Colon Cancer: Gene >> APOBEC3F

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000308521
Start	39045439:39045439(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.463T>C
AA Mutation	p.Cys155Arg(p.C155R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000308521
Start	39045131:39045131(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774288237
CDS Mutation	c.362G>A
AA Mutation	p.Arg121His(p.R121H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000308521
Start	39045073:39045073(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.304A>G
AA Mutation	p.Lys102Glu(p.K102E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000308521
Start	39049501:39049501(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761754118
CDS Mutation	c.643G>A
AA Mutation	p.Glu215Lys(p.E215K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000308521
Start	39043078:39043078(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.159C>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> APOBEC3F

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000308521
Start	39049495:39049495(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs745372879
CDS Mutation	c.637C>T
AA Mutation	p.Arg213Trp(p.R213W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript