Chr Mutation (hg38) CAid Gene Transcript Linkouts
19g.1220450A>CCA402949102STK11c.542A>C (p.Asn181Thr)
c.170A>C (p.Asn57Thr)
c.368A>C (p.Asn123Thr)
n.365A>C
n.632A>C
n.438A>C
c.320A>C (p.Asn107Thr)
n.1167A>C
dbSNP
19g.1220450A>TCA402949107STK11c.542A>T (p.Asn181Ile)
c.170A>T (p.Asn57Ile)
c.368A>T (p.Asn123Ile)
n.365A>T
n.632A>T
n.438A>T
c.320A>T (p.Asn107Ile)
n.1167A>T
dbSNP COSMIC COSMIC
19g.1220450A>GCA10586687STK11c.542A>G (p.Asn181Ser)
c.170A>G (p.Asn57Ser)
c.368A>G (p.Asn123Ser)
n.365A>G
n.632A>G
n.438A>G
c.320A>G (p.Asn107Ser)
n.1167A>G
ClinVar dbSNP

Number of alleles fetched