Colon Cancer: Gene >> CERS5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000317551
Start	50137817:50137817(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.547C>A
AA Mutation	p.Leu183Ile(p.L183I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000317551
Start	50143119:50143119(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.389G>T
AA Mutation	p.Arg130Met(p.R130M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000317551
Start	50130679:50130679(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373121500
CDS Mutation	c.1045C>T
AA Mutation	p.Arg349Cys(p.R349C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000317551
Start	50144031:50144031(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.224G>A
AA Mutation	p.Cys75Tyr(p.C75Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000317551
Start	50138588:50138588(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.522C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> CERS5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000317551
Start	50130550:50130550(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1174G>A
AA Mutation	p.Glu392Lys(p.E392K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000317551
Start	50143128:50143128(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs547919626
CDS Mutation	c.380G>A
AA Mutation	p.Arg127His(p.R127H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript