Colon Cancer: Gene >> ATF4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000337304
Start	39522156:39522156(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.610A>G
AA Mutation	p.Ile204Val(p.I204V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000337304
Start	39521851:39521851(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.305T>C
AA Mutation	p.Ile102Thr(p.I102T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000337304
Start	39522163:39522163(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.617A>G
AA Mutation	p.Gln206Arg(p.Q206R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000337304
Start	39521987:39521987(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781776700
CDS Mutation	c.441T>C
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> ATF4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000337304
Start	39522277:39522277(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.731G>T
AA Mutation	p.Arg244Met(p.R244M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000337304
Start	39521832:39521832(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.286T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000337304
Start	39522393:39522393(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.853delA
AA Mutation	p.Met285TrpfsTer36(p.M285Wfs*36)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript