Colon Cancer: Gene >> CAMP

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000296435
Start	48225366:48225366(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760073514
CDS Mutation	c.464G>T
AA Mutation	p.Arg155Ile(p.R155I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000296435
Start	48224458:48224458(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201842351
CDS Mutation	c.315C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000296435
Start	48224419:48224419(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762582408
CDS Mutation	c.276G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> CAMP

Mutation ID	1
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000296435
Start	48224646:48224646(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.365delG
AA Mutation	p.Gly122AlafsTer65(p.G122Afs*65)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript