Colon Cancer: Gene >> FGF18

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000274625
Start	171449248:171449248(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.352G>T
AA Mutation	p.Gly118Trp(p.G118W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000274625
Start	171436250:171436250(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775534638
CDS Mutation	c.227G>A
AA Mutation	p.Arg76His(p.R76H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000274625
Start	171436123:171436123(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.100C>T
AA Mutation	p.Arg34Cys(p.R34C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000274625
Start	171436091:171436091(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.70-2A>G
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> FGF18

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000274625
Start	171456599:171456599(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.418G>A
AA Mutation	p.Ala140Thr(p.A140T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000274625
Start	171436251:171436251(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760722261
CDS Mutation	c.228C>T
Mutation Classification	Silent
Feature Type	Transcript