Colon Cancer: Gene >> TERT

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000310581
Start	1278703:1278703(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2224C>T
AA Mutation	p.Arg742Cys(p.R742C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000310581
Start	1280267:1280267(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1841C>T
AA Mutation	p.Pro614Leu(p.P614L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000310581
Start	1293817:1293817(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1069G>A
AA Mutation	p.Ala357Thr(p.A357T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000310581
Start	1280158:1280158(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1950G>T
AA Mutation	p.Arg650Ser(p.R650S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000310581
Start	1293672:1293672(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1214A>G
AA Mutation	p.Tyr405Cys(p.Y405C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000310581
Start	1282479:1282479(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1719C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000310581
Start	1278665:1278665(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778622091
CDS Mutation	c.2262C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000310581
Start	1272230:1272230(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747564177
CDS Mutation	c.2337C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> TERT

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000310581
Start	1253798:1253798(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199422306
CDS Mutation	c.3329C>T
AA Mutation	p.Thr1110Met(p.T1110M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000310581
Start	1264454:1264454(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764925909
CDS Mutation	c.2793C>T
Mutation Classification	Silent
Feature Type	Transcript