Colon Cancer: Gene >> CXCL5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000296027
Start	73998224:73998224(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756143598
CDS Mutation	c.224G>A
AA Mutation	p.Cys75Tyr(p.C75Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000296027
Start	73998326:73998326(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.122C>T
AA Mutation	p.Ala41Val(p.A41V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000296027
Start	73998024:73998024(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.314A>C
AA Mutation	p.Lys105Thr(p.K105T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000296027
Start	73998565:73998565(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.17G>T
AA Mutation	p.Ser6Ile(p.S6I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000296027
Start	73998524:73998524(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.58G>A
AA Mutation	p.Ala20Thr(p.A20T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000296027
Start	73998525:73998525(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749214767
CDS Mutation	c.57C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> CXCL5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000296027
Start	73998073:73998073(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.265G>A
AA Mutation	p.Glu89Lys(p.E89K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000296027
Start	73998289:73998289(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.159G>T
AA Mutation	p.Gln53His(p.Q53H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript