Colon Cancer: Gene >> ATF5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000423777
Start	49932635:49932635(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.392C>T
AA Mutation	p.Pro131Leu(p.P131L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000423777
Start	49932494:49932494(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.251C>T
AA Mutation	p.Pro84Leu(p.P84L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000423777
Start	49930923:49930923(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs745985003
CDS Mutation	c.73G>A
AA Mutation	p.Val25Ile(p.V25I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000423777
Start	49932524:49932524(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.281C>A
AA Mutation	p.Thr94Asn(p.T94N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000423777
Start	49932987:49932987(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373471926
CDS Mutation	c.744C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000423777
Start	49930954:49930954(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs768611141
CDS Mutation	c.109delC
AA Mutation	p.Leu37TrpfsTer31(p.L37Wfs*31)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000423777
Start	49932493:49932493(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.255delC
AA Mutation	p.Gly86AlafsTer32(p.G86Afs*32)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000423777
Start	49931009:49931009(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.164delG
AA Mutation	p.Gly55GlufsTer13(p.G55Efs*13)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> ATF5

No Mutation Annotation!