Colon Cancer: Gene >> VPS35

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000299138
Start	46682095:46682095(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.183G>T
AA Mutation	p.Lys61Asn(p.K61N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000299138
Start	46678987:46678987(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.676C>T
AA Mutation	p.Arg226Cys(p.R226C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000299138
Start	46683595:46683595(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.15G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000299138
Start	46676642:46676642(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.855C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	stop_gained
Transcription ID	ENST00000299138
Start	46679032:46679032(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.631C>T
AA Mutation	p.Arg211Ter(p.R211*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> VPS35

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000299138
Start	46679076:46679076(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.587G>A
AA Mutation	p.Arg196Gln(p.R196Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000299138
Start	46681414:46681414(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.286G>A
AA Mutation	p.Glu96Lys(p.E96K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript