Colon Cancer: Gene >> FGF20

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000180166
Start	16993266:16993266(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.442T>C
AA Mutation	p.Tyr148His(p.Y148H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000180166
Start	17001773:17001773(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.260G>A
AA Mutation	p.Gly87Asp(p.G87D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000180166
Start	17001942:17001942(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.91G>A
AA Mutation	p.Gly31Arg(p.G31R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000180166
Start	16993273:16993273(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.435G>T
AA Mutation	p.Glu145Asp(p.E145D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000180166
Start	16993083:16993083(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.625A>T
AA Mutation	p.Met209Leu(p.M209L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000180166
Start	17001952:17001952(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.81G>T
AA Mutation	p.Leu27Phe(p.L27F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000180166
Start	17001929:17001929(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.104C>T
AA Mutation	p.Pro35Leu(p.P35L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000180166
Start	17001937:17001937(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.96G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> FGF20

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000180166
Start	16995698:16995698(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.347G>T
AA Mutation	p.Gly116Val(p.G116V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000180166
Start	16993302:16993302(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201317229
CDS Mutation	c.406G>A
AA Mutation	p.Glu136Lys(p.E136K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript