Chr Mutation (hg38) CAid Gene Transcript Linkouts
12g.25209791_25209795delCA2022884500KRASc.*124_*128del (p.=)
c.*3_*7del
dbSNP
12g.25209795T>ACA384148272KRASc.*121A>T (p.=)
c.567A>T (p.Ter189Tyr)
c.228A>T (p.Ter76Tyr)
12g.25209795T>GCA384148273KRASc.*121A>C (p.=)
c.567A>C (p.Ter189Tyr)
c.228A>C (p.Ter76Tyr)
12g.25209796T>ACA384148274KRASc.*120A>T (p.=)
c.566A>T (p.Ter189Leu)
c.227A>T (p.Ter76Leu)
12g.25209796T>GCA384148275KRASc.*120A>C (p.=)
c.566A>C (p.Ter189Ser)
c.227A>C (p.Ter76Ser)
12g.25209797A>CCA384148276KRASc.*119T>G (p.=)
c.565T>G (p.Ter189Glu)
c.226T>G (p.Ter76Glu)
12g.25209797A>GCA384148277KRASc.*119T>C (p.=)
c.565T>C (p.Ter189Gln)
c.226T>C (p.Ter76Gln)
12g.25209797A>TCA384148278KRASc.*119T>A (p.=)
c.565T>A (p.Ter189Lys)
c.226T>A (p.Ter76Lys)
12g.25209798C>ACA384148281KRASc.*118G>T (p.=)
c.564G>T (p.Met188Ile)
c.225G>T (p.Met75Ile)
12g.25209798C=CA2022884502KRASc.*118G= (p.=)
c.564G= (p.Met188=)
c.225G= (p.Met75=)
12g.25209798C>GCA384148280KRASc.*118G>C (p.=)
c.564G>C (p.Met188Ile)
c.225G>C (p.Met75Ile)
gnomAD
12g.25209798C>TCA384148279KRASc.*118G>A (p.=)
c.564G>A (p.Met188Ile)
c.225G>A (p.Met75Ile)
12g.25209799A>CCA384148282KRASc.*117T>G (p.=)
c.563T>G (p.Met188Arg)
c.224T>G (p.Met75Arg)
12g.25209799A>GCA384148283KRASc.*117T>C (p.=)
c.563T>C (p.Met188Thr)
c.224T>C (p.Met75Thr)
12g.25209799A>TCA384148284KRASc.*117T>A (p.=)
c.563T>A (p.Met188Lys)
c.224T>A (p.Met75Lys)
12g.25209800T>ACA384148285KRASc.*116A>T (p.=)
c.562A>T (p.Met188Leu)
c.223A>T (p.Met75Leu)
12g.25209800T>CCA384148286KRASc.*116A>G (p.=)
c.562A>G (p.Met188Val)
c.223A>G (p.Met75Val)
12g.25209800T>GCA384148287KRASc.*116A>C (p.=)
c.562A>C (p.Met188Leu)
c.223A>C (p.Met75Leu)
COSMIC
12g.25209800T=CA2022884506KRASc.*116A= (p.=)
c.562A= (p.Met188=)
c.223A= (p.Met75=)
12g.25209801A>CCA384148288KRASc.*115T>G (p.=)
c.561T>G (p.Ile187Met)
c.222T>G (p.Ile74Met)
12g.25209802A>CCA384148289KRASc.*114T>G (p.=)
c.560T>G (p.Ile187Ser)
c.221T>G (p.Ile74Ser)
12g.25209802A>GCA384148290KRASc.*114T>C (p.=)
c.560T>C (p.Ile187Thr)
c.221T>C (p.Ile74Thr)
12g.25209802A>TCA384148291KRASc.*114T>A (p.=)
c.560T>A (p.Ile187Asn)
c.221T>A (p.Ile74Asn)
12g.25209803T>ACA384148292KRASc.*113A>T (p.=)
c.559A>T (p.Ile187Phe)
c.220A>T (p.Ile74Phe)
12g.25209803T>CCA384148293KRASc.*113A>G (p.=)
c.559A>G (p.Ile187Val)
c.220A>G (p.Ile74Val)
12g.25209803T>GCA384148294KRASc.*113A>C (p.=)
c.559A>C (p.Ile187Leu)
c.220A>C (p.Ile74Leu)
12g.25209803T=CA2022884509KRASc.*113A= (p.=)
c.559A= (p.Ile187=)
c.220A= (p.Ile74=)
12g.25209804_25209806delinsTACCA2022884511KRASc.*110_*112delinsGTA (p.=)
c.556_558delinsGTA (p.Val186=)
c.217_219delinsGTA (p.Val73=)
12g.25209805A>CCA384148297KRASc.*111T>G (p.=)
c.557T>G (p.Val186Gly)
c.218T>G (p.Val73Gly)
12g.25209805A>GCA384148296KRASc.*111T>C (p.=)
c.557T>C (p.Val186Ala)
c.218T>C (p.Val73Ala)
12g.25209805A>TCA384148295KRASc.*111T>A (p.=)
c.557T>A (p.Val186Glu)
c.218T>A (p.Val73Glu)
12g.25209809_25209810delCA603691324KRASc.*110_*111del (p.=)
c.556_557del (p.Val186AsnfsTer25)
c.217_218del (p.Val73AsnfsTer25)
dbSNP gnomAD
12g.25209806C>ACA384148300KRASc.*110G>T (p.=)
c.556G>T (p.Val186Leu)
c.217G>T (p.Val73Leu)
ClinVar
12g.25209806C=CA2022884515KRASc.*110G= (p.=)
c.556G= (p.Val186=)
c.217G= (p.Val73=)
12g.25209806C>GCA384148298KRASc.*110G>C (p.=)
c.556G>C (p.Val186Leu)
c.217G>C (p.Val73Leu)
12g.25209806C>TCA384148299KRASc.*110G>A (p.=)
c.556G>A (p.Val186Ile)
c.217G>A (p.Val73Ile)
gnomAD
12g.25209807A>CCA384148301KRASc.*109T>G (p.=)
c.555T>G (p.Cys185Trp)
c.216T>G (p.Cys72Trp)
12g.25209807A>TCA384148302KRASc.*109T>A (p.=)
c.555T>A (p.Cys185Ter)
c.216T>A (p.Cys72Ter)
12g.25209808C>ACA384148303KRASc.*108G>T (p.=)
c.554G>T (p.Cys185Phe)
c.215G>T (p.Cys72Phe)
12g.25209808C=CA2022884520KRASc.*108G= (p.=)
c.554G= (p.Cys185=)
c.215G= (p.Cys72=)
12g.25209808C>GCA384148304KRASc.*108G>C (p.=)
c.554G>C (p.Cys185Ser)
c.215G>C (p.Cys72Ser)
12g.25209808C>TCA6486820KRASc.*108G>A (p.=)
c.554G>A (p.Cys185Tyr)
c.215G>A (p.Cys72Tyr)
dbSNP ExAC gnomAD
12g.25209809A>CCA384148305KRASc.*107T>G (p.=)
c.553T>G (p.Cys185Gly)
c.214T>G (p.Cys72Gly)
12g.25209809A>GCA384148306KRASc.*107T>C (p.=)
c.553T>C (p.Cys185Arg)
c.214T>C (p.Cys72Arg)
COSMIC
12g.25209809A>TCA384148307KRASc.*107T>A (p.=)
c.553T>A (p.Cys185Ser)
c.214T>A (p.Cys72Ser)
COSMIC
12g.25209809_25209815delinsACTTTGTCA2022884523KRASc.*101_*107delinsACAAAGT (p.=)
c.547_553delinsACAAAGT (p.Thr183=)
c.208_214delinsACAAAGT (p.Thr70=)
12g.25209810C>ACA384148308KRASc.*106G>T (p.=)
c.552G>T (p.Lys184Asn)
c.213G>T (p.Lys71Asn)
12g.25209810C>GCA384148309KRASc.*106G>C (p.=)
c.552G>C (p.Lys184Asn)
c.213G>C (p.Lys71Asn)
12g.25209815_25209820delCA603691326KRASc.*101_*106del (p.=)
c.547_552del (p.Thr183_Lys184del)
c.208_213del (p.Thr70_Lys71del)
ClinVar dbSNP gnomAD
12g.25209811T>ACA384148311KRASc.*105A>T (p.=)
c.551A>T (p.Lys184Met)
c.212A>T (p.Lys71Met)

Number of alleles fetched