Colon Cancer: Gene >> GREM1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000622074
Start	32731151:32731151(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.461T>C
AA Mutation	p.Val154Ala(p.V154A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000622074
Start	32730858:32730858(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.168G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000622074
Start	32730789:32730789(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.104delC
AA Mutation	p.Pro35ArgfsTer49(p.P35Rfs*49)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> GREM1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000622074
Start	32731036:32731036(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.346C>A
AA Mutation	p.Arg116Ser(p.R116S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000622074
Start	32731037:32731037(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756849803
CDS Mutation	c.347G>A
AA Mutation	p.Arg116His(p.R116H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript