Chr Mutation (hg38) CAid Gene Transcript Linkouts
19g.1220449A>TCA402949100STK11c.541A>T (p.Asn181Tyr)
c.169A>T (p.Asn57Tyr)
c.367A>T (p.Asn123Tyr)
n.364A>T
n.631A>T
n.437A>T
c.319A>T (p.Asn107Tyr)
n.1166A>T
dbSNP COSMIC COSMIC
19g.1220449A>CCA402949093STK11c.541A>C (p.Asn181His)
c.169A>C (p.Asn57His)
c.367A>C (p.Asn123His)
n.364A>C
n.631A>C
n.437A>C
c.319A>C (p.Asn107His)
n.1166A>C
dbSNP
19g.1220449A>GCA10586375STK11c.541A>G (p.Asn181Asp)
c.169A>G (p.Asn57Asp)
c.367A>G (p.Asn123Asp)
n.364A>G
n.631A>G
n.437A>G
c.319A>G (p.Asn107Asp)
n.1166A>G
ClinVar dbSNP
19g.1220449A=CA2317589783STK11c.541A= (p.Asn181=)
c.169A= (p.Asn57=)
c.367A= (p.Asn123=)
n.364A=
n.631A=
n.437A=
c.319A= (p.Asn107=)
n.1166A=
dbSNP

Number of alleles fetched