Chr Mutation (hg38) CAid Gene Transcript Linkouts
17g.41586510_41586528delCA2809495446KRT14c.312_330del (p.Ala105TrpfsTer7)
17g.41586521_41586533delinsGCAAAGCCACCACCA2260086860KRT14c.302_314delinsGTGGTGGCTTTGC (p.Gly101=)
17g.41586535_41586546delCA8562745KRT14c.302_313del (p.Gly101_Phe104del)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.41586527C>ACA399482781KRT14c.308G>T (p.Gly103Val)
17g.41586527C=CA2260086865KRT14c.308G= (p.Gly103=)
17g.41586527C>GCA399482785KRT14c.308G>C (p.Gly103Ala)
17g.41586527C>TCA399482784KRT14c.308G>A (p.Gly103Asp)
dbSNP
17g.41586528C>ACA399482788KRT14c.307G>T (p.Gly103Cys)
17g.41586528C=CA2260086866KRT14c.307G= (p.Gly103=)
17g.41586528C>GCA399482790KRT14c.307G>C (p.Gly103Arg)
17g.41586528C>TCA8562749KRT14c.307G>A (p.Gly103Ser)
dbSNP ExAC gnomAD v2
17g.41586529A>CCA500205488KRT14c.306T>G (p.Gly102=)
17g.41586529A>GCA500205489KRT14c.306T>C (p.Gly102=)
17g.41586529A>TCA500205491KRT14c.306T>A (p.Gly102=)
17g.41586530C>ACA399482792KRT14c.305G>T (p.Gly102Val)
17g.41586530C=CA2260086867KRT14c.305G= (p.Gly102=)
17g.41586530C>GCA8562750KRT14c.305G>C (p.Gly102Ala)
dbSNP ExAC gnomAD v2 gnomAD v4
17g.41586530C>TCA399482794KRT14c.305G>A (p.Gly102Asp)
gnomAD v4
17g.41586531C>ACA399482795KRT14c.304G>T (p.Gly102Cys)
17g.41586531C=CA2260086868KRT14c.304G= (p.Gly102=)
17g.41586531C>GCA399482796KRT14c.304G>C (p.Gly102Arg)
dbSNP gnomAD v4
17g.41586531C>TCA399482797KRT14c.304G>A (p.Gly102Ser)
17g.41586532A=CA2260086869KRT14c.303T= (p.Gly101=)
17g.41586532A>CCA8562751KRT14c.303T>G (p.Gly101=)
dbSNP ExAC
17g.41586532A>GCA500205496KRT14c.303T>C (p.Gly101=)
17g.41586532A>TCA500205497KRT14c.303T>A (p.Gly101=)
17g.41586533C>ACA399482799KRT14c.302G>T (p.Gly101Val)
17g.41586533C=CA2260086870KRT14c.302G= (p.Gly101=)
17g.41586533C>GCA8562752KRT14c.302G>C (p.Gly101Ala)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.41586533C>TCA399482798KRT14c.302G>A (p.Gly101Asp)
17g.41586543_41586590dupCA983759153KRT14c.255_302dup (p.Gly101_Gly102insGlyGlyTyrGlyGlyGlyLeuGlyAlaGlyLeuGlyGlyGlyPheGly)
gnomAD v3 gnomAD v4
17g.41586534C>ACA399482800KRT14c.301G>T (p.Gly101Cys)
17g.41586534C>GCA399482801KRT14c.301G>C (p.Gly101Arg)
17g.41586534C>TCA399482802KRT14c.301G>A (p.Gly101Ser)
17g.41586535A=CA2260086871KRT14c.300T= (p.Phe100=)
17g.41586535A>CCA8562754KRT14c.300T>G (p.Phe100Leu)
dbSNP ExAC gnomAD v2 gnomAD v4
17g.41586535A>GCA500205499KRT14c.300T>C (p.Phe100=)
17g.41586535A>TCA399482803KRT14c.300T>A (p.Phe100Leu)
17g.41586535_41586547delinsAAAGCCACCACCCCA2260086872KRT14c.288_300delinsGGGTGGTGGCTTT (p.Leu96=)
17g.41586536A>CCA399482804KRT14c.299T>G (p.Phe100Cys)
17g.41586536A>GCA399482805KRT14c.299T>C (p.Phe100Ser)
17g.41586536A>TCA399482806KRT14c.299T>A (p.Phe100Tyr)
17g.41586542_41586553delCA8562753KRT14c.288_299del (p.Leu96_Gly99del)
dbSNP ExAC gnomAD v4
17g.41586537A>CCA399482807KRT14c.298T>G (p.Phe100Val)
17g.41586537A>GCA399482808KRT14c.298T>C (p.Phe100Leu)
17g.41586537A>TCA399482809KRT14c.298T>A (p.Phe100Ile)
17g.41586538G>ACA500205505KRT14c.297C>T (p.Gly99=)
dbSNP gnomAD v3 gnomAD v4
17g.41586538G>CCA500205506KRT14c.297C>G (p.Gly99=)
dbSNP gnomAD v3 gnomAD v4
17g.41586538G=CA2260086873KRT14c.297C= (p.Gly99=)
17g.41586538G>TCA500205507KRT14c.297C>A (p.Gly99=)
17g.41586539C>ACA399482811KRT14c.296G>T (p.Gly99Val)
17g.41586539C>GCA399482812KRT14c.296G>C (p.Gly99Ala)
17g.41586539C>TCA399482810KRT14c.296G>A (p.Gly99Asp)
17g.41586540_41586543delCA2637837315KRT14c.293_296del (p.Gly98AlafsTer19)
gnomAD v4
17g.41586540C>ACA399482815KRT14c.295G>T (p.Gly99Cys)
17g.41586540C=CA2260086874KRT14c.295G= (p.Gly99=)
17g.41586540C>GCA399482813KRT14c.295G>C (p.Gly99Arg)
17g.41586540C>TCA399482814KRT14c.295G>A (p.Gly99Ser)
dbSNP gnomAD v2 gnomAD v4
17g.41586541A=CA2260086875KRT14c.294T= (p.Gly98=)
17g.41586541A>CCA8562755KRT14c.294T>G (p.Gly98=)
dbSNP ExAC gnomAD v4
17g.41586541A>GCA500205512KRT14c.294T>C (p.Gly98=)
17g.41586541A>TCA500205511KRT14c.294T>A (p.Gly98=)
17g.41586542C>ACA399482816KRT14c.293G>T (p.Gly98Val)
COSMIC
17g.41586542C=CA2260086877KRT14c.293G= (p.Gly98=)
17g.41586542C>GCA399482817KRT14c.293G>C (p.Gly98Ala)
dbSNP gnomAD v2 gnomAD v4
17g.41586542C>TCA399482818KRT14c.293G>A (p.Gly98Asp)
dbSNP gnomAD v2 gnomAD v4
17g.41586542_41586554delinsCCACCCAAGCCAGCA2260086876KRT14c.281_293delinsCTGGCTTGGGTGG (p.Ala94=)
17g.41586543C>ACA399482819KRT14c.292G>T (p.Gly98Cys)
17g.41586543C>GCA399482820KRT14c.292G>C (p.Gly98Arg)
17g.41586543C>TCA399482821KRT14c.292G>A (p.Gly98Ser)
gnomAD v4
17g.41586547_41586558delCA772040919KRT14c.281_292del (p.Ala94_Gly97del)
dbSNP gnomAD v3 gnomAD v4
17g.41586544A=CA2260086878KRT14c.291T= (p.Gly97=)
17g.41586544A>CCA8562756KRT14c.291T>G (p.Gly97=)
dbSNP ExAC gnomAD v2 gnomAD v4
17g.41586544A>GCA500205515KRT14c.291T>C (p.Gly97=)
17g.41586544A>TCA500205516KRT14c.291T>A (p.Gly97=)
17g.41586545C>ACA399482822KRT14c.290G>T (p.Gly97Val)
17g.41586545C=CA2260086879KRT14c.290G= (p.Gly97=)
17g.41586545C>GCA399482823KRT14c.290G>C (p.Gly97Ala)
dbSNP
17g.41586545C>TCA399482824KRT14c.290G>A (p.Gly97Asp)
17g.41586546C>ACA399482827KRT14c.289G>T (p.Gly97Cys)
17g.41586546C>GCA399482825KRT14c.289G>C (p.Gly97Arg)
17g.41586546C>TCA399482826KRT14c.289G>A (p.Gly97Ser)
gnomAD v4
17g.41586547C>ACA8562757KRT14c.288G>T (p.Leu96Phe)
dbSNP ExAC gnomAD v2 gnomAD v4
17g.41586547C=CA2260086880KRT14c.288G= (p.Leu96=)
17g.41586547C>GCA8562758KRT14c.288G>C (p.Leu96Phe)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.41586547C>TCA500205519KRT14c.288G>A (p.Leu96=)
17g.41586548A>CCA399482828KRT14c.287T>G (p.Leu96Trp)
17g.41586548A>GCA399482829KRT14c.287T>C (p.Leu96Ser)
17g.41586548A>TCA399482830KRT14c.287T>A (p.Leu96Ter)
17g.41586553_41586554insCCACCGAAGCCACA8562759KRT14c.287_288insCGGTGGTGGCTT (p.Gly95_Leu96insPheGlyGlyGly)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.41586549A>CCA399482831KRT14c.286T>G (p.Leu96Val)
17g.41586549A>GCA500205521KRT14c.286T>C (p.Leu96=)
17g.41586549A>TCA399482832KRT14c.286T>A (p.Leu96Met)
17g.41586550G>ACA500205522KRT14c.285C>T (p.Gly95=)
gnomAD v4
17g.41586550G>CCA500205524KRT14c.285C>G (p.Gly95=)
gnomAD v4
17g.41586550G>TCA500205523KRT14c.285C>A (p.Gly95=)
17g.41586551C>ACA399482833KRT14c.284G>T (p.Gly95Val)
17g.41586551C>GCA399482834KRT14c.284G>C (p.Gly95Ala)
17g.41586551C>TCA399482835KRT14c.284G>A (p.Gly95Asp)
gnomAD v4
17g.41586552C>ACA399482838KRT14c.283G>T (p.Gly95Cys)
17g.41586552C>GCA399482837KRT14c.283G>C (p.Gly95Arg)
17g.41586552C>TCA399482836KRT14c.283G>A (p.Gly95Ser)
COSMIC
17g.41586553A=CA2260086881KRT14c.282T= (p.Ala94=)
17g.41586553A>CCA500205530KRT14c.282T>G (p.Ala94=)
17g.41586553A>GCA500205529KRT14c.282T>C (p.Ala94=)
17g.41586553A>TCA8562760KRT14c.282T>A (p.Ala94=)
dbSNP ExAC gnomAD v2 gnomAD v4
17g.41586554G>ACA8562761KRT14c.281C>T (p.Ala94Val)
dbSNP ExAC gnomAD v2 gnomAD v4
17g.41586554G>CCA399482839KRT14c.281C>G (p.Ala94Gly)
dbSNP gnomAD v4
17g.41586554G=CA2260086882KRT14c.281C= (p.Ala94=)
17g.41586554G>TCA399482840KRT14c.281C>A (p.Ala94Asp)
17g.41586555C>ACA399482841KRT14c.280G>T (p.Ala94Ser)
17g.41586555C=CA2260086883KRT14c.280G= (p.Ala94=)
17g.41586555C>GCA399482842KRT14c.280G>C (p.Ala94Pro)
17g.41586555C>TCA216890KRT14c.280G>A (p.Ala94Thr)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.41586556A>CCA500205532KRT14c.279T>G (p.Gly93=)
17g.41586556A>GCA500205533KRT14c.279T>C (p.Gly93=)
17g.41586556A>TCA500205534KRT14c.279T>A (p.Gly93=)
17g.41586557C>ACA399482843KRT14c.278G>T (p.Gly93Val)
17g.41586557C=CA2260086884KRT14c.278G= (p.Gly93=)
17g.41586557C>GCA399482844KRT14c.278G>C (p.Gly93Ala)
17g.41586557C>TCA399482845KRT14c.278G>A (p.Gly93Asp)
dbSNP gnomAD v4
17g.41586558C>ACA399482846KRT14c.277G>T (p.Gly93Cys)
gnomAD v4
17g.41586558C>GCA399482847KRT14c.277G>C (p.Gly93Arg)
17g.41586558C>TCA399482848KRT14c.277G>A (p.Gly93Ser)
17g.41586559A>CCA500205536KRT14c.276T>G (p.Leu92=)
17g.41586559A>GCA500205537KRT14c.276T>C (p.Leu92=)
gnomAD v4
17g.41586559A>TCA500205538KRT14c.276T>A (p.Leu92=)
17g.41586560A>CCA399482851KRT14c.275T>G (p.Leu92Arg)
17g.41586560A>GCA399482849KRT14c.275T>C (p.Leu92Pro)
17g.41586560A>TCA399482850KRT14c.275T>A (p.Leu92His)
17g.41586561G>ACA399482852KRT14c.274C>T (p.Leu92Phe)
17g.41586561G>CCA399482853KRT14c.274C>G (p.Leu92Val)
17g.41586561G>TCA399482854KRT14c.274C>A (p.Leu92Ile)
17g.41586562G>ACA500205540KRT14c.273C>T (p.Gly91=)
gnomAD v4
17g.41586562G>CCA500205542KRT14c.273C>G (p.Gly91=)
17g.41586562G>TCA500205541KRT14c.273C>A (p.Gly91=)
17g.41586563C>ACA399482855KRT14c.272G>T (p.Gly91Val)
17g.41586563C=CA2260086885KRT14c.272G= (p.Gly91=)
17g.41586563C>GCA399482856KRT14c.272G>C (p.Gly91Ala)
17g.41586563C>TCA399482857KRT14c.272G>A (p.Gly91Asp)
dbSNP gnomAD v3 gnomAD v4
17g.41586564C>ACA399482858KRT14c.271G>T (p.Gly91Cys)
17g.41586564C>GCA399482859KRT14c.271G>C (p.Gly91Arg)
17g.41586564C>TCA399482860KRT14c.271G>A (p.Gly91Ser)
17g.41586565A>CCA500205544KRT14c.270T>G (p.Gly90=)
17g.41586565A>GCA500205545KRT14c.270T>C (p.Gly90=)
17g.41586565A>TCA500205546KRT14c.270T>A (p.Gly90=)
17g.41586566C>ACA399482861KRT14c.269G>T (p.Gly90Val)
17g.41586566C>GCA399482862KRT14c.269G>C (p.Gly90Ala)
17g.41586566C>TCA399482863KRT14c.269G>A (p.Gly90Asp)
17g.41586567C>ACA290665637KRT14c.268G>T (p.Gly90Cys)
dbSNP
17g.41586567C=CA2260086886KRT14c.268G= (p.Gly90=)
17g.41586567C>GCA399482865KRT14c.268G>C (p.Gly90Arg)
17g.41586567C>TCA399482864KRT14c.268G>A (p.Gly90Ser)
17g.41586568A=CA2260086887KRT14c.267T= (p.Gly89=)
17g.41586568A>CCA500205549KRT14c.267T>G (p.Gly89=)
17g.41586568A>GCA500205550KRT14c.267T>C (p.Gly89=)
dbSNP gnomAD v2 gnomAD v4
17g.41586568A>TCA500205551KRT14c.267T>A (p.Gly89=)
17g.41586569C>ACA399482867KRT14c.266G>T (p.Gly89Val)
17g.41586569C=CA2260086888KRT14c.266G= (p.Gly89=)
17g.41586569C>GCA8562762KRT14c.266G>C (p.Gly89Ala)
dbSNP ExAC gnomAD v2 gnomAD v4
17g.41586569C>TCA399482866KRT14c.266G>A (p.Gly89Asp)
dbSNP gnomAD v3 gnomAD v4
17g.41586570C>ACA399482868KRT14c.265G>T (p.Gly89Cys)
17g.41586570C=CA2260086889KRT14c.265G= (p.Gly89=)
17g.41586570C>GCA399482869KRT14c.265G>C (p.Gly89Arg)
17g.41586570C>TCA399482870KRT14c.265G>A (p.Gly89Ser)
dbSNP gnomAD v2 gnomAD v4
17g.41586571A=CA2260086890KRT14c.264T= (p.Tyr88=)
17g.41586571A>CCA399482872KRT14c.264T>G (p.Tyr88Ter)
17g.41586571A>GCA8562763KRT14c.264T>C (p.Tyr88=)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.41586571A>TCA399482871KRT14c.264T>A (p.Tyr88Ter)
17g.41586572T>ACA399482873KRT14c.263A>T (p.Tyr88Phe)
17g.41586572T>CCA399482874KRT14c.263A>G (p.Tyr88Cys)
17g.41586572T>GCA399482875KRT14c.263A>C (p.Tyr88Ser)
17g.41586572_41586573delinsTACA2260086891KRT14c.262_263delinsTA (p.Tyr88=)
17g.41586573delCA2260086892KRT14c.262del (p.Tyr88MetfsTer30)
dbSNP
17g.41586573A>CCA399482876KRT14c.262T>G (p.Tyr88Asp)
17g.41586573A>GCA399482877KRT14c.262T>C (p.Tyr88His)
17g.41586573A>TCA399482878KRT14c.262T>A (p.Tyr88Asn)
17g.41586574T>ACA500205558KRT14c.261A>T (p.Gly87=)
dbSNP gnomAD v3 gnomAD v4
17g.41586574T>CCA500205561KRT14c.261A>G (p.Gly87=)
17g.41586574T>GCA500205559KRT14c.261A>C (p.Gly87=)
17g.41586574T=CA2260086893KRT14c.261A= (p.Gly87=)
17g.41586575C>ACA399482881KRT14c.260G>T (p.Gly87Val)
17g.41586575C>GCA399482879KRT14c.260G>C (p.Gly87Ala)
17g.41586575C>TCA399482880KRT14c.260G>A (p.Gly87Glu)
gnomAD v4
17g.41586576C>ACA399482882KRT14c.259G>T (p.Gly87Ter)
17g.41586576C>GCA399482883KRT14c.259G>C (p.Gly87Arg)
17g.41586576C>TCA399482884KRT14c.259G>A (p.Gly87Arg)
17g.41586577T>ACA500205565KRT14c.258A>T (p.Gly86=)
17g.41586577T>CCA8562764KRT14c.258A>G (p.Gly86=)
dbSNP ExAC gnomAD v2 gnomAD v4
17g.41586577T>GCA500205563KRT14c.258A>C (p.Gly86=)
17g.41586577T=CA2260086895KRT14c.258A= (p.Gly86=)
17g.41586577_41586578delinsTCCA2260086894KRT14c.257_258delinsGA (p.Gly86=)
17g.41586578C>ACA399482885KRT14c.257G>T (p.Gly86Val)
17g.41586578C=CA2260086897KRT14c.257G= (p.Gly86=)
17g.41586578C>GCA399482886KRT14c.257G>C (p.Gly86Ala)
dbSNP gnomAD v3 gnomAD v4
17g.41586578C>TCA399482887KRT14c.257G>A (p.Gly86Glu)
17g.41586582dupCA2260086896KRT14c.257dup (p.Gly87ArgfsTer22)
dbSNP
17g.41586582delCA645584615KRT14c.257del (p.Gly86GlufsTer?)
dbSNP COSMIC
17g.41586579C>ACA399482888KRT14c.256G>T (p.Gly86Ter)
17g.41586579C>GCA399482889KRT14c.256G>C (p.Gly86Arg)
17g.41586579C>TCA399482890KRT14c.256G>A (p.Gly86Arg)
17g.41586580C>ACA500205573KRT14c.255G>T (p.Gly85=)
17g.41586580C>GCA500205574KRT14c.255G>C (p.Gly85=)
17g.41586580C>TCA500205575KRT14c.255G>A (p.Gly85=)
gnomAD v4
17g.41586581C>ACA399482891KRT14c.254G>T (p.Gly85Val)
17g.41586581C=CA2260086898KRT14c.254G= (p.Gly85=)
17g.41586581C>GCA399482892KRT14c.254G>C (p.Gly85Ala)
dbSNP gnomAD v4
17g.41586581C>TCA399482893KRT14c.254G>A (p.Gly85Glu)
17g.41586582C>ACA399482894KRT14c.253G>T (p.Gly85Trp)
dbSNP gnomAD v4
17g.41586582C=CA2260086899KRT14c.253G= (p.Gly85=)
17g.41586582C>GCA399482896KRT14c.253G>C (p.Gly85Arg)
17g.41586582C>TCA399482895KRT14c.253G>A (p.Gly85Arg)
dbSNP gnomAD v3 gnomAD v4
17g.41586583A=CA2260086900KRT14c.252T= (p.Phe84=)
17g.41586583A>CCA399482897KRT14c.252T>G (p.Phe84Leu)
17g.41586583A>GCA8562765KRT14c.252T>C (p.Phe84=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.41586583A>TCA399482898KRT14c.252T>A (p.Phe84Leu)
17g.41586584A>CCA399482899KRT14c.251T>G (p.Phe84Cys)
gnomAD v4
17g.41586584A>GCA399482900KRT14c.251T>C (p.Phe84Ser)
17g.41586584A>TCA399482901KRT14c.251T>A (p.Phe84Tyr)
17g.41586585A>CCA399482902KRT14c.250T>G (p.Phe84Val)
17g.41586585A>GCA399482903KRT14c.250T>C (p.Phe84Leu)
17g.41586585A>TCA399482904KRT14c.250T>A (p.Phe84Ile)
17g.41586585_41586586insACACA2809495458KRT14c.250_251insGTT (p.Gly83_Phe84insCys)
17g.41586586delCA2637837383KRT14c.249del (p.Phe84LeufsTer?)
gnomAD v4
17g.41586586G>ACA500205581KRT14c.249C>T (p.Gly83=)
17g.41586586G>CCA500205583KRT14c.249C>G (p.Gly83=)
17g.41586586G>TCA500205584KRT14c.249C>A (p.Gly83=)
17g.41586587C>ACA399482905KRT14c.248G>T (p.Gly83Val)
17g.41586587C=CA2260086901KRT14c.248G= (p.Gly83=)
17g.41586587C>GCA8562766KRT14c.248G>C (p.Gly83Ala)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.41586587C>TCA399482906KRT14c.248G>A (p.Gly83Asp)
17g.41586588C>ACA399482908KRT14c.247G>T (p.Gly83Cys)
17g.41586588C=CA2260086902KRT14c.247G= (p.Gly83=)
17g.41586588C>GCA399482907KRT14c.247G>C (p.Gly83Arg)
17g.41586588C>TCA8562767KRT14c.247G>A (p.Gly83Ser)
dbSNP ExAC gnomAD v2 gnomAD v4
17g.41586589A=CA2260086903KRT14c.246T= (p.Ser82=)
17g.41586589A>CCA399482909KRT14c.246T>G (p.Ser82Arg)
17g.41586589A>GCA500205592KRT14c.246T>C (p.Ser82=)
17g.41586589A>TCA399482910KRT14c.246T>A (p.Ser82Arg)
dbSNP gnomAD v4
17g.41586589_41586590insACACACCCA2809495464KRT14c.245_246insGGTGTGT (p.Ser82ArgfsTer29)
17g.41586590C>ACA399482911KRT14c.245G>T (p.Ser82Ile)
17g.41586590C>GCA399482912KRT14c.245G>C (p.Ser82Thr)
17g.41586590C>TCA399482913KRT14c.245G>A (p.Ser82Asn)
17g.41586590_41586591delCA2809495465KRT14c.244_245del (p.Ser82TrpfsTer26)
17g.41586591T>ACA399482914KRT14c.244A>T (p.Ser82Cys)
17g.41586591T>CCA399482915KRT14c.244A>G (p.Ser82Gly)
17g.41586591T>GCA399482916KRT14c.244A>C (p.Ser82Arg)
17g.41586592A=CA2260086904KRT14c.243T= (p.Gly81=)
17g.41586592A>CCA500205598KRT14c.243T>G (p.Gly81=)
17g.41586592A>GCA500205600KRT14c.243T>C (p.Gly81=)
17g.41586592A>TCA500205601KRT14c.243T>A (p.Gly81=)
gnomAD v4
17g.41586592_41586593dupCA2741535162KRT14c.242_243dup (p.Ser82ValfsTer?)
17g.41586593C>ACA399482917KRT14c.242G>T (p.Gly81Val)
gnomAD v4
17g.41586593C>GCA399482918KRT14c.242G>C (p.Gly81Ala)
COSMIC
17g.41586593C>TCA399482919KRT14c.242G>A (p.Gly81Asp)
17g.41586594dupCA216889KRT14c.242dup (p.Ser82Ter)
ClinVar dbSNP
17g.41586594C>ACA399482922KRT14c.241G>T (p.Gly81Cys)
dbSNP gnomAD v3 gnomAD v4
17g.41586594C=CA2260086905KRT14c.241G= (p.Gly81=)
17g.41586594C>GCA399482921KRT14c.241G>C (p.Gly81Arg)
17g.41586594C>TCA399482920KRT14c.241G>A (p.Gly81Ser)
17g.41586595A=CA2260086906KRT14c.240T= (p.Phe80=)
17g.41586595A>CCA399482923KRT14c.240T>G (p.Phe80Leu)
17g.41586595A>GCA290665638KRT14c.240T>C (p.Phe80=)
dbSNP
17g.41586595A>TCA399482924KRT14c.240T>A (p.Phe80Leu)
17g.41586596A>CCA399482925KRT14c.239T>G (p.Phe80Cys)
17g.41586596A>GCA399482926KRT14c.239T>C (p.Phe80Ser)
17g.41586596A>TCA399482927KRT14c.239T>A (p.Phe80Tyr)
17g.41586597A>CCA399482928KRT14c.238T>G (p.Phe80Val)
17g.41586597A>GCA399482929KRT14c.238T>C (p.Phe80Leu)
17g.41586597A>TCA399482930KRT14c.238T>A (p.Phe80Ile)
17g.41586597_41586603delinsAGCTGCTCA2260086907KRT14c.232_238delinsAGCAGCT (p.Ser78=)
17g.41586598G>ACA500205612KRT14c.237C>T (p.Ser79=)
17g.41586598G>CCA399482931KRT14c.237C>G (p.Ser79Arg)
17g.41586598G>TCA399482932KRT14c.237C>A (p.Ser79Arg)
17g.41586614_41586616dupCA8562770KRT14c.235_237dup (p.Ser79_Phe80insSer)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.41586611_41586616dupCA919841702KRT14c.232_237dup (p.Ser79_Phe80insSerSer)
dbSNP
17g.41586608_41586616dupCA2733646329KRT14c.229_237dup (p.Ser79_Phe80insSerSerSer)
dbSNP
17g.41586614_41586616delCA8562768KRT14c.235_237del (p.Ser79del)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
17g.41586611_41586616delCA8562769KRT14c.232_237del (p.Ser78_Ser79del)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
17g.41586599C>ACA399482934KRT14c.236G>T (p.Ser79Ile)
17g.41586599C=CA2260086908KRT14c.236G= (p.Ser79=)
17g.41586599C>GCA399482933KRT14c.236G>C (p.Ser79Thr)
17g.41586599C>TCA8562771KRT14c.236G>A (p.Ser79Asn)
dbSNP ExAC gnomAD v2 gnomAD v4
17g.41586600delCA500205622KRT14c.235del (p.Ser79AlafsTer?)
COSMIC
17g.41586600T>ACA399482935KRT14c.235A>T (p.Ser79Cys)
gnomAD v4
17g.41586600T>CCA399482936KRT14c.235A>G (p.Ser79Gly)
dbSNP
17g.41586600T>GCA399482937KRT14c.235A>C (p.Ser79Arg)
17g.41586600T=CA2260086909KRT14c.235A= (p.Ser79=)
17g.41586601G>ACA290665641KRT14c.234C>T (p.Ser78=)
dbSNP
17g.41586601G>CCA399482938KRT14c.234C>G (p.Ser78Arg)
17g.41586601G=CA2260086910KRT14c.234C= (p.Ser78=)
17g.41586601G>TCA399482939KRT14c.234C>A (p.Ser78Arg)
gnomAD v4
17g.41586602C>ACA399482940KRT14c.233G>T (p.Ser78Ile)
17g.41586602C=CA2260086911KRT14c.233G= (p.Ser78=)
17g.41586602C>GCA399482941KRT14c.233G>C (p.Ser78Thr)
dbSNP gnomAD v2 gnomAD v4
17g.41586602C>TCA399482942KRT14c.233G>A (p.Ser78Asn)
17g.41586603T>ACA399482943KRT14c.232A>T (p.Ser78Cys)
17g.41586603T>CCA399482944KRT14c.232A>G (p.Ser78Gly)
17g.41586603T>GCA399482945KRT14c.232A>C (p.Ser78Arg)
17g.41586604G>ACA216887KRT14c.231C>T (p.Ser77=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.41586604G>CCA399482947KRT14c.231C>G (p.Ser77Arg)
17g.41586604G=CA2260086912KRT14c.231C= (p.Ser77=)
17g.41586604G>TCA399482946KRT14c.231C>A (p.Ser77Arg)
17g.41586605C>ACA399482948KRT14c.230G>T (p.Ser77Ile)
17g.41586605C>GCA399482949KRT14c.230G>C (p.Ser77Thr)
17g.41586605C>TCA399482950KRT14c.230G>A (p.Ser77Asn)
17g.41586606T>ACA399482951KRT14c.229A>T (p.Ser77Cys)
17g.41586606T>CCA399482952KRT14c.229A>G (p.Ser77Gly)
17g.41586606T>GCA399482953KRT14c.229A>C (p.Ser77Arg)
17g.41586607G>ACA500205636KRT14c.228C>T (p.Ser76=)
17g.41586607G>CCA399482954KRT14c.228C>G (p.Ser76Arg)
17g.41586607G>TCA399482955KRT14c.228C>A (p.Ser76Arg)
17g.41586608C>ACA399482956KRT14c.227G>T (p.Ser76Ile)
17g.41586608C=CA2260086913KRT14c.227G= (p.Ser76=)
17g.41586608C>GCA399482957KRT14c.227G>C (p.Ser76Thr)
17g.41586608C>TCA399482958KRT14c.227G>A (p.Ser76Asn)
dbSNP gnomAD v2
17g.41586608_41586609insCTCCA2809495469KRT14c.227_228insAGG (p.Ser76delinsArgGly)
17g.41586609T>ACA399482959KRT14c.226A>T (p.Ser76Cys)
17g.41586609T>CCA399482960KRT14c.226A>G (p.Ser76Gly)
17g.41586609T>GCA399482961KRT14c.226A>C (p.Ser76Arg)
17g.41586610G>ACA500205642KRT14c.225C>T (p.Ser75=)
17g.41586610G>CCA399482962KRT14c.225C>G (p.Ser75Arg)
17g.41586610G>TCA399482963KRT14c.225C>A (p.Ser75Arg)
17g.41586610_41586611delinsGCCA2260086914KRT14c.224_225delinsGC (p.Ser75=)
17g.41586611delCA626215416KRT14c.224del (p.Ser75ThrfsTer?)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
17g.41586611C>ACA399482964KRT14c.224G>T (p.Ser75Ile)
17g.41586611C>GCA399482965KRT14c.224G>C (p.Ser75Thr)
17g.41586611C>TCA399482966KRT14c.224G>A (p.Ser75Asn)
COSMIC
17g.41586612T>ACA399482967KRT14c.223A>T (p.Ser75Cys)
17g.41586612T>CCA8562772KRT14c.223A>G (p.Ser75Gly)
dbSNP ExAC gnomAD v2 gnomAD v4
17g.41586612T>GCA399482968KRT14c.223A>C (p.Ser75Arg)
17g.41586612T=CA2260086915KRT14c.223A= (p.Ser75=)
17g.41586613G>ACA8562773KRT14c.222C>T (p.Ser74=)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.41586613G>CCA399482969KRT14c.222C>G (p.Ser74Arg)
17g.41586613G=CA2260086916KRT14c.222C= (p.Ser74=)
17g.41586613G>TCA399482970KRT14c.222C>A (p.Ser74Arg)
17g.41586614C>ACA399482971KRT14c.221G>T (p.Ser74Ile)
17g.41586614C=CA2260086917KRT14c.221G= (p.Ser74=)
17g.41586614C>GCA399482972KRT14c.221G>C (p.Ser74Thr)
17g.41586614C>TCA8562774KRT14c.221G>A (p.Ser74Asn)
dbSNP ExAC gnomAD v2 gnomAD v4
17g.41586615T>ACA399482973KRT14c.220A>T (p.Ser74Cys)
17g.41586615T>CCA399482975KRT14c.220A>G (p.Ser74Gly)
gnomAD v4
17g.41586615T>GCA399482974KRT14c.220A>C (p.Ser74Arg)
17g.41586616G>ACA8562775KRT14c.219C>T (p.Phe73=)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.41586616G>CCA399482977KRT14c.219C>G (p.Phe73Leu)
17g.41586616G=CA2260086918KRT14c.219C= (p.Phe73=)
17g.41586616G>TCA399482976KRT14c.219C>A (p.Phe73Leu)
17g.41586617A>CCA399482978KRT14c.218T>G (p.Phe73Cys)
17g.41586617A>GCA399482980KRT14c.218T>C (p.Phe73Ser)
17g.41586617A>TCA399482979KRT14c.218T>A (p.Phe73Tyr)
COSMIC
17g.41586618A>CCA399482981KRT14c.217T>G (p.Phe73Val)
17g.41586618A>GCA399482982KRT14c.217T>C (p.Phe73Leu)
17g.41586618A>TCA399482983KRT14c.217T>A (p.Phe73Ile)
17g.41586619G>ACA500205645KRT14c.216C>T (p.Gly72=)
gnomAD v4
17g.41586619G>CCA500205646KRT14c.216C>G (p.Gly72=)
17g.41586619G>TCA500205649KRT14c.216C>A (p.Gly72=)
17g.41586620C>ACA8562776KRT14c.215G>T (p.Gly72Val)
dbSNP ExAC gnomAD v4
17g.41586620C=CA2260086919KRT14c.215G= (p.Gly72=)
17g.41586620C>GCA399482984KRT14c.215G>C (p.Gly72Ala)
17g.41586620C>TCA8562777KRT14c.215G>A (p.Gly72Asp)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.41586621C>ACA399482985KRT14c.214G>T (p.Gly72Cys)
gnomAD v4
17g.41586621C=CA2260086920KRT14c.214G= (p.Gly72=)
17g.41586621C>GCA399482986KRT14c.214G>C (p.Gly72Arg)
17g.41586621C>TCA290665647KRT14c.214G>A (p.Gly72Ser)
dbSNP gnomAD v4
17g.41586622A=CA2260086921KRT14c.213T= (p.Gly71=)
17g.41586622A>CCA500205650KRT14c.213T>G (p.Gly71=)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
17g.41586622A>GCA8562778KRT14c.213T>C (p.Gly71=)
dbSNP ExAC gnomAD v2 gnomAD v4
17g.41586622A>TCA500205651KRT14c.213T>A (p.Gly71=)
17g.41586623C>ACA399482988KRT14c.212G>T (p.Gly71Val)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
17g.41586623C=CA2260086922KRT14c.212G= (p.Gly71=)
17g.41586623C>GCA399482990KRT14c.212G>C (p.Gly71Ala)
17g.41586623C>TCA8562779KRT14c.212G>A (p.Gly71Asp)
dbSNP ExAC
17g.41586624C>ACA399482992KRT14c.211G>T (p.Gly71Cys)
17g.41586624C=CA2260086923KRT14c.211G= (p.Gly71=)
17g.41586624C>GCA399482993KRT14c.211G>C (p.Gly71Arg)
gnomAD v4
17g.41586624C>TCA8562780KRT14c.211G>A (p.Gly71Ser)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.41586625G>ACA8562781KRT14c.210C>T (p.Gly70=)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.41586625G>CCA500205659KRT14c.210C>G (p.Gly70=)
17g.41586625G=CA2260086924KRT14c.210C= (p.Gly70=)
17g.41586625G>TCA8562782KRT14c.210C>A (p.Gly70=)
dbSNP ExAC gnomAD v2 gnomAD v4
17g.41586626C>ACA399482994KRT14c.209G>T (p.Gly70Val)
gnomAD v4
17g.41586626C>GCA399482995KRT14c.209G>C (p.Gly70Ala)
17g.41586626C>TCA399482996KRT14c.209G>A (p.Gly70Asp)
17g.41586627C>ACA399482997KRT14c.208G>T (p.Gly70Cys)
dbSNP gnomAD v2
17g.41586627C=CA2260086925KRT14c.208G= (p.Gly70=)
17g.41586627C>GCA399482998KRT14c.208G>C (p.Gly70Arg)
17g.41586627C>TCA399482999KRT14c.208G>A (p.Gly70Ser)

Number of alleles fetched