Mutation

Primary Site >> Stomach Cancer

Gene >> ITGA2B

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000262407
Start	44384556:44384556(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.829G>A
AA Mutation	p.Gly277Arg(p.G277R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000262407
Start	44379747:44379747(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs539187844
CDS Mutation	c.1820C>T
AA Mutation	p.Thr607Met(p.T607M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000262407
Start	44380024:44380024(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1730A>G
AA Mutation	p.His577Arg(p.H577R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000262407
Start	44374709:44374709(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2893T>C
AA Mutation	p.Ser965Pro(p.S965P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000262407
Start	44385892:44385892(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.340A>C
AA Mutation	p.Thr114Pro(p.T114P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000262407
Start	44380600:44380600(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1439G>T
AA Mutation	p.Arg480Ile(p.R480I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000262407
Start	44385178:44385178(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.656G>A
AA Mutation	p.Gly219Asp(p.G219D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000262407
Start	44376089:44376089(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2444A>G
AA Mutation	p.Tyr815Cys(p.Y815C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000262407
Start	44383657:44383657(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1046C>T
AA Mutation	p.Ala349Val(p.A349V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000262407
Start	44379702:44379702(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1865A>G
AA Mutation	p.His622Arg(p.H622R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000262407
Start	44379798:44379798(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747930676
CDS Mutation	c.1769G>A
AA Mutation	p.Arg590Gln(p.R590Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262407
Start	44375594:44375594(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2724C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262407
Start	44389366:44389366(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.108A>T
Mutation Classification	Silent
Feature Type	Transcript

ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262407
Start	44380092:44380092(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1662G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262407
Start	44389342:44389342(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.132C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	16
Mutation Consequence	stop_gained
Transcription ID	ENST00000262407
Start	44383640:44383640(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1063G>T
AA Mutation	p.Glu355Ter(p.E355*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	stop_gained
Transcription ID	ENST00000262407
Start	44385910:44385910(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.322C>T
AA Mutation	p.Arg108Ter(p.R108*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript