Colon Cancer: Gene >> TOB2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000327492
Start	41437134:41437134(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.212C>T
AA Mutation	p.Ala71Val(p.A71V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000327492
Start	41436468:41436468(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.878C>T
AA Mutation	p.Thr293Ile(p.T293I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000327492
Start	41436455:41436455(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.891C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000327492
Start	41436521:41436521(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376866752
CDS Mutation	c.825C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> TOB2

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000327492
Start	41436755:41436755(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.591A>G
Mutation Classification	Silent
Feature Type	Transcript