Pro)
17g.41586375G>ACA399482028KRT14c.460C>T (p.Gln154Ter)
17g.41586375G>CCA399482031KRT14c.460C>G (p.Gln154Glu)
dbSNP gnomAD v4
17g.41586375G>TCA399482034KRT14c.460C>A (p.Gln154Lys)
17g.41586376C>ACA399482036KRT14c.459G>T (p.Arg153Ser)
17g.41586376C>GCA399482039KRT14c.459G>C (p.Arg153Ser)
17g.41586376C>TCA499991854KRT14c.459G>A (p.Arg153=)
17g.41586377C>ACA399482042KRT14c.458G>T (p.Arg153Met)
17g.41586377C>GCA399482047KRT14c.458G>C (p.Arg153Thr)
17g.41586377C>TCA399482045KRT14c.458G>A (p.Arg153Lys)
17g.41586378T>ACA399482048KRT14c.457A>T (p.Arg153Trp)
17g.41586378T>CCA399482049KRT14c.457A>G (p.Arg153Gly)
17g.41586378T>GCA499991858KRT14c.457A>C (p.Arg153=)
17g.41586379C>ACA399482051KRT14c.456G>T (p.Gln152His)
17g.41586379C=CA2260086784KRT14c.456G= (p.Gln152=)
17g.41586379C>GCA8562716KRT14c.456G>C (p.Gln152His)
dbSNP ExAC gnomAD v2 gnomAD v4
17g.41586379C>TCA499991860KRT14c.456G>A (p.Gln152=)
17g.41586380T>ACA399482054KRT14c.455A>T (p.Gln152Leu)
17g.41586380T>CCA399482055KRT14c.455A>G (p.Gln152Arg)
17g.41586380T>GCA399482057KRT14c.455A>C (p.Gln152Pro)
17g.41586381G>ACA399482059KRT14c.454C>T (p.Gln152Ter)
gnomAD v4
17g.41586381G>CCA399482061KRT14c.454C>G (p.Gln152Glu)
17g.41586381G>TCA399482063KRT14c.454C>A (p.Gln152Lys)
17g.41586382G>ACA499991864KRT14c.453C>T (p.Tyr151=)
17g.41586382G>CCA399482065KRT14c.453C>G (p.Tyr151Ter)
17g.41586382G>TCA399482067KRT14c.453C>A (p.Tyr151Ter)
17g.41586383T>ACA399482071KRT14c.452A>T (p.Tyr151Phe)
17g.41586383T>CCA399482073KRT14c.452A>G (p.Tyr151Cys)
dbSNP
17g.41586383T>GCA399482069KRT14c.452A>C (p.Tyr151Ser)
17g.41586383T=CA2260086785KRT14c.452A= (p.Tyr151=)
17g.41586384A>CCA399482075KRT14c.451T>G (p.Tyr151Asp)
17g.41586384A>GCA399482077KRT14c.451T>C (p.Tyr151His)
17g.41586384A>TCA399482079KRT14c.451T>A (p.Tyr151Asn)
17g.41586385C>ACA399482081KRT14c.450G>T (p.Trp150Cys)
17g.41586385C>GCA399482083KRT14c.450G>C (p.Trp150Cys)
17g.41586385C>TCA399482085KRT14c.450G>A (p.Trp150Ter)
17g.41586386C>ACA399482091KRT14c.449G>T (p.Trp150Leu)
17g.41586386C>GCA399482087KRT14c.449G>C (p.Trp150Ser)
17g.41586386C>TCA399482089KRT14c.449G>A (p.Trp150Ter)
gnomAD v4
17g.41586386_41586387delCA2637837248KRT14c.448_449del (p.Trp150ValfsTer8)
gnomAD v4
17g.41586387A>CCA399482093KRT14c.448T>G (p.Trp150Gly)
gnomAD v4
17g.41586387A>GCA399482095KRT14c.448T>C (p.Trp150Arg)
17g.41586387A>TCA399482097KRT14c.448T>A (p.Trp150Arg)
17g.41586388G>ACA499991874KRT14c.447C>T (p.Asp149=)
17g.41586388G>CCA399482098KRT14c.447C>G (p.Asp149Glu)
17g.41586388G>TCA399482100KRT14c.447C>A (p.Asp149Glu)
17g.41586389T>ACA399482104KRT14c.446A>T (p.Asp149Val)
17g.41586389T>CCA8562717KRT14c.446A>G (p.Asp149Gly)
dbSNP ExAC gnomAD v2 gnomAD v4
17g.41586389T>GCA399482103KRT14c.446A>C (p.Asp149Ala)
17g.41586389T=CA2260086786KRT14c.446A= (p.Asp149=)
17g.41586390C>ACA399482105KRT14c.445G>T (p.Asp149Tyr)
17g.41586390C>GCA399482106KRT14c.445G>C (p.Asp149His)
17g.41586390C>TCA399482108KRT14c.445G>A (p.Asp149Asn)
17g.41586391A>CCA499991878KRT14c.444T>G (p.Arg148=)
17g.41586391A>GCA499991880KRT14c.444T>C (p.Arg148=)
dbSNP gnomAD v4
17g.41586391A>TCA499991882KRT14c.444T>A (p.Arg148=)
17g.41586392C>ACA399482111KRT14c.443G>T (p.Arg148Leu)
17g.41586392C=CA2260086787KRT14c.443G= (p.Arg148=)
17g.41586392C>GCA399482112KRT14c.443G>C (p.Arg148Pro)
17g.41586392C>TCA399482114KRT14c.443G>A (p.Arg148His)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
17g.41586393G>ACA216961KRT14c.442C>T (p.Arg148Cys)
ClinVar dbSNP gnomAD v4
17g.41586393G>CCA8562718KRT14c.442C>G (p.Arg148Gly)
dbSNP ExAC gnomAD v2 gnomAD v4
17g.41586393G=CA2260086788KRT14c.442C= (p.Arg148=)
17g.41586393G>TCA399482120KRT14c.442C>A (p.Arg148Ser)
COSMIC
17g.41586394G>ACA499991888KRT14c.441C>T (p.Ile147=)
17g.41586394G>CCA399482123KRT14c.441C>G (p.Ile147Met)
17g.41586394G>TCA499991889KRT14c.441C>A (p.Ile147=)
17g.41586395A=CA2260086789KRT14c.440T= (p.Ile147=)
17g.41586395A>CCA399482128KRT14c.440T>G (p.Ile147Ser)
17g.41586395A>GCA399482130KRT14c.440T>C (p.Ile147Thr)
17g.41586395A>TCA399482132KRT14c.440T>A (p.Ile147Asn)
dbSNP gnomAD v4
17g.41586396T>ACA399482134KRT14c.439A>T (p.Ile147Phe)
17g.41586396T>CCA399482138KRT14c.439A>G (p.Ile147Val)
17g.41586396T>GCA399482137KRT14c.439A>C (p.Ile147Leu)
17g.41586397C>ACA399482144KRT14c.438G>T (p.Lys146Asn)
17g.41586397C>GCA399482147KRT14c.438G>C (p.Lys146Asn)
17g.41586397C>TCA499991894KRT14c.438G>A (p.Lys146=)
17g.41586398T>ACA399482150KRT14c.437A>T (p.Lys146Met)
17g.41586398T>CCA399482151KRT14c.437A>G (p.Lys146Arg)
17g.41586398T>GCA399482154KRT14c.437A>C (p.Lys146Thr)
17g.41586399T>ACA399482157KRT14c.436A>T (p.Lys146Ter)
17g.41586399T>CCA399482158KRT14c.436A>G (p.Lys146Glu)
17g.41586399T>GCA399482172KRT14c.436A>C (p.Lys146Gln)
17g.41586400C>ACA499991903KRT14c.435G>T (p.Val145=)
17g.41586400C>GCA499991897KRT14c.435G>C (p.Val145=)
17g.41586400C>TCA499991900KRT14c.435G>A (p.Val145=)
17g.41586401A=CA2260086790KRT14c.434T= (p.Val145=)
17g.41586401A>CCA399482173KRT14c.434T>G (p.Val145Gly)
17g.41586401A>GCA8562719KRT14c.434T>C (p.Val145Ala)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.41586401A>TCA399482180KRT14c.434T>A (p.Val145Glu)
17g.41586402C>ACA399482189KRT14c.433G>T (p.Val145Leu)
17g.41586402C=CA2260086791KRT14c.433G= (p.Val145=)
17g.41586402C>GCA399482186KRT14c.433G>C (p.Val145Leu)
COSMIC
17g.41586402C>TCA399482185KRT14c.433G>A (p.Val145Met)
17g.41586403T>ACA399482192KRT14c.432A>T (p.Glu144Asp)
17g.41586403T>CCA499991907KRT14c.432A>G (p.Glu144=)
17g.41586403T>GCA399482194KRT14c.432A>C (p.Glu144Asp)
17g.41586404dupCA290665551KRT14c.432dup (p.Val145SerfsTer5)
dbSNP
17g.41586404T>ACA399482196KRT14c.431A>T (p.Glu144Val)
17g.41586404T>CCA399482201KRT14c.431A>G (p.Glu144Gly)
17g.41586404T>GCA216959KRT14c.431A>C (p.Glu144Ala)
ClinVar dbSNP
17g.41586404T=CA2260086792KRT14c.431A= (p.Glu144=)
17g.41586405C>ACA399482204KRT14c.430G>T (p.Glu144Ter)
17g.41586405C=CA2260086793KRT14c.430G= (p.Glu144=)
17g.41586405C>GCA399482206KRT14c.430G>C (p.Glu144Gln)
dbSNP gnomAD v2 gnomAD v4
17g.41586405C>TCA399482207KRT14c.430G>A (p.Glu144Lys)
17g.41586406C>ACA499991915KRT14c.429G>T (p.Leu143=)
17g.41586406C>GCA499991917KRT14c.429G>C (p.Leu143=)
17g.41586406C>TCA499991920KRT14c.429G>A (p.Leu143=)
17g.41586407A=CA2260086795KRT14c.428T= (p.Leu143=)
17g.41586407A>CCA399482210KRT14c.428T>G (p.Leu143Arg)
17g.41586407A>GCA216957KRT14c.428T>C (p.Leu143Pro)
ClinVar dbSNP
17g.41586407A>TCA399482214KRT14c.428T>A (p.Leu143Gln)
17g.41586407_41586408delinsAGCA2260086794KRT14c.427_428delinsCT (p.Leu143=)
17g.41586407_41586411delinsAGGTCCA2260086796KRT14c.424_428delinsGACCT (p.Asp142=)
17g.41586408G>ACA290665557KRT14c.427C>T (p.Leu143=)
ClinVar dbSNP gnomAD v4
17g.41586408G>CCA399482229KRT14c.427C>G (p.Leu143Val)
17g.41586408G=CA2260086797KRT14c.427C= (p.Leu143=)
17g.41586408G>TCA399482230KRT14c.427C>A (p.Leu143Met)
17g.41586409delCA216956KRT14c.427del (p.Leu143TrpfsTer3)
ClinVar dbSNP
17g.41586410_41586413delCA8562720KRT14c.424_427del (p.Asp142TrpfsTer3)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.41586409G>ACA8562721KRT14c.426C>T (p.Asp142=)
dbSNP ExAC gnomAD v2 gnomAD v4
17g.41586409G>CCA399482236KRT14c.426C>G (p.Asp142Glu)
dbSNP gnomAD v4
17g.41586409G=CA2260086798KRT14c.426C= (p.Asp142=)
17g.41586409G>TCA399482238KRT14c.426C>A (p.Asp142Glu)
17g.41586410T>ACA399482241KRT14c.425A>T (p.Asp142Val)
17g.41586410T>CCA399482243KRT14c.425A>G (p.Asp142Gly)
17g.41586410T>GCA399482245KRT14c.425A>C (p.Asp142Ala)
dbSNP gnomAD v3 gnomAD v4
17g.41586410T=CA2260086799KRT14c.425A= (p.Asp142=)
17g.41586411C>ACA399482248KRT14c.424G>T (p.Asp142Tyr)
17g.41586411C=CA2260086800KRT14c.424G= (p.Asp142=)
17g.41586411C>GCA399482253KRT14c.424G>C (p.Asp142His)
gnomAD v4
17g.41586411C>TCA8562722KRT14c.424G>A (p.Asp142Asn)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.41586412G>ACA290665562KRT14c.423C>T (p.Ala141=)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
17g.41586412G>CCA499991935KRT14c.423C>G (p.Ala141=)
17g.41586412G=CA2260086801KRT14c.423C= (p.Ala141=)
17g.41586412G>TCA499991936KRT14c.423C>A (p.Ala141=)
gnomAD v4
17g.41586412_41586473delCA645584614KRT14c.362_423del (p.Asn121ArgfsTer8)
COSMIC
17g.41586413G>ACA399482267KRT14c.422C>T (p.Ala141Val)
dbSNP gnomAD v2 gnomAD v4
17g.41586413G>CCA399482269KRT14c.422C>G (p.Ala141Gly)
17g.41586413G=CA2260086802KRT14c.422C= (p.Ala141=)
17g.41586413G>TCA399482272KRT14c.422C>A (p.Ala141Asp)
17g.41586414C>ACA399482279KRT14c.421G>T (p.Ala141Ser)
17g.41586414C=CA2260086803KRT14c.421G= (p.Ala141=)
17g.41586414C>GCA399482277KRT14c.421G>C (p.Ala141Pro)
17g.41586414C>TCA8562723KRT14c.421G>A (p.Ala141Thr)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.41586415G>ACA8562724KRT14c.420C>T (p.Asn140=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.41586415G>CCA399482282KRT14c.420C>G (p.Asn140Lys)
17g.41586415G=CA2260086804KRT14c.420C= (p.Asn140=)
17g.41586415G>TCA399482284KRT14c.420C>A (p.Asn140Lys)
17g.41586416T>ACA399482288KRT14c.419A>T (p.Asn140Ile)
17g.41586416T>CCA216954KRT14c.419A>G (p.Asn140Ser)
ClinVar dbSNP gnomAD v4
17g.41586416T>GCA399482293KRT14c.419A>C (p.Asn140Thr)
17g.41586416T=CA2260086805KRT14c.419A= (p.Asn140=)
17g.41586417T>ACA399482297KRT14c.418A>T (p.Asn140Tyr)
17g.41586417T>CCA399482298KRT14c.418A>G (p.Asn140Asp)
17g.41586417T>GCA399482299KRT14c.418A>C (p.Asn140His)
17g.41586418G>ACA8562726KRT14c.417C>T (p.Ala139=)
dbSNP ExAC gnomAD v2 gnomAD v4
17g.41586418G>CCA8562725KRT14c.417C>G (p.Ala139=)
dbSNP ExAC gnomAD v2 gnomAD v4
17g.41586418G=CA2260086806KRT14c.417C= (p.Ala139=)
17g.41586418G>TCA499991947KRT14c.417C>A (p.Ala139=)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
17g.41586419G>ACA399482306KRT14c.416C>T (p.Ala139Val)
17g.41586419G>CCA399482309KRT14c.416C>G (p.Ala139Gly)
dbSNP gnomAD v3 gnomAD v4
17g.41586419G=CA2260086807KRT14c.416C= (p.Ala139=)
17g.41586419G>TCA399482312KRT14c.416C>A (p.Ala139Asp)
17g.41586420C>ACA399482320KRT14c.415G>T (p.Ala139Ser)
gnomAD v4
17g.41586420C>GCA399482317KRT14c.415G>C (p.Ala139Pro)
ClinVar
17g.41586420C>TCA399482315KRT14c.415G>A (p.Ala139Thr)
gnomAD v4
17g.41586421C>ACA399482323KRT14c.414G>T (p.Glu138Asp)
17g.41586421C>GCA399482324KRT14c.414G>C (p.Glu138Asp)
17g.41586421C>TCA499991953KRT14c.414G>A (p.Glu138=)
17g.41586422T>ACA399482327KRT14c.413A>T (p.Glu138Val)
17g.41586422T>CCA399482330KRT14c.413A>G (p.Glu138Gly)
17g.41586422T>GCA399482332KRT14c.413A>C (p.Glu138Ala)
17g.41586423C>ACA399482334KRT14c.412G>T (p.Glu138Ter)
gnomAD v4
17g.41586423C=CA2260086808KRT14c.412G= (p.Glu138=)
17g.41586423C>GCA399482341KRT14c.412G>C (p.Glu138Gln)
gnomAD v4
17g.41586423C>TCA399482342KRT14c.412G>A (p.Glu138Lys)
dbSNP
17g.41586424C>ACA399482343KRT14c.411G>T (p.Glu137Asp)
17g.41586424C=CA2260086809KRT14c.411G= (p.Glu137=)
17g.41586424C>GCA399482349KRT14c.411G>C (p.Glu137Asp)
17g.41586424C>TCA499991955KRT14c.411G>A (p.Glu137=)
dbSNP
17g.41586425T>ACA399482352KRT14c.410A>T (p.Glu137Val)
17g.41586425T>CCA399482361KRT14c.410A>G (p.Glu137Gly)
17g.41586425T>GCA399482363KRT14c.410A>C (p.Glu137Ala)
17g.41586426C>ACA399482370KRT14c.409G>T (p.Glu137Ter)
gnomAD v4
17g.41586426C>GCA399482368KRT14c.409G>C (p.Glu137Gln)
gnomAD v4
17g.41586426C>TCA399482366KRT14c.409G>A (p.Glu137Lys)
17g.41586427C>ACA499991958KRT14c.408G>T (p.Leu136=)
17g.41586427C>GCA499991962KRT14c.408G>C (p.Leu136=)
17g.41586427C>TCA499991960KRT14c.408G>A (p.Leu136=)
17g.41586428A=CA2260086810KRT14c.407T= (p.Leu136=)
17g.41586428A>CCA399482373KRT14c.407T>G (p.Leu136Arg)
17g.41586428A>GCA216952KRT14c.407T>C (p.Leu136Pro)
ClinVar dbSNP
17g.41586428A>TCA216950KRT14c.407T>A (p.Leu136Gln)
ClinVar dbSNP
17g.41586429G>ACA499991964KRT14c.406C>T (p.Leu136=)
17g.41586429G>CCA399482378KRT14c.406C>G (p.Leu136Val)
17g.41586429G>TCA399482380KRT14c.406C>A (p.Leu136Met)
17g.41586430A>CCA499991970KRT14c.405T>G (p.Ala135=)
17g.41586430A>GCA499991968KRT14c.405T>C (p.Ala135=)
17g.41586430A>TCA499991969KRT14c.405T>A (p.Ala135=)
17g.41586431G>ACA8562727KRT14c.404C>T (p.Ala135Val)
dbSNP ExAC gnomAD v2 gnomAD v4
17g.41586431G>CCA399482383KRT14c.404C>G (p.Ala135Gly)
17g.41586431G=CA2260086811KRT14c.404C= (p.Ala135=)
17g.41586431G>TCA399482387KRT14c.404C>A (p.Ala135Asp)
dbSNP gnomAD v3 gnomAD v4
17g.41586432C>ACA399482390KRT14c.403G>T (p.Ala135Ser)
17g.41586432C>GCA399482392KRT14c.403G>C (p.Ala135Pro)
17g.41586432C>TCA399482395KRT14c.403G>A (p.Ala135Thr)
17g.41586433A=CA2260086812KRT14c.402T= (p.Arg134=)
17g.41586433A>CCA499991973KRT14c.402T>G (p.Arg134=)
17g.41586433A>GCA499991974KRT14c.402T>C (p.Arg134=)
17g.41586433A>TCA499991975KRT14c.402T>A (p.Arg134=)
dbSNP gnomAD v4
17g.41586434C>ACA399482397KRT14c.401G>T (p.Arg134Leu)
17g.41586434C=CA2260086813KRT14c.401G= (p.Arg134=)
17g.41586434C>GCA216948KRT14c.401G>C (p.Arg134Pro)
ClinVar dbSNP
17g.41586434C>TCA399482402KRT14c.401G>A (p.Arg134His)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
17g.41586435G>ACA216946KRT14c.400C>T (p.Arg134Cys)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.41586435G>CCA399482409KRT14c.400C>G (p.Arg134Gly)
17g.41586435G=CA2260086814KRT14c.400C= (p.Arg134=)
17g.41586435G>TCA399482405KRT14c.400C>A (p.Arg134Ser)
17g.41586436C>ACA216944KRT14c.399G>T (p.Val133=)
ClinVar dbSNP
17g.41586436C=CA2260086815KRT14c.399G= (p.Val133=)
17g.41586436C>GCA499991979KRT14c.399G>C (p.Val133=)
17g.41586436C>TCA499991980KRT14c.399G>A (p.Val133=)
17g.41586437A=CA2260086816KRT14c.398T= (p.Val133=)
17g.41586437A>CCA399482418KRT14c.398T>G (p.Val133Gly)
17g.41586437A>GCA216942KRT14c.398T>C (p.Val133Ala)
ClinVar dbSNP gnomAD v4
17g.41586437A>TCA399482415KRT14c.398T>A (p.Val133Glu)
17g.41586438C>ACA216941KRT14c.397G>T (p.Val133Leu)
ClinVar dbSNP
17g.41586438C=CA2260086817KRT14c.397G= (p.Val133=)
17g.41586438C>GCA216939KRT14c.397G>C (p.Val133Leu)
ClinVar dbSNP
17g.41586438C>TCA216937KRT14c.397G>A (p.Val133Met)
ClinVar dbSNP COSMIC
17g.41586439C>ACA399482423KRT14c.396G>T (p.Lys132Asn)
17g.41586439C=CA2260086818KRT14c.396G= (p.Lys132=)
17g.41586439C>GCA399482425KRT14c.396G>C (p.Lys132Asn)
17g.41586439C>TCA8562728KRT14c.396G>A (p.Lys132=)
dbSNP ExAC gnomAD v2 gnomAD v4
17g.41586440T>ACA399482431KRT14c.395A>T (p.Lys132Met)
17g.41586440T>CCA399482434KRT14c.395A>G (p.Lys132Arg)
17g.41586440T>GCA399482436KRT14c.395A>C (p.Lys132Thr)
gnomAD v4
17g.41586441T>ACA399482440KRT14c.394A>T (p.Lys132Ter)
17g.41586441T>CCA399482442KRT14c.394A>G (p.Lys132Glu)
17g.41586441T>GCA399482444KRT14c.394A>C (p.Lys132Gln)

Number of alleles fetched