Mutation

Primary Site >> Stomach Cancer

Gene >> ARHGAP5

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000345122
Start	32092062:32092062(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1393T>C
AA Mutation	p.Tyr465His(p.Y465H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000345122
Start	32090694:32090694(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781445770
CDS Mutation	c.25C>T
AA Mutation	p.Arg9Cys(p.R9C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000345122
Start	32091262:32091262(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.593C>G
AA Mutation	p.Ala198Gly(p.A198G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000345122
Start	32092623:32092623(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs146396734
CDS Mutation	c.1954G>A
AA Mutation	p.Ala652Thr(p.A652T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000345122
Start	32093481:32093481(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2812G>T
AA Mutation	p.Val938Phe(p.V938F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000345122
Start	32091715:32091715(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1046T>C
AA Mutation	p.Leu349Pro(p.L349P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000345122
Start	32091021:32091021(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.352C>T
AA Mutation	p.Arg118Cys(p.R118C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000345122
Start	32094159:32094159(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3490G>A
AA Mutation	p.Ala1164Thr(p.A1164T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000345122
Start	32092112:32092112(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1443A>C
AA Mutation	p.Glu481Asp(p.E481D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000345122
Start	32092009:32092009(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1340G>A
AA Mutation	p.Gly447Glu(p.G447E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000345122
Start	32092075:32092075(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1406C>T
AA Mutation	p.Ala469Val(p.A469V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000345122
Start	32093018:32093018(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs61737878
CDS Mutation	c.2349C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000345122
Start	32154714:32154714(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4275A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000345122
Start	32093633:32093633(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs567946684
CDS Mutation	c.2964A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000345122
Start	32092622:32092622(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757953107
CDS Mutation	c.1953C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	16
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000345122
Start	32093490:32093490(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2828delA
AA Mutation	p.Asn943IlefsTer2(p.N943Ifs*2)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	17
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000345122
Start	32091692:32091705(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1025_1038delTACCAAGAGCTTTT
AA Mutation	p.Leu342Ter(p.L342*)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	18
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000345122
Start	32093140:32093140(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2476delA
AA Mutation	p.Arg826GlyfsTer17(p.R826Gfs*17)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	19
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000345122
Start	32093339:32093339(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs781483073
CDS Mutation	c.2676delT
AA Mutation	p.Phe892LeufsTer9(p.F892Lfs*9)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	20
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000345122
Start	32093469:32093469(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2805delT
AA Mutation	p.Phe935LeufsTer5(p.F935Lfs*5)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	21
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000345122
Start	32091939:32091943(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1273_1277delAAGAG
AA Mutation	p.Lys425GlufsTer35(p.K425Efs*35)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	22
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000345122
Start	32092120:32092120(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1455delA
AA Mutation	p.Ala486ProfsTer19(p.A486Pfs*19)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	23
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000345122
Start	32091239:32091239(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.576delA
AA Mutation	p.Lys192AsnfsTer3(p.K192Nfs*3)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	24
Mutation Consequence	stop_gained
Transcription ID	ENST00000345122
Start	32092308:32092308(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1639G>T
AA Mutation	p.Gly547Ter(p.G547*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	25
Mutation Consequence	stop_gained
Transcription ID	ENST00000345122
Start	32092616:32092616(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1947G>A
AA Mutation	p.Trp649Ter(p.W649*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	26
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000345122
Start	32093338:32093339(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.2676dupT
AA Mutation	p.Glu893Ter(p.E893*)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	27
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000345122
Start	32093139:32093140(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.2476dupA
AA Mutation	p.Arg826LysfsTer21(p.R826Kfs*21)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	28
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000345122
Start	32091238:32091239(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.576dupA
AA Mutation	p.Pro193ThrfsTer8(p.P193Tfs*8)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript