Colon Cancer: Gene >> CPM

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000338356
Start	68867015:68867015(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.821A>G
AA Mutation	p.Gln274Arg(p.Q274R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000338356
Start	68866971:68866971(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs538250941
CDS Mutation	c.865C>T
AA Mutation	p.Arg289Cys(p.R289C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000338356
Start	68870249:68870249(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759455218
CDS Mutation	c.582C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> CPM

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000338356
Start	68856564:68856564(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1205C>A
AA Mutation	p.Ser402Tyr(p.S402Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000338356
Start	68870370:68870370(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200496918
CDS Mutation	c.461G>A
AA Mutation	p.Arg154Gln(p.R154Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000338356
Start	68856559:68856559(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1210C>T
AA Mutation	p.Pro404Ser(p.P404S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000338356
Start	68869457:68869457(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.655G>T
AA Mutation	p.Asp219Tyr(p.D219Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript