Colon Cancer: Gene >> CCK

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000334681
Start	42258138:42258138(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.308T>C
AA Mutation	p.Phe103Ser(p.F103S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000334681
Start	42263474:42263474(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.157G>A
AA Mutation	p.Glu53Lys(p.E53K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000334681
Start	42258132:42258132(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs11559016
CDS Mutation	c.314G>A
AA Mutation	p.Arg105His(p.R105H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000334681
Start	42263607:42263607(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.24C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000334681
Start	42263529:42263529(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.102G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000334681
Start	42258209:42258209(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.237C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> CCK

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000334681
Start	42263532:42263532(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.99G>A
Mutation Classification	Silent
Feature Type	Transcript