Colon Cancer: Gene >> CKB

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000348956
Start	103520007:103520007(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1003G>A
AA Mutation	p.Asp335Asn(p.D335N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000348956
Start	103522364:103522364(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.130G>A
AA Mutation	p.Ala44Thr(p.A44T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000348956
Start	103520181:103520181(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.908G>A
AA Mutation	p.Gly303Asp(p.G303D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000348956
Start	103520216:103520216(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.873G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000348956
Start	103520204:103520204(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763930350
CDS Mutation	c.885G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> CKB

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000348956
Start	103522351:103522351(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.143C>G
AA Mutation	p.Pro48Arg(p.P48R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript