Primary Site >> Stomach Cancer
Gene >> ERN1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000433197 |
| Start | 64045473:64045473(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs766760061 |
| CDS Mutation | c.2539G>A |
| AA Mutation | p.Asp847Asn(p.D847N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000433197 |
| Start | 64066745:64066745(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.768G>A |
| AA Mutation | p.Met256Ile(p.M256I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000433197 |
| Start | 64060563:64060563(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs376936066 |
| CDS Mutation | c.1112C>T |
| AA Mutation | p.Ala371Val(p.A371V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000433197 |
| Start | 64066839:64066839(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.674C>A |
| AA Mutation | p.Pro225His(p.P225H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000433197 |
| Start | 64047963:64047963(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2424G>C |
| AA Mutation | p.Leu808Phe(p.L808F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000433197 |
| Start | 64057986:64057986(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs780208953 |
| CDS Mutation | c.1214A>G |
| AA Mutation | p.Asn405Ser(p.N405S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000433197 |
| Start | 64054371:64054371(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1832G>A |
| AA Mutation | p.Arg611His(p.R611H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000433197 |
| Start | 64054378:64054378(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1825G>A |
| AA Mutation | p.Ala609Thr(p.A609T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000433197 |
| Start | 64072036:64072036(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs763718430 |
| CDS Mutation | c.423G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000433197 |
| Start | 64064086:64064086(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.987G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000433197 |
| Start | 64066847:64066847(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs757259673 |
| CDS Mutation | c.666C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000433197 |
| Start | 64072097:64072097(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.362delA |
| AA Mutation | p.Lys121SerfsTer11(p.K121Sfs*11) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000433197 |
| Start | 64045464:64045464(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2548G>T |
| AA Mutation | p.Glu850Ter(p.E850*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |