Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> EIF5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000216554
Start	103339786:103339786(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1054A>G
AA Mutation	p.Ile352Val(p.I352V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000216554
Start	103336809:103336809(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.287T>G
AA Mutation	p.Phe96Cys(p.F96C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000216554
Start	103340519:103340519(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1164A>C
AA Mutation	p.Glu388Asp(p.E388D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	stop_gained
Transcription ID	ENST00000216554
Start	103336793:103336793(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.271G>T
AA Mutation	p.Gly91Ter(p.G91*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> EIF5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000216554
Start	103335885:103335885(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768072672
CDS Mutation	c.25G>A
AA Mutation	p.Val9Met(p.V9M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000216554
Start	103336686:103336686(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.164A>C
AA Mutation	p.Lys55Thr(p.K55T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000216554
Start	103340992:103340992(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140137312
CDS Mutation	c.1236G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	stop_gained
Transcription ID	ENST00000216554
Start	103338356:103338356(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.469G>T
AA Mutation	p.Glu157Ter(p.E157*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript