Colon Cancer: Gene >> RAB33B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000305626
Start	139454394:139454394(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.199G>T
AA Mutation	p.Gly67Trp(p.G67W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000305626
Start	139473057:139473057(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.621T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000305626
Start	139472772:139472772(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs142541603
CDS Mutation	c.336C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> RAB33B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000305626
Start	139473056:139473056(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.620T>G
AA Mutation	p.Leu207Arg(p.L207R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000305626
Start	139472816:139472816(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.380C>A
AA Mutation	p.Ser127Tyr(p.S127Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript