Colon Cancer: Gene >> CHMP2A

Mutation ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000312547
Start	58551908:58551908(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144804005
CDS Mutation	c.539C>T
AA Mutation	p.Ser180Leu(p.S180L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000312547
Start	58552318:58552318(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.289A>G
AA Mutation	p.Asn97Asp(p.N97D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000312547
Start	58552387:58552387(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376979258
CDS Mutation	c.220C>T
AA Mutation	p.Arg74Cys(p.R74C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000312547
Start	58554120:58554120(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.93C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> CHMP2A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000312547
Start	58554061:58554061(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.152C>T
AA Mutation	p.Ala51Val(p.A51V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript