Chr Mutation (hg38) CAid Gene Transcript Linkouts
19g.1205800_1207204dupCA1139666174STK11c.-1114_290+1dup
c.-82-12617_-82-11213dup (p.=)
ClinVar
19g.1205800_1207204delCA891843672STK11c.-1114_290+1del
c.-82-12617_-82-11213del (p.=)
ClinVar
19g.1206912_1208216delCA2499225350STK11c.-2_290+1013del
c.-82-11505_-82-10201del (p.=)
n.89_380+1013del
c.-355_-64+1013del
n.624_915+1013del
ClinVar
19g.1206913C=CA2317581529STK11c.-1C= (p.=)
c.-82-11504C= (p.=)
n.90C=
c.-354C= (p.=)
n.625C=
19g.1206913C>TCA022704STK11c.-1C>T (p.=)
c.-82-11504C>T (p.=)
n.90C>T
c.-354C>T (p.=)
n.625C>T
ClinVar dbSNP ExAC gnomAD
19g.1206914A=CA2317581530STK11c.1A=
c.-82-11503A= (p.=)
n.91A=
c.-353A= (p.=)
n.626A=
19g.1206914A>CCA402942866STK11c.1A>C
c.-82-11503A>C (p.=)
n.91A>C
c.-353A>C (p.=)
n.626A>C
19g.1206914A>GCA402942869STK11c.1A>G
c.-82-11503A>G (p.=)
n.91A>G
c.-353A>G (p.=)
n.626A>G
19g.1206914A>TCA402942875STK11c.1A>T
c.-82-11503A>T (p.=)
n.91A>T
c.-353A>T (p.=)
n.626A>T
ClinVar
19g.1206915T>ACA402942885STK11c.2T>A
c.-82-11502T>A (p.=)
n.92T>A
c.-352T>A (p.=)
n.627T>A
19g.1206915T>CCA402942887STK11c.2T>C
c.-82-11502T>C (p.=)
n.92T>C
c.-352T>C (p.=)
n.627T>C
COSMIC
19g.1206915T>GCA402942891STK11c.2T>G
c.-82-11502T>G (p.=)
n.92T>G
c.-352T>G (p.=)
n.627T>G
19g.1206916G>ACA402942899STK11c.3G>A
c.-82-11501G>A (p.=)
n.93G>A
c.-351G>A (p.=)
n.628G>A
19g.1206916G>CCA402942905STK11c.3G>C
c.-82-11501G>C (p.=)
n.93G>C
c.-351G>C (p.=)
n.628G>C
19g.1206916G>TCA402942901STK11c.3G>T
c.-82-11501G>T (p.=)
n.93G>T
c.-351G>T (p.=)
n.628G>T
19g.1206917G>ACA402942910STK11c.4G>A (p.Glu2Lys)
c.-82-11500G>A (p.=)
n.94G>A
c.-350G>A (p.=)
n.629G>A
19g.1206917G>CCA402942914STK11c.4G>C (p.Glu2Gln)
c.-82-11500G>C (p.=)
n.94G>C
c.-350G>C (p.=)
n.629G>C
ClinVar
19g.1206917G=CA2317581531STK11c.4G= (p.Glu2=)
c.-82-11500G= (p.=)
n.94G=
c.-350G= (p.=)
n.629G=
19g.1206917G>TCA402942915STK11c.4G>T (p.Glu2Ter)
c.-82-11500G>T (p.=)
n.94G>T
c.-350G>T (p.=)
n.629G>T
19g.1206918A=CA2317581532STK11c.5A= (p.Glu2=)
c.-82-11499A= (p.=)
n.95A=
c.-349A= (p.=)
n.630A=
19g.1206918A>CCA402942916STK11c.5A>C (p.Glu2Ala)
c.-82-11499A>C (p.=)
n.95A>C
c.-349A>C (p.=)
n.630A>C
ClinVar gnomAD
19g.1206918A>GCA402942917STK11c.5A>G (p.Glu2Gly)
c.-82-11499A>G (p.=)
n.95A>G
c.-349A>G (p.=)
n.630A>G
19g.1206918A>TCA402942918STK11c.5A>T (p.Glu2Val)
c.-82-11499A>T (p.=)
n.95A>T
c.-349A>T (p.=)
n.630A>T
19g.1206918_1206921delinsAGGTCA2317581533STK11c.5_8delinsAGGT (p.Glu2=)
c.-82-11499_-82-11496delinsAGGT (p.=)
n.95_98delinsAGGT
c.-349_-346delinsAGGT (p.=)
n.630_633delinsAGGT
19g.1206919G>ACA504706061STK11c.6G>A (p.Glu2=)
c.-82-11498G>A (p.=)
n.96G>A
c.-348G>A (p.=)
n.631G>A
ClinVar gnomAD
19g.1206919G>CCA402942919STK11c.6G>C (p.Glu2Asp)
c.-82-11498G>C (p.=)
n.96G>C
c.-348G>C (p.=)
n.631G>C
19g.1206919G=CA2317581534STK11c.6G= (p.Glu2=)
c.-82-11498G= (p.=)
n.96G=
c.-348G= (p.=)
n.631G=
19g.1206919G>TCA402942920STK11c.6G>T (p.Glu2Asp)
c.-82-11498G>T (p.=)
n.96G>T
c.-348G>T (p.=)
n.631G>T
19g.1206924_1206926delCA658656737STK11c.11_13del (p.Val4del)
c.-82-11493_-82-11491del (p.=)
n.101_103del
c.-343_-341del (p.=)
n.636_638del
dbSNP
19g.1206920G>ACA16620743STK11c.7G>A (p.Val3Met)
c.-82-11497G>A (p.=)
n.97G>A
c.-347G>A (p.=)
n.632G>A
ClinVar
19g.1206920G>CCA304016681STK11c.7G>C (p.Val3Leu)
c.-82-11497G>C (p.=)
n.97G>C
c.-347G>C (p.=)
n.632G>C
ClinVar dbSNP
19g.1206920G=CA2317581535STK11c.7G= (p.Val3=)
c.-82-11497G= (p.=)
n.97G=
c.-347G= (p.=)
n.632G=
19g.1206920G>TCA402942937STK11c.7G>T (p.Val3Leu)
c.-82-11497G>T (p.=)
n.97G>T
c.-347G>T (p.=)
n.632G>T
19g.1206921T>ACA402942943STK11c.8T>A (p.Val3Glu)
c.-82-11496T>A (p.=)
n.98T>A
c.-346T>A (p.=)
n.633T>A
19g.1206921T>CCA402942952STK11c.8T>C (p.Val3Ala)
c.-82-11496T>C (p.=)
n.98T>C
c.-346T>C (p.=)
n.633T>C
19g.1206921T>GCA10652247STK11c.8T>G (p.Val3Gly)
c.-82-11496T>G (p.=)
n.98T>G
c.-346T>G (p.=)
n.633T>G
ClinVar dbSNP
19g.1206921T=CA2317581536STK11c.8T= (p.Val3=)
c.-82-11496T= (p.=)
n.98T=
c.-346T= (p.=)
n.633T=
19g.1206922G>ACA504706062STK11c.9G>A (p.Val3=)
c.-82-11495G>A (p.=)
n.99G>A
c.-345G>A (p.=)
n.634G>A
ClinVar
19g.1206922G>CCA504706064STK11c.9G>C (p.Val3=)
c.-82-11495G>C (p.=)
n.99G>C
c.-345G>C (p.=)
n.634G>C
19g.1206922G=CA2317581537STK11c.9G= (p.Val3=)
c.-82-11495G= (p.=)
n.99G=
c.-345G= (p.=)
n.634G=
19g.1206922G>TCA504706063STK11c.9G>T (p.Val3=)
c.-82-11495G>T (p.=)
n.99G>T
c.-345G>T (p.=)
n.634G>T
19g.1206923G>ACA402942954STK11c.10G>A (p.Val4Met)
c.-82-11494G>A (p.=)
n.100G>A
c.-344G>A (p.=)
n.635G>A
ClinVar COSMIC
19g.1206923G>CCA045160STK11c.10G>C (p.Val4Leu)
c.-82-11494G>C (p.=)
n.100G>C
c.-344G>C (p.=)
n.635G>C
ClinVar dbSNP ExAC
19g.1206923G=CA2317581538STK11c.10G= (p.Val4=)
c.-82-11494G= (p.=)
n.100G=
c.-344G= (p.=)
n.635G=
19g.1206923G>TCA402942957STK11c.10G>T (p.Val4Leu)
c.-82-11494G>T (p.=)
n.100G>T
c.-344G>T (p.=)
n.635G>T
ClinVar
19g.1206924T>ACA402942972STK11c.11T>A (p.Val4Glu)
c.-82-11493T>A (p.=)
n.101T>A
c.-343T>A (p.=)
n.636T>A
19g.1206924T>CCA402942988STK11c.11T>C (p.Val4Ala)
c.-82-11493T>C (p.=)
n.101T>C
c.-343T>C (p.=)
n.636T>C
ClinVar
19g.1206924T>GCA402942973STK11c.11T>G (p.Val4Gly)
c.-82-11493T>G (p.=)
n.101T>G
c.-343T>G (p.=)
n.636T>G
19g.1206924T=CA2317581539STK11c.11T= (p.Val4=)
c.-82-11493T= (p.=)
n.101T=
c.-343T= (p.=)
n.636T=
19g.1206925G>ACA504706065STK11c.12G>A (p.Val4=)
c.-82-11492G>A (p.=)
n.102G>A
c.-342G>A (p.=)
n.637G>A
ClinVar gnomAD

Number of alleles fetched