Colon Cancer: Gene >> CENPB

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000379751
Start	3786189:3786189(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.295A>G
AA Mutation	p.Ile99Val(p.I99V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000379751
Start	3786173:3786173(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.311C>T
AA Mutation	p.Ala104Val(p.A104V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000379751
Start	3785615:3785615(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.869G>A
AA Mutation	p.Arg290His(p.R290H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000379751
Start	3785242:3785242(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1242A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000379751
Start	3784933:3784933(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756348140
CDS Mutation	c.1551G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000379751
Start	3785172:3785172(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs772292203
CDS Mutation	c.1312delG
AA Mutation	p.Glu438LysfsTer43(p.E438Kfs*43)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> CENPB

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000379751
Start	3785354:3785354(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1130C>T
AA Mutation	p.Pro377Leu(p.P377L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000379751
Start	3784899:3784899(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765081320
CDS Mutation	c.1585G>A
AA Mutation	p.Asp529Asn(p.D529N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript