Colon Cancer: Gene >> SP2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000376741
Start	47916600:47916600(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.529G>A
AA Mutation	p.Val177Ile(p.V177I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000376741
Start	47916472:47916472(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.401C>T
AA Mutation	p.Ala134Val(p.A134V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000376741
Start	47925511:47925511(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1711G>A
AA Mutation	p.Glu571Lys(p.E571K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000376741
Start	47925050:47925050(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1504C>T
AA Mutation	p.Arg502Cys(p.R502C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000376741
Start	47916650:47916650(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764970167
CDS Mutation	c.579C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	stop_gained
Transcription ID	ENST00000376741
Start	47923121:47923121(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1219C>T
AA Mutation	p.Arg407Ter(p.R407*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> SP2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000376741
Start	47916202:47916202(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.131A>C
AA Mutation	p.Lys44Thr(p.K44T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript