Chr Mutation (hg38) CAid Gene Transcript Linkouts
17g.41586287_41586313delCA2637837224KRT14c.524_525+25del
gnomAD v4
17g.41586286G>ACA2637837225KRT14c.525+24C>T (n.525+24C>T)
gnomAD v4
17g.41586287C=CA2260086751KRT14c.525+23G= (n.525+23G=)
17g.41586287C>GCA2637837226KRT14c.525+23G>C (n.525+23G>C)
gnomAD v4
17g.41586287C>TCA8562700KRT14c.525+23G>A (n.525+23G>A)
dbSNP ExAC gnomAD v2 gnomAD v4
17g.41586288delCA656360527KRT14c.525+23del (n.525+23del)
COSMIC
17g.41586291C>GCA2637837228KRT14c.525+19G>C (n.525+19G>C)
gnomAD v4
17g.41586295_41586297delCA2637837227KRT14c.525+17_525+19del (n.525+17_525+19del)
gnomAD v4
17g.41586292T>CCA2260086753KRT14c.525+18A>G (n.525+18A>G)
dbSNP
17g.41586292T=CA2260086752KRT14c.525+18A= (n.525+18A=)
17g.41586293G>ACA290665523KRT14c.525+17C>T (n.525+17C>T)
dbSNP
17g.41586293G>CCA772040557KRT14c.525+17C>G (n.525+17C>G)
dbSNP gnomAD v3 gnomAD v4
17g.41586293G=CA2260086754KRT14c.525+17C= (n.525+17C=)
17g.41586294C>ACA2637837229KRT14c.525+16G>T (n.525+16G>T)
gnomAD v4
17g.41586296G>ACA2576267788KRT14c.525+14C>T (n.525+14C>T)
17g.41586296G=CA2260086755KRT14c.525+14C= (n.525+14C=)
17g.41586296G>TCA626215571KRT14c.525+14C>A (n.525+14C>A)
dbSNP gnomAD v2 gnomAD v4
17g.41586297C>TCA2809495427KRT14c.525+13G>A (n.525+13G>A)
17g.41586298C=CA2260086756KRT14c.525+12G= (n.525+12G=)
17g.41586298C>TCA290665525KRT14c.525+12G>A (n.525+12G>A)
dbSNP gnomAD v4
17g.41586300A=CA2260086757KRT14c.525+10T= (n.525+10T=)
17g.41586300A>TCA8562701KRT14c.525+10T>A (n.525+10T>A)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.41586301T>GCA2637837230KRT14c.525+9A>C (n.525+9A>C)
gnomAD v4
17g.41586303C=CA2260086758KRT14c.525+7G= (n.525+7G=)
17g.41586303C>TCA8562702KRT14c.525+7G>A (n.525+7G>A)
dbSNP ExAC gnomAD v2 gnomAD v4
17g.41586305C>GCA2637837231KRT14c.525+5G>C (n.525+5G>C)
gnomAD v4
17g.41586307delCA2637837232KRT14c.525+5del (n.525+5del)
gnomAD v4
17g.41586306C=CA2260086759KRT14c.525+4G= (n.525+4G=)
17g.41586306C>TCA772040561KRT14c.525+4G>A (n.525+4G>A)
dbSNP gnomAD v4
17g.41586307C>ACA290665529KRT14c.525+3G>T (n.525+3G>T)
dbSNP
17g.41586307C=CA2260086760KRT14c.525+3G= (n.525+3G=)
17g.41586307C>GCA290665531KRT14c.525+3G>C (n.525+3G>C)
dbSNP
17g.41586308A>CCA399481620KRT14c.525+2T>G (n.525+2T>G)
17g.41586308A>GCA399481626KRT14c.525+2T>C (n.525+2T>C)
17g.41586308A>TCA399481623KRT14c.525+2T>A (n.525+2T>A)
17g.41586309C>ACA399481629KRT14c.525+1G>T (n.525+1G>T)
gnomAD v4
17g.41586309C=CA2260086761KRT14c.525+1G= (n.525+1G=)
17g.41586309C>GCA290665533KRT14c.525+1G>C (n.525+1G>C)
dbSNP
17g.41586309C>TCA290665535KRT14c.525+1G>A (n.525+1G>A)
dbSNP COSMIC
17g.41586310C>ACA399481635KRT14c.525G>T (p.Lys175Asn)
17g.41586310C=CA2260086762KRT14c.525G= (p.Lys175=)
17g.41586310C>GCA399481636KRT14c.525G>C (p.Lys175Asn)
gnomAD v4
17g.41586310C>TCA8562703KRT14c.525G>A (p.Lys175=)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.41586311T>ACA399481640KRT14c.524A>T (p.Lys175Met)
