Mutation

Primary Site >> Stomach Cancer

Gene >> PTEN

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000371953
Start	87952125:87952125(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.500C>G
AA Mutation	p.Thr167Ser(p.T167S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000371953
Start	87933130:87933130(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.371G>C
AA Mutation	p.Cys124Ser(p.C124S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000371953
Start	87933236:87933236(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.477G>T
AA Mutation	p.Arg159Ser(p.R159S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000371953
Start	87894028:87894028(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.83T>G
AA Mutation	p.Ile28Ser(p.I28S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000371953
Start	87864541:87864541(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.72C>G
AA Mutation	p.Asp24Glu(p.D24E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000371953
Start	87933148:87933148(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs121909229
CDS Mutation	c.389G>A
AA Mutation	p.Arg130Gln(p.R130Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000371953
Start	87933136:87933136(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.377C>A
AA Mutation	p.Ala126Asp(p.A126D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371953
Start	87925546:87925546(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.198G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371953
Start	87894044:87894044(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs786201650
CDS Mutation	c.99T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371953
Start	87957956:87957956(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774364894
CDS Mutation	c.738G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000371953
Start	87965295:87965310(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1038_1053delCTTCACAAAAACAGTA
AA Mutation	p.Tyr346Ter(p.Y346*)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000371953
Start	87958013:87958013(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.800delA
AA Mutation	p.Lys267ArgfsTer9(p.K267Rfs*9)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000371953
Start	87961055:87961055(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.968delA
AA Mutation	p.Asn323MetfsTer21(p.N323Mfs*21)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000371953
Start	87933246:87933246(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.491delA
AA Mutation	p.Lys164ArgfsTer3(p.K164Rfs*3)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	15
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000371953
Start	87864533:87864543(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.67_77delTTAGACTTGAC
AA Mutation	p.Asp24TyrfsTer16(p.D24Yfs*16)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	16
Mutation Consequence	stop_gained
Transcription ID	ENST00000371953
Start	87957915:87957915(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs121909219
CDS Mutation	c.697C>T
AA Mutation	p.Arg233Ter(p.R233*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000371953
Start	87961022:87961023(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.930_931insC
AA Mutation	p.Asn311GlnfsTer2(p.N311Qfs*2)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	18
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000371953
Start	87961054:87961055(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.968dupA
AA Mutation	p.Asn323LysfsTer2(p.N323Kfs*2)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	19
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000371953
Start	87957908:87957909(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.693dupC
AA Mutation	p.Thr232HisfsTer11(p.T232Hfs*11)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	20
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000371953
Start	87894111:87894111(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.164+2T>C
Mutation Classification	Splice_Site
Feature Type	Transcript

ID	21
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000371953
Start	87961029:87961115(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.941_1026+1delAATATCTAGTACTTACTTTAACAAAAAATGATCTTGACAAAGCAAATAAAGACAAAGCCAACCGATACTTTTCTCCAAATTTTAAGG
Mutation Classification	In_Frame_Del
Feature Type	Transcript