Colon Cancer: Gene >> CXCL8

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000307407
Start	73741620:73741620(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.143T>G
AA Mutation	p.Phe48Cys(p.F48C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000307407
Start	73742008:73742008(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.260G>T
AA Mutation	p.Arg87Met(p.R87M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	frameshift_variant;stop_lost
Transcription ID	ENST00000307407
Start	73742463:73742463(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.*5delA
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> CXCL8

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000307407
Start	73742455:73742455(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.291G>T
AA Mutation	p.Glu97Asp(p.E97D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript