Mutation

Primary Site >> Stomach Cancer

Gene >> PIK3CB

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000289153
Start	138707281:138707281(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1408G>A
AA Mutation	p.Glu470Lys(p.E470K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000289153
Start	138655451:138655451(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3151G>A
AA Mutation	p.Glu1051Lys(p.E1051K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000289153
Start	138734644:138734644(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.962G>A
AA Mutation	p.Arg321Gln(p.R321Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000289153
Start	138665133:138665133(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2575A>G
AA Mutation	p.Thr859Ala(p.T859A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000289153
Start	138691028:138691028(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2008A>T
AA Mutation	p.Ile670Leu(p.I670L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000289153
Start	138742707:138742707(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.472G>A
AA Mutation	p.Glu158Lys(p.E158K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000289153
Start	138714520:138714520(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143122477
CDS Mutation	c.1250C>T
AA Mutation	p.Thr417Met(p.T417M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000289153
Start	138698933:138698933(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1744T>C
AA Mutation	p.Trp582Arg(p.W582R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000289153
Start	138734706:138734706(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.900A>C
Mutation Classification	Silent
Feature Type	Transcript

ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000289153
Start	138657749:138657749(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2883C>G
Mutation Classification	Silent
Feature Type	Transcript

ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000289153
Start	138714687:138714687(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs377726824
CDS Mutation	c.1083T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000289153
Start	138742627:138742627(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.552C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000289153
Start	138712269:138712269(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1338delT
AA Mutation	p.Phe446LeufsTer7(p.F446Lfs*7)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000289153
Start	138714640:138714640(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1130delA
AA Mutation	p.Asn377MetfsTer35(p.N377Mfs*35)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	15
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000289153
Start	138663913:138663914(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.2788dupA
AA Mutation	p.Thr930AsnfsTer8(p.T930Nfs*8)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript