Primary Site >> Stomach Cancer
Gene >> LPO
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262290 |
| Start | 58252204:58252204(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs773286393 |
| CDS Mutation | c.803C>T |
| AA Mutation | p.Ala268Val(p.A268V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262290 |
| Start | 58267492:58267492(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1837G>A |
| AA Mutation | p.Ala613Thr(p.A613T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262290 |
| Start | 58267518:58267518(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1863G>T |
| AA Mutation | p.Arg621Ser(p.R621S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262290 |
| Start | 58249153:58249153(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.419C>G |
| AA Mutation | p.Thr140Ser(p.T140S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262290 |
| Start | 58267991:58267991(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2136T>G |
| AA Mutation | p.Asn712Lys(p.N712K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262290 |
| Start | 58249588:58249588(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.466G>A |
| AA Mutation | p.Ala156Thr(p.A156T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262290 |
| Start | 58249585:58249585(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.463G>A |
| AA Mutation | p.Ala155Thr(p.A155T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262290 |
| Start | 58247558:58247558(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs765461792 |
| CDS Mutation | c.245G>A |
| AA Mutation | p.Arg82His(p.R82H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262290 |
| Start | 58249150:58249150(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.416G>A |
| AA Mutation | p.Arg139His(p.R139H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000262290 |
| Start | 58264832:58264832(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1377C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000262290 |
| Start | 58267458:58267458(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs141238819 |
| CDS Mutation | c.1803C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000262290 |
| Start | 58247585:58247585(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.274delG |
| AA Mutation | p.Glu92ArgfsTer4(p.E92Rfs*4) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |