Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> BTG3

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000348354
Start 17598817:17598817(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.319G>C
AA Mutation p.Glu107Gln(p.E107Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000348354
Start 17594167:17594167(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.685A>G
AA Mutation p.Thr229Ala(p.T229A)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence synonymous_variant
Transcription ID ENST00000348354
Start 17604955:17604955(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.216C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 4
Mutation Consequence frameshift_variant;start_lost
Transcription ID ENST00000348354
Start 17609144:17609144(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.1delA
AA Mutation p.Met1?(p.M1?)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 5
Mutation Consequence stop_gained
Transcription ID ENST00000348354
Start 17609096:17609096(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.49C>T
AA Mutation p.Arg17Ter(p.R17*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript

Rectum Cancer: Gene >> BTG3

No Mutation Annotation!