Colon Cancer: Gene >> FGF17

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000359441
Start	22046202:22046202(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.161A>G
AA Mutation	p.Glu54Gly(p.E54G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000359441
Start	22048239:22048239(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.641C>A
AA Mutation	p.Pro214His(p.P214H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000359441
Start	22048245:22048245(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.647C>T
AA Mutation	p.Thr216Met(p.T216M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000359441
Start	22048128:22048128(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs398123025
CDS Mutation	c.530G>A
AA Mutation	p.Arg177His(p.R177H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359441
Start	22046251:22046251(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373182132
CDS Mutation	c.210G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> FGF17

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000359441
Start	22046568:22046568(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.292C>T
AA Mutation	p.Arg98Cys(p.R98C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359441
Start	22046128:22046128(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs552877908
CDS Mutation	c.87G>A
Mutation Classification	Silent
Feature Type	Transcript