Colon Cancer: Gene >> RAET1G

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000367360
Start	149917063:149917063(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.854C>T
AA Mutation	p.Ala285Val(p.A285V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000367360
Start	149919076:149919076(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.598G>T
AA Mutation	p.Gly200Cys(p.G200C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367360
Start	149916992:149916992(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.925T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	stop_gained
Transcription ID	ENST00000367360
Start	149919100:149919100(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.574G>T
AA Mutation	p.Gly192Ter(p.G192*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> RAET1G

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000367360
Start	149916916:149916916(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1001C>A
AA Mutation	p.Ser334Tyr(p.S334Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000367360
Start	149919162:149919162(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.512A>G
AA Mutation	p.Lys171Arg(p.K171R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367360
Start	149917005:149917005(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs560309852
CDS Mutation	c.912C>T
Mutation Classification	Silent
Feature Type	Transcript