Chr Mutation (hg38) CAid Gene Transcript Linkouts
17g.41586366_41586367delCA8562712KRT14c.468_469del (p.Ala157Ter)
dbSNP ExAC gnomAD
17g.41586367A>CCA499991836KRT14c.468T>G (p.Pro156=)
17g.41586367A>GCA499991837KRT14c.468T>C (p.Pro156=)
17g.41586367A>TCA499991838KRT14c.468T>A (p.Pro156=)
17g.41586368G>ACA399481987KRT14c.467C>T (p.Pro156Leu)
17g.41586368G>CCA399481988KRT14c.467C>G (p.Pro156Arg)
17g.41586368G>TCA399481991KRT14c.467C>A (p.Pro156His)
17g.41586369G>ACA399482002KRT14c.466C>T (p.Pro156Ser)
17g.41586369G>CCA399482000KRT14c.466C>G (p.Pro156Ala)
17g.41586369G>TCA399481994KRT14c.466C>A (p.Pro156Thr)
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>GCA399482005KRT14c.464G>C (p.Arg155Pro)
17g.41586371C>TCA8562714KRT14c.464G>A (p.Arg155Gln)
dbSNP ExAC gnomAD COSMIC
17g.41586372G>ACA8562715KRT14c.463C>T (p.Arg155Trp)
dbSNP ExAC gnomAD
17g.41586372G>CCA399482016KRT14c.463C>G (p.Arg155Gly)
17g.41586372G>TCA499991846KRT14c.463C>A (p.Arg155=)
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)
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>GCA8562716KRT14c.456G>C (p.Gln152His)
dbSNP ExAC gnomAD
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)
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)

Number of alleles fetched