Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> FGF19

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000294312
Start	69703325:69703325(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.272C>T
AA Mutation	p.Ala91Val(p.A91V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000294312
Start	69699374:69699374(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.539G>T
AA Mutation	p.Arg180Met(p.R180M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000294312
Start	69703330:69703330(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.267C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> FGF19

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000294312
Start	69699349:69699349(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.564C>A
AA Mutation	p.Phe188Leu(p.F188L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000294312
Start	69699505:69699505(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769423572
CDS Mutation	c.408C>T
Mutation Classification	Silent
Feature Type	Transcript