Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> EIF3E

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000220849
Start	108217380:108217380(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.803G>A
AA Mutation	p.Arg268Gln(p.R268Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000220849
Start	108235027:108235027(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.442G>T
AA Mutation	p.Ala148Ser(p.A148S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000220849
Start	108203053:108203053(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1229G>A
AA Mutation	p.Ser410Asn(p.S410N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000220849
Start	108228320:108228320(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.669C>A
AA Mutation	p.Phe223Leu(p.F223L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000220849
Start	108203021:108203021(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1261A>C
AA Mutation	p.Asn421His(p.N421H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000220849
Start	108239990:108239990(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.291T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000220849
Start	108248662:108248662(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.41delT
AA Mutation	p.Leu14TrpfsTer5(p.L14Wfs*5)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	stop_gained
Transcription ID	ENST00000220849
Start	108217381:108217381(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.802C>T
AA Mutation	p.Arg268Ter(p.R268*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> EIF3E

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000220849
Start	108217380:108217380(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.803G>A
AA Mutation	p.Arg268Gln(p.R268Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript