Colon Cancer: Gene >> ATF2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000264110
Start	175074760:175074760(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs147478928
CDS Mutation	c.1367C>T
AA Mutation	p.Ser456Leu(p.S456L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000264110
Start	175097476:175097476(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773144879
CDS Mutation	c.946C>A
AA Mutation	p.Gln316Lys(p.Q316K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000264110
Start	175111624:175111624(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.772G>T
AA Mutation	p.Val258Phe(p.V258F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000264110
Start	175093061:175093061(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1185G>T
AA Mutation	p.Gln395His(p.Q395H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000264110
Start	175080720:175080720(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1231C>T
AA Mutation	p.Leu411Phe(p.L411F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000264110
Start	175097487:175097487(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767222965
CDS Mutation	c.935C>T
AA Mutation	p.Pro312Leu(p.P312L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264110
Start	175074729:175074729(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1398C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264110
Start	175121511:175121511(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.132C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant;splice_region_variant
Transcription ID	ENST00000264110
Start	175118251:175118251(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.318delA
AA Mutation	p.Met107CysfsTer3(p.M107Cfs*3)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> ATF2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000264110
Start	175093198:175093198(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1048G>T
AA Mutation	p.Asp350Tyr(p.D350Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript