Colon Cancer: Gene >> MAPRE1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000375571
Start	32848697:32848697(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.776G>A
AA Mutation	p.Gly259Glu(p.G259E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000375571
Start	32833852:32833852(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.257G>A
AA Mutation	p.Gly86Asp(p.G86D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000375571
Start	32846674:32846674(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762741175
CDS Mutation	c.654C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000375571
Start	32826032:32826032(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs565248642
CDS Mutation	c.105C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000375571
Start	32848696:32848696(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.779delG
AA Mutation	p.Gly260AlafsTer28(p.G260Afs*28)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> MAPRE1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000375571
Start	32826020:32826020(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.93T>G
AA Mutation	p.Asn31Lys(p.N31K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript