Colon Cancer: Gene >> CAB39

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000258418
Start	230798775:230798775(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.445G>A
AA Mutation	p.Glu149Lys(p.E149K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000258418
Start	230790915:230790915(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.158T>G
AA Mutation	p.Ile53Ser(p.I53S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000258418
Start	230798850:230798850(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372860193
CDS Mutation	c.520G>A
AA Mutation	p.Glu174Lys(p.E174K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000258418
Start	230818611:230818611(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143207616
CDS Mutation	c.933C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> CAB39

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000258418
Start	230790917:230790917(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.160C>A
AA Mutation	p.Leu54Met(p.L54M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000258418
Start	230790925:230790925(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.168C>T
Mutation Classification	Silent
Feature Type	Transcript