Colon Cancer: Gene >> RPIA

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000283646
Start	88735690:88735690(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.549G>T
AA Mutation	p.Lys183Asn(p.K183N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000283646
Start	88749989:88749989(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.847G>A
AA Mutation	p.Asp283Asn(p.D283N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000283646
Start	88735727:88735727(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.586G>A
AA Mutation	p.Ala196Thr(p.A196T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000283646
Start	88691899:88691899(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.201C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000283646
Start	88736643:88736643(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754790516
CDS Mutation	c.705C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> RPIA

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000283646
Start	88700046:88700046(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.384T>C
Mutation Classification	Silent
Feature Type	Transcript