Colon Cancer: Gene >> CTRL

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000574481
Start	67930002:67930002(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144794688
CDS Mutation	c.727G>A
AA Mutation	p.Ala243Thr(p.A243T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000574481
Start	67930079:67930079(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.650C>A
AA Mutation	p.Pro217His(p.P217H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000574481
Start	67930256:67930256(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.562C>T
AA Mutation	p.Arg188Trp(p.R188W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000574481
Start	67930003:67930003(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs542410288
CDS Mutation	c.726C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000574481
Start	67930087:67930087(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140705263
CDS Mutation	c.642C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000574481
Start	67930526:67930526(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.381C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> CTRL

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000574481
Start	67930734:67930734(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200180034
CDS Mutation	c.310G>A
AA Mutation	p.Val104Ile(p.V104I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript