Colon Cancer: Gene >> FGF7

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000267843
Start	49424466:49424466(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.169G>T
AA Mutation	p.Asp57Tyr(p.D57Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000267843
Start	49424406:49424406(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.109C>G
AA Mutation	p.Pro37Ala(p.P37A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000267843
Start	49424375:49424375(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.78T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	stop_gained
Transcription ID	ENST00000267843
Start	49424511:49424511(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766338451
CDS Mutation	c.214C>T
AA Mutation	p.Arg72Ter(p.R72*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> FGF7

No Mutation Annotation!