Mutation

Primary Site >> Stomach Cancer

Gene >> EIF3A

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000369144
Start	119065566:119065566(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.955T>C
AA Mutation	p.Ser319Pro(p.S319P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000369144
Start	119050633:119050633(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2361G>C
AA Mutation	p.Arg787Ser(p.R787S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000369144
Start	119059268:119059268(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1573G>T
AA Mutation	p.Ala525Ser(p.A525S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000369144
Start	119050589:119050589(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2405G>A
AA Mutation	p.Arg802His(p.R802H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000369144
Start	119042714:119042714(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762013834
CDS Mutation	c.2806C>T
AA Mutation	p.Arg936Trp(p.R936W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000369144
Start	119065514:119065514(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755084308
CDS Mutation	c.1007C>T
AA Mutation	p.Thr336Met(p.T336M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000369144
Start	119050601:119050601(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2393G>A
AA Mutation	p.Arg798His(p.R798H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000369144
Start	119036091:119036091(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143903271
CDS Mutation	c.4097G>A
AA Mutation	p.Arg1366His(p.R1366H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000369144
Start	119038253:119038253(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3713G>A
AA Mutation	p.Arg1238His(p.R1238H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369144
Start	119042661:119042661(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148664870
CDS Mutation	c.2859C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369144
Start	119059347:119059347(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1494T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369144
Start	119050603:119050603(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2391G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000369144
Start	119049903:119049903(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2556delA
AA Mutation	p.Glu853LysfsTer320(p.E853Kfs*320)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	14
Mutation Consequence	stop_gained
Transcription ID	ENST00000369144
Start	119037179:119037179(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3859C>T
AA Mutation	p.Arg1287Ter(p.R1287*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript