Colon Cancer: Gene >> NGB

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000298352
Start	77266575:77266575(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775492814
CDS Mutation	c.417C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	stop_gained
Transcription ID	ENST00000298352
Start	77266556:77266556(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.436C>T
AA Mutation	p.Arg146Ter(p.R146*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> NGB

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000298352
Start	77269312:77269312(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.104A>G
AA Mutation	p.Glu35Gly(p.E35G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000298352
Start	77269291:77269291(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.125T>C
AA Mutation	p.Phe42Ser(p.F42S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000298352
Start	77268585:77268585(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.202G>A
AA Mutation	p.Val68Met(p.V68M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000298352
Start	77268526:77268526(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.261G>T
AA Mutation	p.Glu87Asp(p.E87D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript