Colon Cancer: Gene >> EIF5AL1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000520547
Start	79512852:79512852(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.203A>C
AA Mutation	p.Lys68Thr(p.K68T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000520547
Start	79512808:79512808(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.159C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000520547
Start	79512787:79512787(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.138G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000520547
Start	79512670:79512670(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.21C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000520547
Start	79512868:79512868(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.219C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000520547
Start	79512986:79512987(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.338dupG
AA Mutation	p.Leu114SerfsTer3(p.L114Sfs*3)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> EIF5AL1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000520547
Start	79512963:79512963(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.314G>A
AA Mutation	p.Ser105Asn(p.S105N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript