Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> FDPS

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000356657
Start 155320581:155320581(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1232C>T
AA Mutation p.Ala411Val(p.A411V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000356657
Start 155310155:155310155(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.289G>C
AA Mutation p.Asp97His(p.D97H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000356657
Start 155309955:155309955(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.166G>A
AA Mutation p.Glu56Lys(p.E56K)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000356657
Start 155318678:155318678(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.698C>G
AA Mutation p.Thr233Ser(p.T233S)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000356657
Start 155320515:155320515(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1166G>A
AA Mutation p.Ser389Asn(p.S389N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000356657
Start 155317947:155317947(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.487G>A
AA Mutation p.Ala163Thr(p.A163T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000356657
Start 155312310:155312310(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.395T>A
AA Mutation p.Val132Glu(p.V132E)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 8
Mutation Consequence frameshift_variant
Transcription ID ENST00000356657
Start 155309853:155309853(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.67delC
AA Mutation p.Arg23GlyfsTer45(p.R23Gfs*45)
Mutation Classification Frame_Shift_Del
Feature Type Transcript

Rectum Cancer: Gene >> FDPS

No Mutation Annotation!