Mutation

Primary Site >> Stomach Cancer

Gene >> PIK3CG

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000359195
Start	106867812:106867812(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766854286
CDS Mutation	c.251C>T
AA Mutation	p.Ala84Val(p.A84V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000359195
Start	106868640:106868640(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1079A>G
AA Mutation	p.Lys360Arg(p.K360R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000359195
Start	106868126:106868126(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.565G>A
AA Mutation	p.Ala189Thr(p.A189T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000359195
Start	106867830:106867830(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749392283
CDS Mutation	c.269G>A
AA Mutation	p.Arg90Gln(p.R90Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000359195
Start	106868228:106868228(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs554272230
CDS Mutation	c.667G>A
AA Mutation	p.Val223Ile(p.V223I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000359195
Start	106868288:106868288(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.727G>A
AA Mutation	p.Ala243Thr(p.A243T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000359195
Start	106883147:106883147(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2744C>T
AA Mutation	p.Ser915Phe(p.S915F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000359195
Start	106868633:106868633(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs62001903
CDS Mutation	c.1072G>A
AA Mutation	p.Asp358Asn(p.D358N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000359195
Start	106867928:106867928(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.367C>T
AA Mutation	p.Arg123Cys(p.R123C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000359195
Start	106879555:106879555(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759433704
CDS Mutation	c.2428C>A
AA Mutation	p.Pro810Thr(p.P810T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000359195
Start	106867620:106867620(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.59G>A
AA Mutation	p.Arg20His(p.R20H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000359195
Start	106869396:106869396(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1835C>T
AA Mutation	p.Ala612Val(p.A612V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000359195
Start	106867614:106867614(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs142380460
CDS Mutation	c.53G>A
AA Mutation	p.Arg18Gln(p.R18Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000359195
Start	106867949:106867949(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.388C>T
AA Mutation	p.Arg130Trp(p.R130W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000359195
Start	106868919:106868919(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1358A>G
AA Mutation	p.Glu453Gly(p.E453G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000359195
Start	106868136:106868136(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.575A>G
AA Mutation	p.Asp192Gly(p.D192G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000359195
Start	106868045:106868045(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.484G>A
AA Mutation	p.Val162Ile(p.V162I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000359195
Start	106868348:106868348(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370152741
CDS Mutation	c.787G>A
AA Mutation	p.Glu263Lys(p.E263K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000359195
Start	106882161:106882161(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2583T>A
AA Mutation	p.Asp861Glu(p.D861E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000359195
Start	106905127:106905127(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3049T>C
AA Mutation	p.Tyr1017His(p.Y1017H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	21
Mutation Consequence	missense_variant
Transcription ID	ENST00000359195
Start	106868016:106868016(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762164881
CDS Mutation	c.455G>A
AA Mutation	p.Arg152Gln(p.R152Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359195
Start	106869166:106869166(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1605C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359195
Start	106879632:106879632(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2505T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359195
Start	106905153:106905153(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3075C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359195
Start	106869001:106869001(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756992475
CDS Mutation	c.1440C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	26
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359195
Start	106869301:106869301(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201753163
CDS Mutation	c.1740C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	27
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359195
Start	106868380:106868380(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766076868
CDS Mutation	c.819C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	28
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359195
Start	106868068:106868068(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.507C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	29
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359195
Start	106872875:106872875(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2224T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	30
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000359195
Start	106879549:106879549(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2427delA
AA Mutation	p.Lys809AsnfsTer68(p.K809Nfs*68)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	31
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000359195
Start	106868550:106868550(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.989delC
AA Mutation	p.Thr330ArgfsTer54(p.T330Rfs*54)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	32
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000359195
Start	106872939:106872939(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2287+1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript