Colon Cancer: Gene >> BRAP

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000419234
Start	111681767:111681767(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.313G>T
AA Mutation	p.Asp105Tyr(p.D105Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000419234
Start	111672767:111672767(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.641C>T
AA Mutation	p.Ala214Val(p.A214V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000419234
Start	111650024:111650024(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1330A>C
AA Mutation	p.Lys444Gln(p.K444Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000419234
Start	111681724:111681724(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.356C>T
AA Mutation	p.Ser119Phe(p.S119F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000419234
Start	111683273:111683273(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764780095
CDS Mutation	c.117G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> BRAP

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000419234
Start	111655592:111655592(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1285C>T
AA Mutation	p.Arg429Trp(p.R429W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000419234
Start	111658760:111658760(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1197G>T
AA Mutation	p.Glu399Asp(p.E399D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript