Colon Cancer: Gene >> MAGEA3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000370278
Start	152701622:152701622(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.790A>C
AA Mutation	p.Ser264Arg(p.S264R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000370278
Start	152701489:152701489(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.657G>T
AA Mutation	p.Glu219Asp(p.E219D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000370278
Start	152701509:152701509(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.677G>T
AA Mutation	p.Ser226Ile(p.S226I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000370278
Start	152701114:152701114(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.282G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000370278
Start	152701628:152701628(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.797delC
AA Mutation	p.Pro266LeufsTer19(p.P266Lfs*19)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> MAGEA3

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000370278
Start	152701348:152701348(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.516C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	stop_gained
Transcription ID	ENST00000370278
Start	152701466:152701466(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.634G>T
AA Mutation	p.Glu212Ter(p.E212*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript