Colon Cancer: Gene >> ATG3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000283290
Start	112548626:112548626(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.250C>T
AA Mutation	p.Arg84Trp(p.R84W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000283290
Start	112537760:112537760(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.641G>T
AA Mutation	p.Arg214Leu(p.R214L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000283290
Start	112536595:112536595(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.674A>G
AA Mutation	p.Gln225Arg(p.Q225R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> ATG3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000283290
Start	112537818:112537818(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.583T>G
AA Mutation	p.Leu195Val(p.L195V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000283290
Start	112541822:112541822(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.456A>C
Mutation Classification	Silent
Feature Type	Transcript