Primary Site >> Stomach Cancer
Gene >> LPA
| ID | 1 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000316300 |
| Start | 160585046:160585046(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs370793685 |
| CDS Mutation | c.4289C>T |
| AA Mutation | p.Ala1430Val(p.A1430V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000316300 |
| Start | 160589580:160589580(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3920A>G |
| AA Mutation | p.Gln1307Arg(p.Q1307R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000316300 |
| Start | 160650458:160650458(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.89A>G |
| AA Mutation | p.His30Arg(p.H30R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000316300 |
| Start | 160606531:160606531(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2731G>A |
| AA Mutation | p.Val911Ile(p.V911I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000316300 |
| Start | 160594085:160594085(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3502T>C |
| AA Mutation | p.Cys1168Arg(p.C1168R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000316300 |
| Start | 160611623:160611623(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2542C>A |
| AA Mutation | p.Gln848Lys(p.Q848K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000316300 |
| Start | 160650344:160650344(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.203C>T |
| AA Mutation | p.Pro68Leu(p.P68L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000316300 |
| Start | 160542705:160542705(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5502A>T |
| AA Mutation | p.Gln1834His(p.Q1834H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000316300 |
| Start | 160557431:160557431(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs768994342 |
| CDS Mutation | c.4772C>T |
| AA Mutation | p.Thr1591Ile(p.T1591I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000316300 |
| Start | 160532560:160532560(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5932C>T |
| AA Mutation | p.His1978Tyr(p.H1978Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000316300 |
| Start | 160593958:160593958(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3629G>A |
| AA Mutation | p.Gly1210Asp(p.G1210D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000316300 |
| Start | 160542705:160542705(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5502A>C |
| AA Mutation | p.Gln1834His(p.Q1834H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000316300 |
| Start | 160586532:160586532(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201200716 |
| CDS Mutation | c.4046C>T |
| AA Mutation | p.Thr1349Met(p.T1349M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000316300 |
| Start | 160599500:160599500(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs375355500 |
| CDS Mutation | c.3287C>T |
| AA Mutation | p.Ala1096Val(p.A1096V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000316300 |
| Start | 160633908:160633908(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs764520726 |
| CDS Mutation | c.1080G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000316300 |
| Start | 160601074:160601074(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2970A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000316300 |
| Start | 160586459:160586459(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4119T>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000316300 |
| Start | 160594098:160594098(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs758300066 |
| CDS Mutation | c.3489C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000316300 |
| Start | 160611681:160611681(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs569832683 |
| CDS Mutation | c.2484C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000316300 |
| Start | 160633872:160633872(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs373100474 |
| CDS Mutation | c.1116C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000316300 |
| Start | 160611588:160611588(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2577T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000316300 |
| Start | 160606535:160606535(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2727T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000316300 |
| Start | 160542738:160542738(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs757026230 |
| CDS Mutation | c.5469delG |
| AA Mutation | p.Cys1824ValfsTer27(p.C1824Vfs*27) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000316300 |
| Start | 160600924:160600924(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.3120delT |
| AA Mutation | p.Phe1040LeufsTer5(p.F1040Lfs*5) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 25 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000316300 |
| Start | 160611662:160611662(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs746733669 |
| CDS Mutation | c.2503C>T |
| AA Mutation | p.Arg835Ter(p.R835*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 26 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000316300 |
| Start | 160556150:160556150(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4848C>A |
| AA Mutation | p.Cys1616Ter(p.C1616*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 27 |
| Mutation Consequence | frameshift_variant;splice_region_variant |
| Transcription ID | ENST00000316300 |
| Start | 160547789:160547790(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | rs778676593 |
| CDS Mutation | c.5303dupA |
| AA Mutation | p.Asn1768LysfsTer5(p.N1768Kfs*5) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |
| ID | 28 |
| Mutation Consequence | splice_donor_variant |
| Transcription ID | ENST00000316300 |
| Start | 160611561:160611561(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs559580002 |
| CDS Mutation | c.2603+1G>A |
| Mutation Classification | Splice_Site |
| Feature Type | Transcript |