Colon Cancer: Gene >> OXCT1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000196371
Start	41870289:41870289(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.70T>C
AA Mutation	p.Trp24Arg(p.W24R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000196371
Start	41805668:41805668(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766119402
CDS Mutation	c.854G>A
AA Mutation	p.Arg285Gln(p.R285Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000196371
Start	41762195:41762195(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1254G>C
AA Mutation	p.Lys418Asn(p.K418N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000196371
Start	41762167:41762167(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1282G>T
AA Mutation	p.Asp428Tyr(p.D428Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000196371
Start	41731737:41731737(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs180683984
CDS Mutation	c.1555G>A
AA Mutation	p.Ala519Thr(p.A519T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> OXCT1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000196371
Start	41807378:41807378(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.793T>G
AA Mutation	p.Tyr265Asp(p.Y265D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000196371
Start	41850158:41850158(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.436C>T
AA Mutation	p.Arg146Cys(p.R146C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000196371
Start	41850150:41850150(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372032720
CDS Mutation	c.444C>T
Mutation Classification	Silent
Feature Type	Transcript