Colon Cancer: Gene >> TTR

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000237014
Start	31595199:31595199(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.280G>T
AA Mutation	p.Asp94Tyr(p.D94Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000237014
Start	31591955:31591955(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.53C>T
AA Mutation	p.Ser18Phe(p.S18F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000237014
Start	31595135:31595135(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.216T>C
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> TTR

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000237014
Start	31595246:31595246(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.327G>T
AA Mutation	p.Glu109Asp(p.E109D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript