Colon Cancer: Gene >> NCR2

Mutation ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000373089
Start	41350678:41350678(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.645G>T
AA Mutation	p.Trp215Cys(p.W215C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000373089
Start	41350780:41350780(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.747T>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000373089
Start	41350759:41350759(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.726G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> NCR2

No Mutation Annotation!