Colon Cancer: Gene >> OLA1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000284719
Start	174123184:174123184(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.724A>G
AA Mutation	p.Lys242Glu(p.K242E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000284719
Start	174229342:174229342(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748811959
CDS Mutation	c.211T>G
AA Mutation	p.Phe71Val(p.F71V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000284719
Start	174123261:174123261(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.647A>G
AA Mutation	p.Lys216Arg(p.K216R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000284719
Start	174079006:174079006(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1051G>A
AA Mutation	p.Glu351Lys(p.E351K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000284719
Start	174246802:174246802(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.14delA
AA Mutation	p.Lys5ArgfsTer19(p.K5Rfs*19)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	stop_gained
Transcription ID	ENST00000284719
Start	174078994:174078994(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1063G>T
AA Mutation	p.Glu355Ter(p.E355*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> OLA1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000284719
Start	174081199:174081199(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.919T>C
AA Mutation	p.Tyr307His(p.Y307H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript