Colon Cancer: Gene >> CTBP1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000290921
Start	1228213:1228213(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.326C>T
AA Mutation	p.Ser109Leu(p.S109L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000290921
Start	1212947:1212947(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138269585
CDS Mutation	c.1105G>A
AA Mutation	p.Val369Ile(p.V369I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000290921
Start	1238212:1238212(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773926313
CDS Mutation	c.166G>A
AA Mutation	p.Ala56Thr(p.A56T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000290921
Start	1214452:1214452(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.784G>A
AA Mutation	p.Val262Met(p.V262M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000290921
Start	1216116:1216116(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764862588
CDS Mutation	c.637C>T
AA Mutation	p.Arg213Trp(p.R213W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000290921
Start	1238230:1238230(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.148A>G
AA Mutation	p.Thr50Ala(p.T50A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000290921
Start	1213005:1213005(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1047C>G
AA Mutation	p.Asn349Lys(p.N349K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000290921
Start	1214440:1214440(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.796C>T
AA Mutation	p.Arg266Trp(p.R266W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000290921
Start	1212306:1212306(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1257C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000290921
Start	1225433:1225433(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.474C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> CTBP1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000290921
Start	1228250:1228250(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.289C>T
AA Mutation	p.Arg97Trp(p.R97W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript