Colon Cancer: Gene >> DERL1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000259512
Start	123021451:123021451(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.502G>T
AA Mutation	p.Gly168Cys(p.G168C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000259512
Start	123030682:123030682(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.188C>A
AA Mutation	p.Pro63His(p.P63H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000259512
Start	123030659:123030659(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.211C>A
AA Mutation	p.Leu71Ile(p.L71I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000259512
Start	123023730:123023730(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.340T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000259512
Start	123015475:123015475(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.728delG
AA Mutation	p.Gly243AlafsTer31(p.G243Afs*31)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> DERL1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000259512
Start	123022722:123022722(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.415G>T
AA Mutation	p.Asp139Tyr(p.D139Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript