Colon Cancer: Gene >> AURKB

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000585124
Start	8207206:8207206(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.368G>A
AA Mutation	p.Arg123His(p.R123H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000585124
Start	8206585:8206585(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.592C>T
AA Mutation	p.His198Tyr(p.H198Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000585124
Start	8206751:8206751(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs55871613
CDS Mutation	c.536C>T
AA Mutation	p.Thr179Met(p.T179M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000585124
Start	8204876:8204876(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201709756
CDS Mutation	c.1030G>A
AA Mutation	p.Ala344Thr(p.A344T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000585124
Start	8207800:8207800(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780771169
CDS Mutation	c.89G>A
AA Mutation	p.Arg30Gln(p.R30Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000585124
Start	8205012:8205012(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768656332
CDS Mutation	c.894G>T
AA Mutation	p.Met298Ile(p.M298I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000585124
Start	8205333:8205333(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.744C>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> AURKB

Mutation ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000585124
Start	8207839:8207839(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.50C>T
AA Mutation	p.Ala17Val(p.A17V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript