Colon Cancer: Gene >> ATF1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000262053
Start	50780210:50780210(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763994606
CDS Mutation	c.65G>A
AA Mutation	p.Gly22Glu(p.G22E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000262053
Start	50780171:50780171(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.26C>T
AA Mutation	p.Thr9Met(p.T9M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000262053
Start	50795951:50795951(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.136G>A
AA Mutation	p.Asp46Asn(p.D46N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262053
Start	50814104:50814104(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.423T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000262053
Start	50819740:50819740(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.781delA
AA Mutation	p.Thr261LeufsTer2(p.T261Lfs*2)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> ATF1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000262053
Start	50780233:50780233(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.88C>A
AA Mutation	p.Gln30Lys(p.Q30K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript