Colon Cancer: Gene >> CCNB2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000288207
Start	59117265:59117265(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.872T>C
AA Mutation	p.Met291Thr(p.M291T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000288207
Start	59114769:59114769(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144432316
CDS Mutation	c.490C>T
AA Mutation	p.Arg164Cys(p.R164C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000288207
Start	59117340:59117340(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.947C>T
AA Mutation	p.Ser316Phe(p.S316F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000288207
Start	59124845:59124845(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1165G>A
AA Mutation	p.Asp389Asn(p.D389N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000288207
Start	59114775:59114775(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759811496
CDS Mutation	c.496C>T
AA Mutation	p.Arg166Cys(p.R166C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> CCNB2

No Mutation Annotation!