Colon Cancer: Gene >> RALA

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000005257
Start	39696695:39696695(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.334T>G
AA Mutation	p.Leu112Val(p.L112V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000005257
Start	39686729:39686729(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.62G>C
AA Mutation	p.Gly21Ala(p.G21A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000005257
Start	39690464:39690464(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.197T>A
AA Mutation	p.Ile66Asn(p.I66N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	stop_gained
Transcription ID	ENST00000005257
Start	39706150:39706150(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.526C>T
AA Mutation	p.Arg176Ter(p.R176*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> RALA

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000005257
Start	39706152:39706152(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.528A>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	stop_gained
Transcription ID	ENST00000005257
Start	39706150:39706150(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.526C>T
AA Mutation	p.Arg176Ter(p.R176*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript