Colon Cancer: Gene >> CDK5R1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000313401
Start	32487691:32487691(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.71T>C
AA Mutation	p.Val24Ala(p.V24A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000313401
Start	32488281:32488281(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.661G>A
AA Mutation	p.Glu221Lys(p.E221K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000313401
Start	32487949:32487949(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.329C>A
AA Mutation	p.Pro110Gln(p.P110Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000313401
Start	32488156:32488156(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.536G>A
AA Mutation	p.Arg179His(p.R179H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000313401
Start	32487729:32487729(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.109A>C
AA Mutation	p.Lys37Gln(p.K37Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000313401
Start	32487908:32487908(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.288C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000313401
Start	32487857:32487857(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.237G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> CDK5R1

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000313401
Start	32488518:32488518(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.898C>A
Mutation Classification	Silent
Feature Type	Transcript