dbSNP
17g.41586311T>CCA399481643KRT14c.524A>G (p.Lys175Arg)
gnomAD v4
17g.41586311T>GCA399481646KRT14c.524A>C (p.Lys175Thr)
17g.41586311T=CA2260086763KRT14c.524A= (p.Lys175=)
17g.41586312T>ACA399481649KRT14c.523A>T (p.Lys175Ter)
17g.41586312T>CCA399481650KRT14c.523A>G (p.Lys175Glu)
gnomAD v4
17g.41586312T>GCA399481653KRT14c.523A>C (p.Lys175Gln)
17g.41586313G>ACA499991545KRT14c.522C>T (p.Asn174=)
gnomAD v4
17g.41586313G>CCA399481664KRT14c.522C>G (p.Asn174Lys)
17g.41586313G>TCA399481666KRT14c.522C>A (p.Asn174Lys)
17g.41586314T>ACA399481670KRT14c.521A>T (p.Asn174Ile)
17g.41586314T>CCA399481672KRT14c.521A>G (p.Asn174Ser)
gnomAD v4
17g.41586314T>GCA399481674KRT14c.521A>C (p.Asn174Thr)
17g.41586315T>ACA399481677KRT14c.520A>T (p.Asn174Tyr)
17g.41586315T>CCA399481680KRT14c.520A>G (p.Asn174Asp)
17g.41586315T>GCA399481683KRT14c.520A>C (p.Asn174His)
17g.41586316C>ACA399481684KRT14c.519G>T (p.Arg173Ser)
17g.41586316C>GCA399481689KRT14c.519G>C (p.Arg173Ser)
17g.41586316C>TCA499991564KRT14c.519G>A (p.Arg173=)
17g.41586317C>ACA8562704KRT14c.518G>T (p.Arg173Met)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
17g.41586317C=CA2260086764KRT14c.518G= (p.Arg173=)
17g.41586317C>GCA399481695KRT14c.518G>C (p.Arg173Thr)
17g.41586317C>TCA399481697KRT14c.518G>A (p.Arg173Lys)
17g.41586318T>ACA399481702KRT14c.517A>T (p.Arg173Trp)
17g.41586318T>CCA399481703KRT14c.517A>G (p.Arg173Gly)
17g.41586318T>GCA499991573KRT14c.517A>C (p.Arg173=)
17g.41586319C>ACA499991574KRT14c.516G>T (p.Leu172=)
17g.41586319C=CA2260086765KRT14c.516G= (p.Leu172=)
17g.41586319C>GCA499991576KRT14c.516G>C (p.Leu172=)
dbSNP gnomAD v4
17g.41586319C>TCA499991575KRT14c.516G>A (p.Leu172=)
COSMIC
17g.41586320A>CCA399481705KRT14c.515T>G (p.Leu172Arg)
17g.41586320A>GCA399481709KRT14c.515T>C (p.Leu172Pro)
gnomAD v4
17g.41586320A>TCA399481707KRT14c.515T>A (p.Leu172Gln)
17g.41586321G>ACA499991583KRT14c.514C>T (p.Leu172=)
gnomAD v4
17g.41586321G>CCA399481713KRT14c.514C>G (p.Leu172Val)
17g.41586321G>TCA399481716KRT14c.514C>A (p.Leu172Met)
17g.41586322G>ACA499991592KRT14c.513C>T (p.Asp171=)
dbSNP
17g.41586322G>CCA399481718KRT14c.513C>G (p.Asp171Glu)
17g.41586322G=CA2260086766KRT14c.513C= (p.Asp171=)
17g.41586322G>TCA399481720KRT14c.513C>A (p.Asp171Glu)
17g.41586323T>ACA399481724KRT14c.512A>T (p.Asp171Val)
17g.41586323T>CCA399481725KRT14c.512A>G (p.Asp171Gly)
17g.41586323T>GCA399481728KRT14c.512A>C (p.Asp171Ala)
17g.41586324C>ACA399481732KRT14c.511G>T (p.Asp171Tyr)
17g.41586324C>GCA399481734KRT14c.511G>C (p.Asp171His)
17g.41586324C>TCA399481737KRT14c.511G>A (p.Asp171Asn)
17g.41586325C>ACA399481739KRT14c.510G>T (p.Glu170Asp)
17g.41586325C>GCA399481740KRT14c.510G>C (p.Glu170Asp)
17g.41586325C>TCA499991607KRT14c.510G>A (p.Glu170=)
17g.41586326T>ACA399481747KRT14c.509A>T (p.Glu170Val)
17g.41586326T>CCA399481742KRT14c.509A>G (p.Glu170Gly)
17g.41586326T>GCA399481744KRT14c.509A>C (p.Glu170Ala)
17g.41586327C>ACA399481750KRT14c.508G>T (p.Glu170Ter)
17g.41586327C=CA2260086767KRT14c.508G= (p.Glu170=)
17g.41586327C>GCA399481752KRT14c.508G>C (p.Glu170Gln)
17g.41586327C>TCA8562705KRT14c.508G>A (p.Glu170Lys)
dbSNP ExAC gnomAD v2 gnomAD v4
17g.41586328A=CA2260086768KRT14c.507T= (p.Ile169=)
17g.41586328A>CCA399481756KRT14c.507T>G (p.Ile169Met)
17g.41586328A>GCA8562706KRT14c.507T>C (p.Ile169=)
dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC
17g.41586328A>TCA499991627KRT14c.507T>A (p.Ile169=)
17g.41586329A=CA2260086769KRT14c.506T= (p.Ile169=)
17g.41586329A>CCA399481764KRT14c.506T>G (p.Ile169Ser)
17g.41586329A>GCA8562707KRT14c.506T>C (p.Ile169Thr)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.41586329A>TCA399481768KRT14c.506T>A (p.Ile169Asn)
17g.41586330T>ACA399481770KRT14c.505A>T (p.Ile169Phe)
17g.41586330T>CCA399481771KRT14c.505A>G (p.Ile169Val)
gnomAD v4
17g.41586330T>GCA399481777KRT14c.505A>C (p.Ile169Leu)
17g.41586331G>ACA499991642KRT14c.504C>T (p.Thr168=)
17g.41586331G>CCA499991647KRT14c.504C>G (p.Thr168=)
17g.41586331G>TCA499991645KRT14c.504C>A (p.Thr168=)
17g.41586332G>ACA399481785KRT14c.503C>T (p.Thr168Ile)
17g.41586332G>CCA399481784KRT14c.503C>G (p.Thr168Ser)
17g.41586332G>TCA399481781KRT14c.503C>A (p.Thr168Asn)
gnomAD v4
17g.41586333T>ACA399481788KRT14c.502A>T (p.Thr168Ser)
17g.41586333T>CCA399481791KRT14c.502A>G (p.Thr168Ala)
17g.41586333T>GCA399481793KRT14c.502A>C (p.Thr168Pro)
17g.41586334C>ACA8562708KRT14c.501G>T (p.Lys167Asn)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.41586334C=CA2260086770KRT14c.501G= (p.Lys167=)
17g.41586334C>GCA399481796KRT14c.501G>C (p.Lys167Asn)
17g.41586334C>TCA499991659KRT14c.501G>A (p.Lys167=)
dbSNP
17g.41586335T>ACA399481800KRT14c.500A>T (p.Lys167Met)
17g.41586335T>CCA399481802KRT14c.500A>G (p.Lys167Arg)
COSMIC
17g.41586335T>GCA399481803KRT14c.500A>C (p.Lys167Thr)
17g.41586336T>ACA399481808KRT14c.499A>T (p.Lys167Ter)
17g.41586336T>CCA399481810KRT14c.499A>G (p.Lys167Glu)
17g.41586336T>GCA399481812KRT14c.499A>C (p.Lys167Gln)
17g.41586337G>ACA499991670KRT14c.498C>T (p.Phe166=)
17g.41586337G>CCA399481816KRT14c.498C>G (p.Phe166Leu)
17g.41586337G>TCA399481819KRT14c.498C>A (p.Phe166Leu)
17g.41586338A>CCA399481826KRT14c.497T>G (p.Phe166Cys)
17g.41586338A>GCA399481824KRT14c.497T>C (p.Phe166Ser)
gnomAD v4
17g.41586338A>TCA399481822KRT14c.497T>A (p.Phe166Tyr)
17g.41586339A>CCA399481828KRT14c.496T>G (p.Phe166Val)
17g.41586339A>GCA399481830KRT14c.496T>C (p.Phe166Leu)
17g.41586339A>TCA399481833KRT14c.496T>A (p.Phe166Ile)
17g.41586340G>ACA499991702KRT14c.495C>T (p.Tyr165=)
17g.41586340G>CCA399481835KRT14c.495C>G (p.Tyr165Ter)
17g.41586340G>TCA399481836KRT14c.495C>A (p.Tyr165Ter)
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

Number of alleles fetched