Colon Cancer: Gene >> ATG4B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000404914
Start	241654602:241654602(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752539092
CDS Mutation	c.340G>A
AA Mutation	p.Ala114Thr(p.A114T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000404914
Start	241651096:241651096(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.97T>C
AA Mutation	p.Tyr33His(p.Y33H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000404914
Start	241654627:241654627(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs745479816
CDS Mutation	c.365A>G
AA Mutation	p.Tyr122Cys(p.Y122C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000404914
Start	241670734:241670734(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.966C>A
AA Mutation	p.Phe322Leu(p.F322L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000404914
Start	241668218:241668218(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771274919
CDS Mutation	c.808G>A
AA Mutation	p.Val270Ile(p.V270I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000404914
Start	241668643:241668643(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs534411323
CDS Mutation	c.915G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000404914
Start	241651274:241651274(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.123G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000404914
Start	241651059:241651059(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.60T>C
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> ATG4B

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000404914
Start	241651274:241651274(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.123G>A
Mutation Classification	Silent
Feature Type	Transcript