Chr Mutation (hg38) CAid Gene Transcript Linkouts
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)

Number of alleles fetched