Colon Cancer: Gene >> BCAT2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000316273
Start	48795447:48795447(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1158C>G
AA Mutation	p.His386Gln(p.H386Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000316273
Start	48800066:48800066(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs549092161
CDS Mutation	c.446G>A
AA Mutation	p.Arg149His(p.R149H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000316273
Start	48811001:48811001(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.7G>A
AA Mutation	p.Ala3Thr(p.A3T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000316273
Start	48796452:48796452(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1116C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000316273
Start	48799779:48799779(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.591G>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> BCAT2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000316273
Start	48800031:48800031(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.481G>A
AA Mutation	p.Asp161Asn(p.D161N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000316273
Start	48806581:48806581(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.236G>A
AA Mutation	p.Arg79Gln(p.R79Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript