Colon Cancer: Gene >> CDK5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000485972
Start	151056953:151056953(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.149G>A
AA Mutation	p.Arg50Gln(p.R50Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000485972
Start	151057818:151057818(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.31G>T
AA Mutation	p.Gly11Trp(p.G11W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000485972
Start	151054043:151054043(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.845A>G
AA Mutation	p.Gln282Arg(p.Q282R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000485972
Start	151056621:151056621(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.271T>G
AA Mutation	p.Phe91Val(p.F91V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000485972
Start	151055369:151055369(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.488T>G
AA Mutation	p.Val163Gly(p.V163G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000485972
Start	151055077:151055077(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.600G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> CDK5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000485972
Start	151055078:151055078(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.599G>A
AA Mutation	p.Arg200Gln(p.R200Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript