Mutation

Primary Site >> Stomach Cancer

Gene >> PIK3C2A

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000265970
Start	17148733:17148733(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1382A>G
AA Mutation	p.Asp461Gly(p.D461G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000265970
Start	17117625:17117625(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752673250
CDS Mutation	c.3082G>A
AA Mutation	p.Glu1028Lys(p.E1028K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000265970
Start	17168804:17168804(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775520383
CDS Mutation	c.938C>T
AA Mutation	p.Ser313Leu(p.S313L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000265970
Start	17148773:17148773(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1342G>A
AA Mutation	p.Glu448Lys(p.E448K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000265970
Start	17112617:17112617(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3371T>C
AA Mutation	p.Val1124Ala(p.V1124A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000265970
Start	17119931:17119931(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2701T>C
AA Mutation	p.Tyr901His(p.Y901H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000265970
Start	17134965:17134965(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1962T>G
AA Mutation	p.Asp654Glu(p.D654E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000265970
Start	17117630:17117630(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3077G>A
AA Mutation	p.Arg1026Gln(p.R1026Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000265970
Start	17089778:17089778(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747006507
CDS Mutation	c.5021C>T
AA Mutation	p.Thr1674Met(p.T1674M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000265970
Start	17117661:17117661(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3046G>T
AA Mutation	p.Asp1016Tyr(p.D1016Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000265970
Start	17169218:17169218(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.524G>T
AA Mutation	p.Arg175Ile(p.R175I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000265970
Start	17091636:17091636(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4663A>G
AA Mutation	p.Thr1555Ala(p.T1555A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000265970
Start	17122236:17122236(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2609A>G
AA Mutation	p.Asp870Gly(p.D870G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265970
Start	17089780:17089780(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5019G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265970
Start	17094320:17094320(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749296923
CDS Mutation	c.4392C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265970
Start	17122322:17122322(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2523T>G
Mutation Classification	Silent
Feature Type	Transcript

ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265970
Start	17168893:17168893(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.849T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265970
Start	17135130:17135130(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1878T>A
Mutation Classification	Silent
Feature Type	Transcript

ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265970
Start	17129419:17129419(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2280T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	20
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000265970
Start	17169402:17169402(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.340delA
AA Mutation	p.Thr114HisfsTer10(p.T114Hfs*10)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	21
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000265970
Start	17169111:17169121(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.621_631delTCCACAAGGAA
AA Mutation	p.His207GlnfsTer12(p.H207Qfs*12)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	22
Mutation Consequence	stop_gained
Transcription ID	ENST00000265970
Start	17155539:17155539(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1156C>T
AA Mutation	p.Arg386Ter(p.R386*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	23
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000265970
Start	17091359:17091360(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.4852dupA
AA Mutation	p.Thr1618AsnfsTer8(p.T1618Nfs*8)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	24
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000265970
Start	17148665:17148665(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1448+2T>G
Mutation Classification	Splice_Site
Feature Type	Transcript