Colon Cancer: Gene >> TNFRSF1B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000376259
Start	12188860:12188860(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.143A>G
AA Mutation	p.Gln48Arg(p.Q48R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000376259
Start	12192991:12192991(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764190618
CDS Mutation	c.680C>T
AA Mutation	p.Thr227Met(p.T227M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000376259
Start	12193971:12193971(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.804G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000376259
Start	12193094:12193094(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.783A>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000376259
Start	12207005:12207005(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1371G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> TNFRSF1B

Mutation ID	1
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000376259
Start	12193954:12193954(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.788-1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript