Primary Site >> Stomach Cancer
Gene >> MANEA
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000358812 |
| Start | 95605765:95605765(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.749C>T |
| AA Mutation | p.Ala250Val(p.A250V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000358812 |
| Start | 95586969:95586969(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs776967771 |
| CDS Mutation | c.530G>A |
| AA Mutation | p.Arg177His(p.R177H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000358812 |
| Start | 95586849:95586849(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.410A>G |
| AA Mutation | p.Lys137Arg(p.K137R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000358812 |
| Start | 95605762:95605762(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs770837820 |
| CDS Mutation | c.746C>T |
| AA Mutation | p.Pro249Leu(p.P249L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000358812 |
| Start | 95586608:95586608(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.169A>G |
| AA Mutation | p.Lys57Glu(p.K57E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000358812 |
| Start | 95606262:95606262(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1246C>T |
| AA Mutation | p.Pro416Ser(p.P416S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000358812 |
| Start | 95586956:95586956(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.517A>G |
| AA Mutation | p.Met173Val(p.M173V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000358812 |
| Start | 95586896:95586896(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.457A>T |
| AA Mutation | p.Ser153Cys(p.S153C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000358812 |
| Start | 95606236:95606236(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1220A>C |
| AA Mutation | p.Glu407Ala(p.E407A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000358812 |
| Start | 95586541:95586541(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.102T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000358812 |
| Start | 95605843:95605843(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.831delA |
| AA Mutation | p.Lys277AsnfsTer6(p.K277Nfs*6) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000358812 |
| Start | 95606142:95606142(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs765302262 |
| CDS Mutation | c.1126C>T |
| AA Mutation | p.Arg376Ter(p.R376*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000358812 |
| Start | 95604857:95604857(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs755535602 |
| CDS Mutation | c.685C>T |
| AA Mutation | p.Arg229Ter(p.R229*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |