Mutation

Primary Site >> Stomach Cancer

Gene >> G3BP1

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000356245
Start	151799892:151799892(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.847C>T
AA Mutation	p.Arg283Cys(p.R283C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000356245
Start	151790976:151790976(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.265G>T
AA Mutation	p.Gly89Cys(p.G89C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000356245
Start	151800296:151800296(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1034G>A
AA Mutation	p.Gly345Asp(p.G345D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000356245
Start	151803909:151803909(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1219C>T
AA Mutation	p.Arg407Cys(p.R407C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000356245
Start	151799914:151799914(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.869C>G
AA Mutation	p.Ser290Cys(p.S290C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000356245
Start	151791049:151791049(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.338T>C
AA Mutation	p.Val113Ala(p.V113A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000356245
Start	151786628:151786628(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769813798
CDS Mutation	c.8T>C
AA Mutation	p.Met3Thr(p.M3T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356245
Start	151799975:151799975(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.930T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000356245
Start	151799295:151799296(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.828dupA
AA Mutation	p.Val277SerfsTer11(p.V277Sfs*11)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript