Colon Cancer: Gene >> CBR1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000290349
Start	36072452:36072452(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.404T>C
AA Mutation	p.Val135Ala(p.V135A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000290349
Start	36072704:36072704(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.656A>G
AA Mutation	p.Asp219Gly(p.D219G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000290349
Start	36072616:36072616(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.568C>T
AA Mutation	p.Pro190Ser(p.P190S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000290349
Start	36071026:36071026(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.366C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000290349
Start	36072815:36072815(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.770delT
AA Mutation	p.Leu257CysfsTer38(p.L257Cfs*38)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000290349
Start	36070343:36070343(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.229delC
AA Mutation	p.Leu77CysfsTer33(p.L77Cfs*33)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> CBR1

No Mutation Annotation!