Colon Cancer: Gene >> TOR1A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000351698
Start	129814108:129814108(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs727502811
CDS Mutation	c.863G>A
AA Mutation	p.Arg288Gln(p.R288Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000351698
Start	129813980:129813980(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs147805267
CDS Mutation	c.991G>A
AA Mutation	p.Asp331Asn(p.D331N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000351698
Start	129818812:129818812(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.553C>T
AA Mutation	p.Pro185Ser(p.P185S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000351698
Start	129818593:129818593(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.675A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000351698
Start	129814209:129814209(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.762C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000351698
Start	129822626:129822626(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760826255
CDS Mutation	c.399G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> TOR1A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000351698
Start	129814196:129814196(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.775G>A
AA Mutation	p.Asp259Asn(p.D259N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	stop_gained
Transcription ID	ENST00000351698
Start	129818899:129818899(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.466C>T
AA Mutation	p.Arg156Ter(p.R156*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript