Colon Cancer: Gene >> ATP6AP2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000378438
Start	40589100:40589100(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.152G>C
AA Mutation	p.Gly51Ala(p.G51A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000378438
Start	40589081:40589081(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.133G>A
AA Mutation	p.Val45Met(p.V45M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000378438
Start	40600762:40600762(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.739T>C
AA Mutation	p.Phe247Leu(p.F247L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000378438
Start	40597536:40597536(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.406A>G
AA Mutation	p.Met136Val(p.M136V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	stop_gained
Transcription ID	ENST00000378438
Start	40605744:40605744(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1042C>T
AA Mutation	p.Arg348Ter(p.R348*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	stop_gained
Transcription ID	ENST00000378438
Start	40599681:40599681(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.678T>G
AA Mutation	p.Tyr226Ter(p.Y226*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> ATP6AP2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000378438
Start	40605745:40605745(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1043G>A
AA Mutation	p.Arg348Gln(p.R348Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	stop_gained
Transcription ID	ENST00000378438
Start	40605744:40605744(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1042C>T
AA Mutation	p.Arg348Ter(p.R348*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript