Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> BATF

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000286639
Start	75525129:75525129(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.109C>T
AA Mutation	p.Arg37Cys(p.R37C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000286639
Start	75546655:75546655(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772105665
CDS Mutation	c.362C>T
AA Mutation	p.Pro121Leu(p.P121L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000286639
Start	75546593:75546593(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.300G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000286639
Start	75546626:75546626(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748110657
CDS Mutation	c.333C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> BATF

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000286639
Start	75525129:75525129(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.109C>T
AA Mutation	p.Arg37Cys(p.R37C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript