Colon Cancer: Gene >> EIF3L

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000624234
Start	37877839:37877839(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1243T>C
AA Mutation	p.Tyr415His(p.Y415H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000624234
Start	37886815:37886815(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1626C>A
AA Mutation	p.Phe542Leu(p.F542L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000624234
Start	37875943:37875943(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1009G>A
AA Mutation	p.Ala337Thr(p.A337T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000624234
Start	37858691:37858691(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.386T>C
AA Mutation	p.Leu129Pro(p.L129P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000624234
Start	37877685:37877685(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1089G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000624234
Start	37874503:37874503(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.885G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000624234
Start	37877707:37877707(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1111C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> EIF3L

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000624234
Start	37874510:37874510(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760820592
CDS Mutation	c.892G>A
AA Mutation	p.Glu298Lys(p.E298K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript