Colon Cancer: Gene >> EIF2S2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000374980
Start	34103522:34103522(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.237G>T
AA Mutation	p.Lys79Asn(p.K79N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000374980
Start	34096770:34096770(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.570G>T
AA Mutation	p.Lys190Asn(p.K190N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374980
Start	34112102:34112102(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.9G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	stop_gained
Transcription ID	ENST00000374980
Start	34105443:34105443(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.118G>T
AA Mutation	p.Glu40Ter(p.E40*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> EIF2S2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000374980
Start	34096695:34096695(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.645G>T
AA Mutation	p.Lys215Asn(p.K215N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript