Colon Cancer: Gene >> NMS

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000376865
Start	100472798:100472798(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.80T>G
AA Mutation	p.Phe27Cys(p.F27C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000376865
Start	100479353:100479353(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.262T>G
AA Mutation	p.Phe88Val(p.F88V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000376865
Start	100470514:100470514(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.26C>T
AA Mutation	p.Pro9Leu(p.P9L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> NMS

No Mutation Annotation!