Chr Mutation (hg38) CAid Gene Transcript Linkouts
12g.25215546dupCA234211604KRASc.469dup (p.Tyr157LeufsTer28)
c.451-5631dup (p.=)
c.112-5631dup (p.=)
dbSNP
12g.25215545A>CCA384149232KRASc.466T>G (p.Phe156Val)
c.451-5634T>G (p.=)
c.112-5634T>G (p.=)
12g.25215545A>GCA384149234KRASc.466T>C (p.Phe156Leu)
c.451-5634T>C (p.=)
c.112-5634T>C (p.=)
12g.25215545A>TCA384149237KRASc.466T>A (p.Phe156Ile)
c.451-5634T>A (p.=)
c.112-5634T>A (p.=)
12g.25215546A>CCA478889740KRASc.465T>G (p.Ala155=)
c.451-5635T>G (p.=)
c.112-5635T>G (p.=)
12g.25215546A>GCA478889741KRASc.465T>C (p.Ala155=)
c.451-5635T>C (p.=)
c.112-5635T>C (p.=)
12g.25215546A>TCA478889742KRASc.465T>A (p.Ala155=)
c.451-5635T>A (p.=)
c.112-5635T>A (p.=)
12g.25215547G>ACA384149245KRASc.464C>T (p.Ala155Val)
c.451-5636C>T (p.=)
c.112-5636C>T (p.=)
12g.25215547G>CCA384149240KRASc.464C>G (p.Ala155Gly)
c.451-5636C>G (p.=)
c.112-5636C>G (p.=)
12g.25215547G>TCA384149243KRASc.464C>A (p.Ala155Asp)
c.451-5636C>A (p.=)
c.112-5636C>A (p.=)
COSMIC
12g.25215548C>ACA384149248KRASc.463G>T (p.Ala155Ser)
c.451-5637G>T (p.=)
c.112-5637G>T (p.=)
12g.25215548C=CA2022890387KRASc.463G= (p.Ala155=)
c.451-5637G= (p.=)
c.112-5637G= (p.=)
12g.25215548C>GCA384149250KRASc.463G>C (p.Ala155Pro)
c.451-5637G>C (p.=)
c.112-5637G>C (p.=)
12g.25215548C>TCA384149252KRASc.463G>A (p.Ala155Thr)
c.451-5637G>A (p.=)
c.112-5637G>A (p.=)
12g.25215549A>CCA384149255KRASc.462T>G (p.Asp154Glu)
c.451-5638T>G (p.=)
c.112-5638T>G (p.=)
12g.25215549A>GCA478889746KRASc.462T>C (p.Asp154=)
c.451-5638T>C (p.=)
c.112-5638T>C (p.=)
12g.25215549A>TCA384149257KRASc.462T>A (p.Asp154Glu)
c.451-5638T>A (p.=)
c.112-5638T>A (p.=)
12g.25215550T>ACA384149261KRASc.461A>T (p.Asp154Val)
c.451-5639A>T (p.=)
c.112-5639A>T (p.=)
12g.25215550T>CCA234211615KRASc.461A>G (p.Asp154Gly)
c.451-5639A>G (p.=)
c.112-5639A>G (p.=)
dbSNP gnomAD
12g.25215550T>GCA384149265KRASc.461A>C (p.Asp154Ala)
c.451-5639A>C (p.=)
c.112-5639A>C (p.=)
12g.25215550T=CA2022890389KRASc.461A= (p.Asp154=)
c.451-5639A= (p.=)
c.112-5639A= (p.=)
12g.25215551C>ACA384149268KRASc.460G>T (p.Asp154Tyr)
c.451-5640G>T (p.=)
c.112-5640G>T (p.=)
12g.25215551C=CA2022890390KRASc.460G= (p.Asp154=)
c.451-5640G= (p.=)
c.112-5640G= (p.=)
12g.25215551C>GCA384149270KRASc.460G>C (p.Asp154His)
c.451-5640G>C (p.=)
c.112-5640G>C (p.=)
12g.25215551C>TCA384149272KRASc.460G>A (p.Asp154Asn)
c.451-5640G>A (p.=)
c.112-5640G>A (p.=)
12g.25215551_25215552insTCA686718321KRASc.459_460insA (p.Asp154ArgfsTer?)
c.451-5641_451-5640insA (p.=)
c.112-5641_112-5640insA (p.=)
dbSNP
12g.25215552C>ACA384149275KRASc.459G>T (p.Glu153Asp)
c.451-5641G>T (p.=)
c.112-5641G>T (p.=)
12g.25215552C>GCA384149277KRASc.459G>C (p.Glu153Asp)
c.451-5641G>C (p.=)
c.112-5641G>C (p.=)
12g.25215552C>TCA478889750KRASc.459G>A (p.Glu153=)
c.451-5641G>A (p.=)
c.112-5641G>A (p.=)
12g.25215553T>ACA384149280KRASc.458A>T (p.Glu153Val)
c.451-5642A>T (p.=)
c.112-5642A>T (p.=)
ClinVar
12g.25215553T>CCA384149285KRASc.458A>G (p.Glu153Gly)
c.451-5642A>G (p.=)
c.112-5642A>G (p.=)
12g.25215553T>GCA384149283KRASc.458A>C (p.Glu153Ala)
c.451-5642A>C (p.=)
c.112-5642A>C (p.=)
ClinVar
12g.25215553T=CA2022890391KRASc.458A= (p.Glu153=)
c.451-5642A= (p.=)
c.112-5642A= (p.=)
12g.25215554C>ACA384149289KRASc.457G>T (p.Glu153Ter)
c.451-5643G>T (p.=)
c.112-5643G>T (p.=)
12g.25215554C>GCA384149291KRASc.457G>C (p.Glu153Gln)
c.451-5643G>C (p.=)
c.112-5643G>C (p.=)
12g.25215554C>TCA384149293KRASc.457G>A (p.Glu153Lys)
c.451-5643G>A (p.=)
c.112-5643G>A (p.=)
12g.25215555C>ACA478889752KRASc.456G>T (p.Val152=)
c.451-5644G>T (p.=)
c.112-5644G>T (p.=)
12g.25215555C=CA2022890392KRASc.456G= (p.Val152=)
c.451-5644G= (p.=)
c.112-5644G= (p.=)
12g.25215555C>GCA478889753KRASc.456G>C (p.Val152=)
c.451-5644G>C (p.=)
c.112-5644G>C (p.=)
12g.25215555C>TCA478889754KRASc.456G>A (p.Val152=)
c.451-5644G>A (p.=)
c.112-5644G>A (p.=)
12g.25215556A>CCA384149296KRASc.455T>G (p.Val152Gly)
c.451-5645T>G (p.=)
c.112-5645T>G (p.=)
12g.25215556A>GCA384149298KRASc.455T>C (p.Val152Ala)
c.451-5645T>C (p.=)
c.112-5645T>C (p.=)
12g.25215556A>TCA384149300KRASc.455T>A (p.Val152Glu)
c.451-5645T>A (p.=)
c.112-5645T>A (p.=)
12g.25215556_25215558delinsACTCA2022890393KRASc.453_455delinsAGT (p.Arg151=)
c.451-5647_451-5645delinsAGT (p.=)
c.112-5647_112-5645delinsAGT (p.=)
12g.25215557C>ACA384149303KRASc.454G>T (p.Val152Leu)
c.451-5646G>T (p.=)
c.112-5646G>T (p.=)
12g.25215557C>GCA384149306KRASc.454G>C (p.Val152Leu)
c.451-5646G>C (p.=)
c.112-5646G>C (p.=)
12g.25215557C>TCA384149308KRASc.454G>A (p.Val152Met)
c.451-5646G>A (p.=)
c.112-5646G>A (p.=)
12g.25215561_25215562delCA919045445KRASc.453_454del
c.451-5647_451-5646del (p.=)
c.112-5647_112-5646del (p.=)
dbSNP
12g.25215558T>ACA384149311KRASc.453A>T (p.Arg151Ser)
c.451-5647A>T (p.=)
c.112-5647A>T (p.=)
12g.25215558T>CCA478889757KRASc.453A>G (p.Arg151=)
c.451-5647A>G (p.=)
c.112-5647A>G (p.=)

Number of alleles fetched