Mutation

Primary Site >> Stomach Cancer

Gene >> ARHGAP1

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000311956
Start	46680519:46680519(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.788T>C
AA Mutation	p.Leu263Pro(p.L263P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000311956
Start	46679728:46679728(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.947T>A
AA Mutation	p.Val316Asp(p.V316D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000311956
Start	46696054:46696054(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.54G>T
AA Mutation	p.Glu18Asp(p.E18D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000311956
Start	46688192:46688192(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs537320455
CDS Mutation	c.298G>A
AA Mutation	p.Asp100Asn(p.D100N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000311956
Start	46681368:46681368(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.461A>T
AA Mutation	p.Asn154Ile(p.N154I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000311956
Start	46696040:46696040(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.68T>C
AA Mutation	p.Leu23Pro(p.L23P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000311956
Start	46679707:46679707(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749420115
CDS Mutation	c.968G>A
AA Mutation	p.Arg323Gln(p.R323Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000311956
Start	46680738:46680738(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.645C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000311956
Start	46682125:46682125(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.375G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000311956
Start	46679169:46679169(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs528361008
CDS Mutation	c.1188C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000311956
Start	46679064:46679064(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1293C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000311956
Start	46680674:46680674(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.709delC
AA Mutation	p.Leu237CysfsTer135(p.L237Cfs*135)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	13
Mutation Consequence	inframe_insertion
Transcription ID	ENST00000311956
Start	46680697:46680698(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.685_686insTGTTGGCCAGGCTGATCTCAA
AA Mutation	p.Pro228_Lys229insMetLeuAlaArgLeuIleSer(p.P228_K229insMLARLIS)
Mutation Classification	In_Frame_Ins
Feature Type	Transcript