Colon Cancer: Gene >> CA11

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000084798
Start	48639016:48639016(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.833C>T
AA Mutation	p.Ser278Phe(p.S278F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000084798
Start	48639591:48639591(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.598C>T
AA Mutation	p.Arg200Cys(p.R200C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000084798
Start	48638972:48638972(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.877C>T
AA Mutation	p.Pro293Ser(p.P293S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000084798
Start	48638998:48638998(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.851T>C
AA Mutation	p.Leu284Pro(p.L284P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000084798
Start	48645615:48645615(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.18T>C
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> CA11

No Mutation Annotation!