Colon Cancer: Gene >> CCNB1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000256442
Start	69177254:69177254(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1099C>T
AA Mutation	p.His367Tyr(p.H367Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000256442
Start	69171277:69171277(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.371C>G
AA Mutation	p.Thr124Ser(p.T124S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000256442
Start	69175499:69175499(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1045T>G
AA Mutation	p.Phe349Val(p.F349V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000256442
Start	69171355:69171355(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.449T>C
AA Mutation	p.Ile150Thr(p.I150T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000256442
Start	69174975:69174975(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.804C>G
AA Mutation	p.Asp268Glu(p.D268E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000256442
Start	69174986:69174986(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.815T>G
AA Mutation	p.Val272Gly(p.V272G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000256442
Start	69174956:69174956(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.785A>G
AA Mutation	p.Tyr262Cys(p.Y262C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> CCNB1

No Mutation Annotation!