Chr Mutation (hg38) CAid Gene Transcript Linkouts
19g.15540516C>ACA505828169CYP4F22c.738C>A (p.Arg246=)
19g.15540516C>GCA505828170CYP4F22c.738C>G (p.Arg246=)
19g.15540516C>TCA505828171CYP4F22c.738C>T (p.Arg246=)
19g.15540517T>ACA404535600CYP4F22c.739T>A (p.Leu247Met)
19g.15540517T>CCA505828172CYP4F22c.739T>C (p.Leu247=)
19g.15540517T>GCA404535602CYP4F22c.739T>G (p.Leu247Val)
19g.15540518T>ACA404535605CYP4F22c.740T>A (p.Leu247Ter)
19g.15540518T>CCA404535608CYP4F22c.740T>C (p.Leu247Ser)
19g.15540518T>GCA404535604CYP4F22c.740T>G (p.Leu247Trp)
19g.15540519G>ACA505828173CYP4F22c.741G>A (p.Leu247=)
19g.15540519G>CCA404535611CYP4F22c.741G>C (p.Leu247Phe)
19g.15540519G>TCA404535609CYP4F22c.741G>T (p.Leu247Phe)
19g.15540520C>ACA404535614CYP4F22c.742C>A (p.His248Asn)
19g.15540520C>GCA404535613CYP4F22c.742C>G (p.His248Asp)
19g.15540520C>TCA404535615CYP4F22c.742C>T (p.His248Tyr)
19g.15540521A=CA2324927924CYP4F22c.743A= (p.His248=)
19g.15540521A>CCA404535616CYP4F22c.743A>C (p.His248Pro)
19g.15540521A>GCA404535618CYP4F22c.743A>G (p.His248Arg)
dbSNP
19g.15540521A>TCA404535617CYP4F22c.743A>T (p.His248Leu)
19g.15540522C>ACA404535619CYP4F22c.744C>A (p.His248Gln)
19g.15540522C>GCA404535620CYP4F22c.744C>G (p.His248Gln)
19g.15540522C>TCA505828174CYP4F22c.744C>T (p.His248=)
gnomAD v4
19g.15540523C>ACA404535621CYP4F22c.745C>A (p.His249Asn)
19g.15540523C=CA2324927925CYP4F22c.745C= (p.His249=)
19g.15540523C>GCA404535622CYP4F22c.745C>G (p.His249Asp)
19g.15540523C>TCA404535623CYP4F22c.745C>T (p.His249Tyr)
dbSNP
19g.15540524A=CA2324927926CYP4F22c.746A= (p.His249=)
19g.15540524A>CCA404535624CYP4F22c.746A>C (p.His249Pro)
19g.15540524A>GCA404535625CYP4F22c.746A>G (p.His249Arg)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.15540524A>TCA404535626CYP4F22c.746A>T (p.His249Leu)
19g.15540525C>ACA404535627CYP4F22c.747C>A (p.His249Gln)
19g.15540525C>GCA404535628CYP4F22c.747C>G (p.His249Gln)
19g.15540525C>TCA505828175CYP4F22c.747C>T (p.His249=)
gnomAD v4
19g.15540526T>ACA404535629CYP4F22c.748T>A (p.Tyr250Asn)
19g.15540526T>CCA404535630CYP4F22c.748T>C (p.Tyr250His)
ClinVar dbSNP gnomAD v4
19g.15540526T>GCA404535631CYP4F22c.748T>G (p.Tyr250Asp)
19g.15540526T=CA2324927927CYP4F22c.748T= (p.Tyr250=)
19g.15540527A>CCA404535632CYP4F22c.749A>C (p.Tyr250Ser)
gnomAD v4
19g.15540527A>GCA404535634CYP4F22c.749A>G (p.Tyr250Cys)
19g.15540527A>TCA404535633CYP4F22c.749A>T (p.Tyr250Phe)
19g.15540528C>ACA404535635CYP4F22c.750C>A (p.Tyr250Ter)
19g.15540528C>GCA404535636CYP4F22c.750C>G (p.Tyr250Ter)
19g.15540528C>TCA505828176CYP4F22c.750C>T (p.Tyr250=)
19g.15540529C>ACA404535637CYP4F22c.751C>A (p.Leu251Ile)
19g.15540529C>GCA404535638CYP4F22c.751C>G (p.Leu251Val)
19g.15540529C>TCA404535639CYP4F22c.751C>T (p.Leu251Phe)
gnomAD v4
19g.15540530T>ACA404535640CYP4F22c.752T>A (p.Leu251His)
19g.15540530T>CCA404535641CYP4F22c.752T>C (p.Leu251Pro)
19g.15540530T>GCA404535642CYP4F22c.752T>G (p.Leu251Arg)
19g.15540531C>ACA505828177CYP4F22c.753C>A (p.Leu251=)

Number of alleles fetched