Mutation

Primary Site >> Stomach Cancer

Gene >> PIK3CA

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000263967
Start	179219622:179219622(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1798G>A
AA Mutation	p.Glu600Lys(p.E600K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000263967
Start	179218303:179218303(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs104886003
CDS Mutation	c.1633G>A
AA Mutation	p.Glu545Lys(p.E545K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000263967
Start	179234297:179234297(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs121913279
CDS Mutation	c.3140A>G
AA Mutation	p.His1047Arg(p.H1047R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000263967
Start	179203765:179203765(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs121913284
CDS Mutation	c.1035T>A
AA Mutation	p.Asn345Lys(p.N345K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000263967
Start	179210192:179210192(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs121913272
CDS Mutation	c.1258T>C
AA Mutation	p.Cys420Arg(p.C420R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000263967
Start	179234219:179234219(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs121913288
CDS Mutation	c.3062A>G
AA Mutation	p.Tyr1021Cys(p.Y1021C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000263967
Start	179199148:179199148(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.323G>A
AA Mutation	p.Arg108His(p.R108H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000263967
Start	179234296:179234296(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs121913281
CDS Mutation	c.3139C>T
AA Mutation	p.His1047Tyr(p.H1047Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000263967
Start	179199088:179199088(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs121913287
CDS Mutation	c.263G>A
AA Mutation	p.Arg88Gln(p.R88Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000263967
Start	179204575:179204575(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1132T>C
AA Mutation	p.Cys378Arg(p.C378R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000263967
Start	179199690:179199690(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs587777790
CDS Mutation	c.353G>A
AA Mutation	p.Gly118Asp(p.G118D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000263967
Start	179199103:179199103(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.278G>A
AA Mutation	p.Arg93Gln(p.R93Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000263967
Start	179218308:179218308(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1638G>T
AA Mutation	p.Gln546His(p.Q546H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000263967
Start	179210291:179210291(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1357G>A
AA Mutation	p.Glu453Lys(p.E453K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000263967
Start	179218294:179218294(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs121913273
CDS Mutation	c.1624G>A
AA Mutation	p.Glu542Lys(p.E542K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000263967
Start	179199102:179199102(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.277C>T
AA Mutation	p.Arg93Trp(p.R93W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000263967
Start	179234218:179234218(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3061T>C
AA Mutation	p.Tyr1021His(p.Y1021H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000263967
Start	179198938:179198938(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772110575
CDS Mutation	c.113G>A
AA Mutation	p.Arg38His(p.R38H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000263967
Start	179199156:179199156(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.331A>G
AA Mutation	p.Lys111Glu(p.K111E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000263967
Start	179229412:179229412(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2636A>G
AA Mutation	p.Gln879Arg(p.Q879R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	21
Mutation Consequence	missense_variant
Transcription ID	ENST00000263967
Start	179203778:179203778(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1048G>A
AA Mutation	p.Asp350Asn(p.D350N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	22
Mutation Consequence	missense_variant
Transcription ID	ENST00000263967
Start	179218309:179218309(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1639G>A
AA Mutation	p.Glu547Lys(p.E547K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	23
Mutation Consequence	missense_variant
Transcription ID	ENST00000263967
Start	179198937:179198937(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749415085
CDS Mutation	c.112C>T
AA Mutation	p.Arg38Cys(p.R38C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	24
Mutation Consequence	missense_variant
Transcription ID	ENST00000263967
Start	179204536:179204536(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1093G>A
AA Mutation	p.Glu365Lys(p.E365K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	25
Mutation Consequence	missense_variant
Transcription ID	ENST00000263967
Start	179224123:179224123(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2230T>A
AA Mutation	p.Phe744Ile(p.F744I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	26
Mutation Consequence	missense_variant
Transcription ID	ENST00000263967
Start	179218304:179218304(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs121913274
CDS Mutation	c.1634A>G
AA Mutation	p.Glu545Gly(p.E545G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	27
Mutation Consequence	missense_variant
Transcription ID	ENST00000263967
Start	179209663:179209663(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1214C>T
AA Mutation	p.Ser405Phe(p.S405F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	28
Mutation Consequence	missense_variant
Transcription ID	ENST00000263967
Start	179199881:179199881(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.544T>C
AA Mutation	p.Tyr182His(p.Y182H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	29
Mutation Consequence	missense_variant
Transcription ID	ENST00000263967
Start	179218307:179218307(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs397517201
CDS Mutation	c.1637A>G
AA Mutation	p.Gln546Arg(p.Q546R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	30
Mutation Consequence	missense_variant
Transcription ID	ENST00000263967
Start	179234302:179234302(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs121913277
CDS Mutation	c.3145G>C
AA Mutation	p.Gly1049Arg(p.G1049R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	31
Mutation Consequence	missense_variant
Transcription ID	ENST00000263967
Start	179204582:179204582(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs202013300
CDS Mutation	c.1139A>G
AA Mutation	p.Asn380Ser(p.N380S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	32
Mutation Consequence	missense_variant
Transcription ID	ENST00000263967
Start	179204533:179204533(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1090G>A
AA Mutation	p.Gly364Arg(p.G364R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	33
Mutation Consequence	missense_variant
Transcription ID	ENST00000263967
Start	179230282:179230282(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2842A>G
AA Mutation	p.Lys948Glu(p.K948E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	34
Mutation Consequence	missense_variant
Transcription ID	ENST00000263967
Start	179234286:179234286(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs121913283
CDS Mutation	c.3129G>T
AA Mutation	p.Met1043Ile(p.M1043I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	35
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263967
Start	179219588:179219588(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1764A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	36
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263967
Start	179203705:179203705(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.975A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	37
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263967
Start	179199871:179199871(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.534A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	38
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263967
Start	179199143:179199143(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.318C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	39
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000263967
Start	179199886:179199887(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.552dupA
AA Mutation	p.Leu185IlefsTer3(p.L185Ifs*3)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	40
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000263967
Start	179234358:179234359(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.3203dupA
AA Mutation	p.Asn1068LysfsTer5(p.N1068Kfs*5)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	41
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000263967
Start	179199134:179199139(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.310_315delCCAGTA
AA Mutation	p.Pro104_Val105del(p.P104_V105del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript