Colon Cancer: Gene >> BTG4

Mutation ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000356018
Start	111495163:111495163(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.662G>T
AA Mutation	p.Arg221Ile(p.R221I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000356018
Start	111497344:111497344(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.377T>A
AA Mutation	p.Leu126Gln(p.L126Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000356018
Start	111498043:111498043(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764916472
CDS Mutation	c.266C>T
AA Mutation	p.Pro89Leu(p.P89L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356018
Start	111497373:111497373(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.348T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000356018
Start	111495298:111495299(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.526_527insCTCTG
AA Mutation	p.Gln176ProfsTer?(p.Q176Pfs*?)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> BTG4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000356018
Start	111497329:111497329(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.392G>T
AA Mutation	p.Ser131Ile(p.S131I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356018
Start	111495198:111495198(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.627T>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	stop_gained
Transcription ID	ENST00000356018
Start	111498683:111498683(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.94G>T
AA Mutation	p.Glu32Ter(p.E32*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript