Colon Cancer: Gene >> ATF7

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000548446
Start	53517316:53517316(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1306G>A
AA Mutation	p.Ala436Thr(p.A436T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000548446
Start	53534578:53534578(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.517T>A
AA Mutation	p.Tyr173Asn(p.Y173N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000548446
Start	53524646:53524646(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1076G>A
AA Mutation	p.Arg359His(p.R359H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000548446
Start	53533173:53533173(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.680C>T
AA Mutation	p.Pro227Leu(p.P227L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000548446
Start	53517179:53517179(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372771818
CDS Mutation	c.1443G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000548446
Start	53543303:53543303(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs769377214
CDS Mutation	c.291delA
AA Mutation	p.Lys97AsnfsTer29(p.K97Nfs*29)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000548446
Start	53533190:53533190(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.663delG
AA Mutation	p.Pro222LeufsTer48(p.P222Lfs*48)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	stop_gained
Transcription ID	ENST00000548446
Start	53524632:53524632(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1090C>T
AA Mutation	p.Arg364Ter(p.R364*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000548446
Start	53524725:53524726(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.996dupG
AA Mutation	p.Arg333AlafsTer8(p.R333Afs*8)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> ATF7

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000548446
Start	53537424:53537424(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.426G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000548446
Start	53517170:53517170(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1452C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000548446
Start	53600992:53600992(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs377276777
CDS Mutation	c.9C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	stop_gained
Transcription ID	ENST00000548446
Start	53524593:53524593(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1129G>T
AA Mutation	p.Glu377Ter(p.E377*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript