Colon Cancer: Gene >> RNPEP

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000295640
Start	201999980:201999980(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1169A>C
AA Mutation	p.Asn390Thr(p.N390T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000295640
Start	201997510:201997510(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144833089
CDS Mutation	c.1046G>A
AA Mutation	p.Gly349Asp(p.G349D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000295640
Start	201999932:201999932(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140175504
CDS Mutation	c.1121C>T
AA Mutation	p.Thr374Met(p.T374M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000295640
Start	201997474:201997474(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1010C>T
AA Mutation	p.Thr337Ile(p.T337I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	inframe_insertion
Transcription ID	ENST00000295640
Start	201997373:201997374(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.909_910insAACAGA
AA Mutation	p.Pro303_Cys304insAsnArg(p.P303_C304insNR)
Mutation Classification	In_Frame_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> RNPEP

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000295640
Start	201997324:201997324(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.860A>G
AA Mutation	p.Asp287Gly(p.D287G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript