Colon Cancer: Gene >> RAET1E

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000357183
Start	149889473:149889473(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.497A>C
AA Mutation	p.Lys166Thr(p.K166T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000357183
Start	149889567:149889567(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.403G>A
AA Mutation	p.Gly135Ser(p.G135S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000357183
Start	149890053:149890053(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs149529086
CDS Mutation	c.178C>A
AA Mutation	p.Leu60Ile(p.L60I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000357183
Start	149890075:149890075(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs147219649
CDS Mutation	c.156G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	stop_gained
Transcription ID	ENST00000357183
Start	149888531:149888531(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.759G>A
AA Mutation	p.Trp253Ter(p.W253*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> RAET1E

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000357183
Start	149889492:149889492(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.478A>C
AA Mutation	p.Ile160Leu(p.I160L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000357183
Start	149889442:149889442(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775664164
CDS Mutation	c.528G>A
Mutation Classification	Silent
Feature Type	Transcript