Colon Cancer: Gene >> SNCB

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000310112
Start	176629599:176629599(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201389179
CDS Mutation	c.56C>T
AA Mutation	p.Ala19Val(p.A19V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000310112
Start	176629547:176629547(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775624759
CDS Mutation	c.108C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000310112
Start	176629613:176629613(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373426715
CDS Mutation	c.42C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> SNCB

No Mutation Annotation!