Mutation

Primary Site >> Stomach Cancer

Gene >> EIF4B

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000262056
Start	53027839:53027839(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374172229
CDS Mutation	c.725G>A
AA Mutation	p.Arg242Gln(p.R242Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000262056
Start	53039325:53039325(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1664A>G
AA Mutation	p.His555Arg(p.H555R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000262056
Start	53018969:53018969(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.323C>T
AA Mutation	p.Thr108Ile(p.T108I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000262056
Start	53034652:53034652(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374072301
CDS Mutation	c.1249C>T
AA Mutation	p.Arg417Trp(p.R417W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000262056
Start	53018840:53018840(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764677800
CDS Mutation	c.194C>T
AA Mutation	p.Ala65Val(p.A65V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000262056
Start	53040191:53040191(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778266609
CDS Mutation	c.1804G>C
AA Mutation	p.Asp602His(p.D602H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000262056
Start	53028102:53028102(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.893A>G
AA Mutation	p.Tyr298Cys(p.Y298C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262056
Start	53019969:53019969(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.420T>C
Mutation Classification	Silent
Feature Type	Transcript