Colon Cancer: Gene >> PRPS1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000372435
Start	107647626:107647626(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.725C>T
AA Mutation	p.Thr242Ile(p.T242I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000372435
Start	107639355:107639355(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371538576
CDS Mutation	c.183C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000372435
Start	107642464:107642464(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.504C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> PRPS1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000372435
Start	107645215:107645215(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.569C>A
AA Mutation	p.Ala190Asp(p.A190D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000372435
Start	107642405:107642405(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.445C>A
AA Mutation	p.Pro149Thr(p.P149T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript