Colon Cancer: Gene >> BUB3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000368865
Start	123160495:123160495(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.506A>G
AA Mutation	p.Tyr169Cys(p.Y169C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000368865
Start	123160537:123160537(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.548G>A
AA Mutation	p.Arg183His(p.R183H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000368865
Start	123160522:123160522(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767340055
CDS Mutation	c.533T>C
AA Mutation	p.Leu178Pro(p.L178P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000368865
Start	123162658:123162658(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.801G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000368865
Start	123157864:123157865(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.405_406delTC
AA Mutation	p.Gln136AlafsTer2(p.Q136Afs*2)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000368865
Start	123162349:123162350(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.690_691insGGTAA
AA Mutation	p.Ile231GlyfsTer30(p.I231Gfs*30)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> BUB3

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000368865
Start	123162355:123162355(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.696G>A
Mutation Classification	Silent
Feature Type	Transcript