Colon Cancer: Gene >> MAGT1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000618282
Start	77830845:77830845(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.952C>T
AA Mutation	p.Leu318Phe(p.L318F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000618282
Start	77875532:77875532(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.168G>T
AA Mutation	p.Met56Ile(p.M56I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000618282
Start	77855565:77855565(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.698G>A
AA Mutation	p.Gly233Asp(p.G233D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000618282
Start	77856788:77856788(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.617G>A
AA Mutation	p.Arg206Gln(p.R206Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	stop_gained;splice_region_variant
Transcription ID	ENST00000618282
Start	77830807:77830807(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.990C>A
AA Mutation	p.Tyr330Ter(p.Y330*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> MAGT1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000618282
Start	77857481:77857481(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.407C>T
AA Mutation	p.Ala136Val(p.A136V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript