Chr Mutation (hg38) CAid Gene Transcript Linkouts
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)
17g.41586442G>ACA499991984KRT14c.393C>T (p.Asp131=)
17g.41586442G>CCA399482447KRT14c.393C>G (p.Asp131Glu)
17g.41586442G>TCA399482449KRT14c.393C>A (p.Asp131Glu)
17g.41586443T>ACA399482451KRT14c.392A>T (p.Asp131Val)
17g.41586443T>CCA399482454KRT14c.392A>G (p.Asp131Gly)
17g.41586443T>GCA399482457KRT14c.392A>C (p.Asp131Ala)
17g.41586444C>ACA399482460KRT14c.391G>T (p.Asp131Tyr)
17g.41586444C>GCA399482461KRT14c.391G>C (p.Asp131His)
17g.41586444C>TCA399482464KRT14c.391G>A (p.Asp131Asn)
17g.41586445C>ACA499991985KRT14c.390G>T (p.Leu130=)
17g.41586445C>GCA499991986KRT14c.390G>C (p.Leu130=)
gnomAD v4
17g.41586445C>TCA499991987KRT14c.390G>A (p.Leu130=)
17g.41586446A=CA2260086819KRT14c.389T= (p.Leu130=)
17g.41586446A>CCA399482466KRT14c.389T>G (p.Leu130Arg)
17g.41586446A>GCA216935KRT14c.389T>C (p.Leu130Pro)
ClinVar dbSNP
17g.41586446A>TCA399482468KRT14c.389T>A (p.Leu130Gln)
17g.41586447G>ACA499991989KRT14c.388C>T (p.Leu130=)
17g.41586447G>CCA399482471KRT14c.388C>G (p.Leu130Val)
gnomAD v4
17g.41586447G>TCA399482472KRT14c.388C>A (p.Leu130Met)
17g.41586448G>ACA8562729KRT14c.387C>T (p.Tyr129=)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.41586448G>CCA399482476KRT14c.387C>G (p.Tyr129Ter)
17g.41586448G=CA2260086820KRT14c.387C= (p.Tyr129=)
17g.41586448G>TCA399482474KRT14c.387C>A (p.Tyr129Ter)
17g.41586449T>ACA399482478KRT14c.386A>T (p.Tyr129Phe)
17g.41586449T>CCA216933KRT14c.386A>G (p.Tyr129Cys)
ClinVar dbSNP
17g.41586449T>GCA399482480KRT14c.386A>C (p.Tyr129Ser)
17g.41586449T=CA2260086821KRT14c.386A= (p.Tyr129=)
17g.41586449_41586452delinsTAGGCA2260086822KRT14c.383_386delinsCCTA (p.Ser128=)
17g.41586450A=CA2260086823KRT14c.385T= (p.Tyr129=)
17g.41586450A>CCA216931KRT14c.385T>G (p.Tyr129Asp)
ClinVar dbSNP
17g.41586450A>GCA399482483KRT14c.385T>C (p.Tyr129His)
ClinVar dbSNP
17g.41586450A>TCA399482485KRT14c.385T>A (p.Tyr129Asn)
17g.41586453_41586455delCA216929KRT14c.383_385del (p.Ser128del)
ClinVar dbSNP
17g.41586451G>ACA499991992KRT14c.384C>T (p.Ser128=)
dbSNP
17g.41586451G>CCA499991990KRT14c.384C>G (p.Ser128=)
17g.41586451G=CA2260086824KRT14c.384C= (p.Ser128=)
17g.41586451G>TCA499991991KRT14c.384C>A (p.Ser128=)
17g.41586452G>ACA399482486KRT14c.383C>T (p.Ser128Phe)
17g.41586452G>CCA399482487KRT14c.383C>G (p.Ser128Cys)
17g.41586452G>TCA399482489KRT14c.383C>A (p.Ser128Tyr)
17g.41586453A=CA2260086825KRT14c.382T= (p.Ser128=)
17g.41586453A>CCA399482491KRT14c.382T>G (p.Ser128Ala)
17g.41586453A>GCA216927KRT14c.382T>C (p.Ser128Pro)
ClinVar dbSNP
17g.41586453A>TCA399482493KRT14c.382T>A (p.Ser128Thr)
dbSNP gnomAD v2 gnomAD v4
17g.41586454G>ACA499991993KRT14c.381C>T (p.Ala127=)
dbSNP gnomAD v3 gnomAD v4
17g.41586454G>CCA499991994KRT14c.381C>G (p.Ala127=)
gnomAD v4
17g.41586454G=CA2260086826KRT14c.381C= (p.Ala127=)
17g.41586454G>TCA499991995KRT14c.381C>A (p.Ala127=)
17g.41586455G>ACA399482498KRT14c.380C>T (p.Ala127Val)
COSMIC
17g.41586455G>CCA399482495KRT14c.380C>G (p.Ala127Gly)
17g.41586455G>TCA399482497KRT14c.380C>A (p.Ala127Asp)
COSMIC
17g.41586456C>ACA8562730KRT14c.379G>T (p.Ala127Ser)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.41586456C=CA2260086827KRT14c.379G= (p.Ala127=)
17g.41586456C>GCA399482500KRT14c.379G>C (p.Ala127Pro)
17g.41586456C>TCA399482501KRT14c.379G>A (p.Ala127Thr)
17g.41586457C>ACA499991996KRT14c.378G>T (p.Leu126=)
dbSNP gnomAD v3 gnomAD v4
17g.41586457C=CA2260086828KRT14c.378G= (p.Leu126=)
17g.41586457C>GCA499991997KRT14c.378G>C (p.Leu126=)
17g.41586457C>TCA499991998KRT14c.378G>A (p.Leu126=)
17g.41586458A>CCA399482503KRT14c.377T>G (p.Leu126Arg)
17g.41586458A>GCA399482505KRT14c.377T>C (p.Leu126Pro)
17g.41586458A>TCA399482510KRT14c.377T>A (p.Leu126Gln)
17g.41586459G>ACA8562731KRT14c.376C>T (p.Leu126=)
dbSNP ExAC gnomAD v2 gnomAD v4
17g.41586459G>CCA399482512KRT14c.376C>G (p.Leu126Val)
ClinVar
17g.41586459G=CA2260086829KRT14c.376C= (p.Leu126=)
17g.41586459G>TCA399482513KRT14c.376C>A (p.Leu126Met)
gnomAD v4
17g.41586460G>ACA499991999KRT14c.375C>T (p.Arg125=)
17g.41586460G>CCA499992000KRT14c.375C>G (p.Arg125=)
17g.41586460G>TCA499992001KRT14c.375C>A (p.Arg125=)
17g.41586461C>ACA216925KRT14c.374G>T (p.Arg125Leu)
ClinVar dbSNP
17g.41586461C=CA2260086830KRT14c.374G= (p.Arg125=)
17g.41586461C>GCA216923KRT14c.374G>C (p.Arg125Pro)
ClinVar dbSNP
17g.41586461C>TCA216921KRT14c.374G>A (p.Arg125His)
ClinVar dbSNP gnomAD v4
17g.41586462G>ACA216919KRT14c.373C>T (p.Arg125Cys)
ClinVar dbSNP gnomAD v4
17g.41586462G>CCA216917KRT14c.373C>G (p.Arg125Gly)
ClinVar dbSNP
17g.41586462G=CA2260086831KRT14c.373C= (p.Arg125=)
17g.41586462G>TCA399482518KRT14c.373C>A (p.Arg125Ser)
ClinVar dbSNP
17g.41586463G>ACA8562732KRT14c.372C>T (p.Asp124=)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.41586463G>CCA399482523KRT14c.372C>G (p.Asp124Glu)
17g.41586463G=CA2260086832KRT14c.372C= (p.Asp124=)
17g.41586463G>TCA399482522KRT14c.372C>A (p.Asp124Glu)
ClinVar dbSNP gnomAD v4
17g.41586464T>ACA399482524KRT14c.371A>T (p.Asp124Val)
17g.41586464T>CCA399482528KRT14c.371A>G (p.Asp124Gly)
17g.41586464T>GCA399482526KRT14c.371A>C (p.Asp124Ala)
17g.41586465C>ACA399482529KRT14c.370G>T (p.Asp124Tyr)
17g.41586465C=CA2260086833KRT14c.370G= (p.Asp124=)
17g.41586465C>GCA399482531KRT14c.370G>C (p.Asp124His)
17g.41586465C>TCA8562733KRT14c.370G>A (p.Asp124Asn)
dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC
17g.41586466A=CA2260086834KRT14c.369T= (p.Asn123=)
17g.41586466A>CCA399482533KRT14c.369T>G (p.Asn123Lys)
17g.41586466A>GCA216915KRT14c.369T>C (p.Asn123=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.41586466A>TCA216913KRT14c.369T>A (p.Asn123Lys)
ClinVar dbSNP
17g.41586466_41586467delinsGCCA2739267536KRT14c.368_369delinsGC (p.Asn123Ser)
ClinVar
17g.41586467T>ACA399482536KRT14c.368A>T (p.Asn123Ile)
17g.41586467T>CCA216911KRT14c.368A>G (p.Asn123Ser)
ClinVar dbSNP
17g.41586467T>GCA399482537KRT14c.368A>C (p.Asn123Thr)
17g.41586467T=CA2260086835KRT14c.368A= (p.Asn123=)
17g.41586468T>ACA399482540KRT14c.367A>T (p.Asn123Tyr)
17g.41586468T>CCA399482541KRT14c.367A>G (p.Asn123Asp)
17g.41586468T>GCA399482542KRT14c.367A>C (p.Asn123His)
17g.41586469G>ACA499992002KRT14c.366C>T (p.Leu122=)
COSMIC
17g.41586469G>CCA499992003KRT14c.366C>G (p.Leu122=)
17g.41586469G>TCA499992004KRT14c.366C>A (p.Leu122=)
17g.41586470A>CCA399482545KRT14c.365T>G (p.Leu122Arg)
17g.41586470A>GCA399482548KRT14c.365T>C (p.Leu122Pro)
17g.41586470A>TCA399482546KRT14c.365T>A (p.Leu122His)
17g.41586471G>ACA216909KRT14c.364C>T (p.Leu122Phe)
ClinVar dbSNP gnomAD v4
17g.41586471G>CCA399482550KRT14c.364C>G (p.Leu122Val)
17g.41586471G=CA2260086836KRT14c.364C= (p.Leu122=)
17g.41586471G>TCA399482552KRT14c.364C>A (p.Leu122Ile)
17g.41586472G>ACA8562734KRT14c.363C>T (p.Asn121=)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.41586472G>CCA399482554KRT14c.363C>G (p.Asn121Lys)
17g.41586472G=CA2260086837KRT14c.363C= (p.Asn121=)
17g.41586472G>TCA399482556KRT14c.363C>A (p.Asn121Lys)
17g.41586473T>ACA399482558KRT14c.362A>T (p.Asn121Ile)
17g.41586473T>CCA399482560KRT14c.362A>G (p.Asn121Ser)
dbSNP gnomAD v4
17g.41586473T>GCA399482562KRT14c.362A>C (p.Asn121Thr)
17g.41586473T=CA2260086838KRT14c.362A= (p.Asn121=)
17g.41586474_41586480delCA2637837296KRT14c.356_362del (p.Met119ThrfsTer25)
gnomAD v4
17g.41586474T>ACA399482565KRT14c.361A>T (p.Asn121Tyr)
17g.41586474T>CCA399482567KRT14c.361A>G (p.Asn121Asp)
17g.41586474T>GCA399482564KRT14c.361A>C (p.Asn121His)
17g.41586475C>ACA399482569KRT14c.360G>T (p.Gln120His)
17g.41586475C>GCA399482571KRT14c.360G>C (p.Gln120His)
17g.41586475C>TCA499992006KRT14c.360G>A (p.Gln120=)
17g.41586476T>ACA399482573KRT14c.359A>T (p.Gln120Leu)
17g.41586476T>CCA216907KRT14c.359A>G (p.Gln120Arg)
ClinVar dbSNP
17g.41586476T>GCA216905KRT14c.359A>C (p.Gln120Pro)
ClinVar dbSNP
17g.41586476T=CA2260086839KRT14c.359A= (p.Gln120=)
17g.41586477G>ACA399482580KRT14c.358C>T (p.Gln120Ter)
17g.41586477G>CCA399482578KRT14c.358C>G (p.Gln120Glu)
17g.41586477G>TCA399482576KRT14c.358C>A (p.Gln120Lys)
17g.41586478C>ACA399482581KRT14c.357G>T (p.Met119Ile)
17g.41586478C=CA2260086840KRT14c.357G= (p.Met119=)
17g.41586478C>GCA399482582KRT14c.357G>C (p.Met119Ile)
17g.41586478C>TCA216903KRT14c.357G>A (p.Met119Ile)
ClinVar dbSNP
17g.41586479A=CA2260086841KRT14c.356T= (p.Met119=)
17g.41586479A>CCA399482585KRT14c.356T>G (p.Met119Arg)
ClinVar dbSNP
17g.41586479A>GCA216901KRT14c.356T>C (p.Met119Thr)
ClinVar dbSNP
17g.41586479A>TCA399482586KRT14c.356T>A (p.Met119Lys)
17g.41586480T>ACA399482589KRT14c.355A>T (p.Met119Leu)
17g.41586480T>CCA216899KRT14c.355A>G (p.Met119Val)
ClinVar dbSNP
17g.41586480T>GCA399482590KRT14c.355A>C (p.Met119Leu)
17g.41586480T=CA2260086842KRT14c.355A= (p.Met119=)
17g.41586481G>ACA499992007KRT14c.354C>T (p.Thr118=)
17g.41586481G>CCA499992008KRT14c.354C>G (p.Thr118=)
17g.41586481G=CA2260086843KRT14c.354C= (p.Thr118=)
17g.41586481G>TCA8562735KRT14c.354C>A (p.Thr118=)
dbSNP ExAC gnomAD v3 gnomAD v4
17g.41586482G>ACA16620405KRT14c.353C>T (p.Thr118Ile)
ClinVar dbSNP gnomAD v2 gnomAD v4
17g.41586482G>CCA399482594KRT14c.353C>G (p.Thr118Ser)
17g.41586482G=CA2260086844KRT14c.353C= (p.Thr118=)
17g.41586482G>TCA399482596KRT14c.353C>A (p.Thr118Asn)
dbSNP gnomAD v3 gnomAD v4
17g.41586483T>ACA399482599KRT14c.352A>T (p.Thr118Ser)
17g.41586483T>CCA399482600KRT14c.352A>G (p.Thr118Ala)
gnomAD v4
17g.41586483T>GCA399482601KRT14c.352A>C (p.Thr118Pro)
17g.41586484C>ACA8562736KRT14c.351G>T (p.Val117=)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.41586484C=CA2260086845KRT14c.351G= (p.Val117=)
17g.41586484C>GCA499992010KRT14c.351G>C (p.Val117=)
17g.41586484C>TCA499992009KRT14c.351G>A (p.Val117=)
gnomAD v4
17g.41586485A=CA2260086846KRT14c.350T= (p.Val117=)
17g.41586485A>CCA399482604KRT14c.350T>G (p.Val117Gly)
dbSNP
17g.41586485A>GCA399482605KRT14c.350T>C (p.Val117Ala)
dbSNP gnomAD v4
17g.41586485A>TCA399482607KRT14c.350T>A (p.Val117Glu)
17g.41586486C>ACA399482611KRT14c.349G>T (p.Val117Leu)
gnomAD v4
17g.41586486C>GCA399482610KRT14c.349G>C (p.Val117Leu)
17g.41586486C>TCA399482609KRT14c.349G>A (p.Val117Met)

Number of alleles fetched