Colon Cancer: Gene >> BRCC3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000369462
Start	155120009:155120009(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.810G>T
AA Mutation	p.Lys270Asn(p.K270N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000369462
Start	155073415:155073415(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781808889
CDS Mutation	c.179G>A
AA Mutation	p.Arg60His(p.R60H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369462
Start	155099327:155099327(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.561T>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369462
Start	155071536:155071536(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782035489
CDS Mutation	c.9G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> BRCC3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000369462
Start	155120134:155120134(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.935T>A
AA Mutation	p.Leu312His(p.L312H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000369462
Start	155072345:155072345(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.140+2T>C
Mutation Classification	Splice_Site
Feature Type	Transcript