Chr Mutation (hg38) CAid Gene Transcript Linkouts
17g.41586412_41586473delCA645584614KRT14c.362_423del (p.Asn121ArgfsTer8)
COSMIC
17g.41586467T>ACA399482536KRT14c.368A>T (p.Asn123Ile)
17g.41586467T>CCA216911KRT14c.368A>G (p.Asn123Ser)
ClinVar dbSNP
17g.41586467T>GCA399482537KRT14c.368A>C (p.Asn123Thr)
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
17g.41586471G>CCA399482550KRT14c.364C>G (p.Leu122Val)
17g.41586471G>TCA399482552KRT14c.364C>A (p.Leu122Ile)
17g.41586472G>ACA8562734KRT14c.363C>T (p.Asn121=)
dbSNP ExAC gnomAD
17g.41586472G>CCA399482554KRT14c.363C>G (p.Asn121Lys)
17g.41586472G>TCA399482556KRT14c.363C>A (p.Asn121Lys)
17g.41586473T>ACA399482558KRT14c.362A>T (p.Asn121Ile)
17g.41586473T>CCA399482560KRT14c.362A>G (p.Asn121Ser)
17g.41586473T>GCA399482562KRT14c.362A>C (p.Asn121Thr)
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.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>GCA399482582KRT14c.357G>C (p.Met119Ile)
17g.41586478C>TCA216903KRT14c.357G>A (p.Met119Ile)
ClinVar dbSNP
17g.41586479A>CCA399482585KRT14c.356T>G (p.Met119Arg)
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.41586481G>ACA499992007KRT14c.354C>T (p.Thr118=)
17g.41586481G>CCA499992008KRT14c.354C>G (p.Thr118=)
17g.41586481G>TCA8562735KRT14c.354C>A (p.Thr118=)
dbSNP ExAC
17g.41586482G>ACA16620405KRT14c.353C>T (p.Thr118Ile)
ClinVar gnomAD
17g.41586482G>CCA399482594KRT14c.353C>G (p.Thr118Ser)
17g.41586482G>TCA399482596KRT14c.353C>A (p.Thr118Asn)
17g.41586483T>ACA399482599KRT14c.352A>T (p.Thr118Ser)

Number of alleles fetched