Colon Cancer: Gene >> CTBP2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000337195
Start	124998000:124998000(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.529C>T
AA Mutation	p.Arg177Cys(p.R177C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000337195
Start	124992734:124992734(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1118A>C
AA Mutation	p.Gln373Pro(p.Q373P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000337195
Start	124998080:124998080(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771702203
CDS Mutation	c.449C>T
AA Mutation	p.Thr150Met(p.T150M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000337195
Start	125002970:125002970(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148802158
CDS Mutation	c.348C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000337195
Start	125002988:125002988(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.330C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000337195
Start	125039004:125039004(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.51T>C
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> CTBP2

No Mutation Annotation!