Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> BOLL

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000392296
Start 197779060:197779060(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs778462794
CDS Mutation c.136G>A
AA Mutation p.Glu46Lys(p.E46K)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000392296
Start 197781831:197781831(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.20C>T
AA Mutation p.Ser7Phe(p.S7F)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000392296
Start 197777103:197777103(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs577424738
CDS Mutation c.232G>A
AA Mutation p.Val78Ile(p.V78I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000392296
Start 197771874:197771874(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs750315080
CDS Mutation c.461C>T
AA Mutation p.Ser154Leu(p.S154L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence inframe_insertion
Transcription ID ENST00000392296
Start 197771933:197771934(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.401_402insATTGATAGTAATAGA
AA Mutation p.Thr134_Gly135insLeuIleValIleAsp(p.T134_G135insLIVID)
Mutation Classification In_Frame_Ins
Feature Type Transcript
Mutation ID 6
Mutation Consequence stop_lost
Transcription ID ENST00000392296
Start 197728555:197728555(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.852A>T
AA Mutation p.Ter284TyrextTer11(p.*284Yext*11)
Mutation Classification Nonstop_Mutation
Feature Type Transcript

Rectum Cancer: Gene >> BOLL

No Mutation Annotation!