Mutation

Primary Site >> Stomach Cancer

Gene >> ARHGAP35

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000404338
Start	46918805:46918805(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774121374
CDS Mutation	c.130C>T
AA Mutation	p.Arg44Cys(p.R44C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000404338
Start	46922097:46922097(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3422G>A
AA Mutation	p.Ser1141Asn(p.S1141N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000404338
Start	46989588:46989588(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3949G>A
AA Mutation	p.Val1317Met(p.V1317M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000404338
Start	46918806:46918806(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759238695
CDS Mutation	c.131G>A
AA Mutation	p.Arg44His(p.R44H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000404338
Start	46919654:46919654(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199897795
CDS Mutation	c.979C>T
AA Mutation	p.Arg327Cys(p.R327C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000404338
Start	46918802:46918802(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.127G>A
AA Mutation	p.Val43Met(p.V43M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000404338
Start	46921827:46921827(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3152T>A
AA Mutation	p.Ile1051Asn(p.I1051N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000404338
Start	46921290:46921290(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2615C>T
AA Mutation	p.Ala872Val(p.A872V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000404338
Start	46919816:46919816(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1141G>T
AA Mutation	p.Val381Phe(p.V381F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000404338
Start	47000503:47000503(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4315C>T
AA Mutation	p.Arg1439Trp(p.R1439W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000404338
Start	46920902:46920902(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2227G>A
AA Mutation	p.Gly743Arg(p.G743R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000404338
Start	47000674:47000674(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4486G>A
AA Mutation	p.Glu1496Lys(p.E1496K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000404338
Start	46921136:46921136(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2461T>G
AA Mutation	p.Leu821Val(p.L821V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000404338
Start	46921500:46921500(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2825T>C
AA Mutation	p.Val942Ala(p.V942A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000404338
Start	46922115:46922115(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3440G>A
AA Mutation	p.Arg1147His(p.R1147H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000404338
Start	46918732:46918732(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.57G>T
Mutation Classification	Silent
Feature Type	Transcript

ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000404338
Start	46918810:46918810(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767399152
CDS Mutation	c.135G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000404338
Start	46918801:46918801(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772729752
CDS Mutation	c.126C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000404338
Start	46920367:46920367(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1692T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000404338
Start	46920685:46920685(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2010G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	21
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000404338
Start	46919333:46919333(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.662delA
AA Mutation	p.Lys221ArgfsTer14(p.K221Rfs*14)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	22
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000404338
Start	46921503:46921503(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2834delA
AA Mutation	p.Lys945ArgfsTer3(p.K945Rfs*3)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	23
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000404338
Start	46921584:46921584(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2914delC
AA Mutation	p.Arg972GlyfsTer55(p.R972Gfs*55)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	24
Mutation Consequence	stop_gained
Transcription ID	ENST00000404338
Start	46921664:46921664(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2989C>T
AA Mutation	p.Arg997Ter(p.R997*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	25
Mutation Consequence	stop_gained
Transcription ID	ENST00000404338
Start	46922108:46922108(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3433C>T
AA Mutation	p.Arg1145Ter(p.R1145*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	26
Mutation Consequence	stop_gained
Transcription ID	ENST00000404338
Start	46919972:46919972(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1297C>T
AA Mutation	p.Arg433Ter(p.R433*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	27
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000404338
Start	46920591:46920592(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1918dupA
AA Mutation	p.Ile640AsnfsTer43(p.I640Nfs*43)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript