Mutation

Primary Site >> Stomach Cancer

Gene >> ARHGAP6

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000337414
Start	11144010:11144010(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2146G>A
AA Mutation	p.Glu716Lys(p.E716K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000337414
Start	11664255:11664255(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750456871
CDS Mutation	c.574G>A
AA Mutation	p.Val192Met(p.V192M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000337414
Start	11254619:11254619(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764970856
CDS Mutation	c.677G>A
AA Mutation	p.Arg226Gln(p.R226Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000337414
Start	11139065:11139065(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2723C>T
AA Mutation	p.Thr908Met(p.T908M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000337414
Start	11664380:11664380(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766331432
CDS Mutation	c.449G>A
AA Mutation	p.Arg150Gln(p.R150Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000337414
Start	11139338:11139338(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2450G>A
AA Mutation	p.Arg817His(p.R817H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000337414
Start	11169623:11169623(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1691A>G
AA Mutation	p.His564Arg(p.H564R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000337414
Start	11156591:11156591(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1845C>G
AA Mutation	p.Ser615Arg(p.S615R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000337414
Start	11664768:11664768(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.61G>A
AA Mutation	p.Ala21Thr(p.A21T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000337414
Start	11139109:11139109(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2679G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000337414
Start	11188854:11188854(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759569453
CDS Mutation	c.951A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000337414
Start	11144083:11144132(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2024_2073delTGCTGTCTGAGCGCTCCCTGCTGGCTATGCAAGAGGACGCGGCCCCGGGG
AA Mutation	p.Val675GlyfsTer69(p.V675Gfs*69)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	13
Mutation Consequence	stop_gained
Transcription ID	ENST00000337414
Start	11144021:11144021(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2135C>G
AA Mutation	p.Ser712Ter(p.S712*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000337414
Start	11664392:11664454(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.375_437delCCTGGGTCGCGGCGGCCTCAAGAAGAGCATGGCCTGGGACCTGCCTTCTGTCCTGGCCGGGCC
AA Mutation	p.Leu126_Pro146del(p.L126_P146del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript