Primary Site >> Stomach Cancer
Gene >> TOP1MT
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000329245 |
| Start | 143315805:143315805(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1475A>G |
| AA Mutation | p.Glu492Gly(p.E492G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000329245 |
| Start | 143309467:143309467(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1780A>G |
| AA Mutation | p.Met594Val(p.M594V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000329245 |
| Start | 143315769:143315769(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1511C>T |
| AA Mutation | p.Ala504Val(p.A504V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000329245 |
| Start | 143324049:143324049(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.910C>T |
| AA Mutation | p.Arg304Trp(p.R304W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000329245 |
| Start | 143321344:143321344(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1003G>A |
| AA Mutation | p.Ala335Thr(p.A335T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000329245 |
| Start | 143324561:143324561(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs150737353 |
| CDS Mutation | c.740C>T |
| AA Mutation | p.Thr247Met(p.T247M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000329245 |
| Start | 143310176:143310176(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1595A>C |
| AA Mutation | p.Glu532Ala(p.E532A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000329245 |
| Start | 143325419:143325419(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs146761712 |
| CDS Mutation | c.598C>T |
| AA Mutation | p.Arg200Cys(p.R200C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000329245 |
| Start | 143325518:143325518(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.499G>A |
| AA Mutation | p.Ala167Thr(p.A167T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000329245 |
| Start | 143315787:143315787(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1493G>T |
| AA Mutation | p.Arg498Met(p.R498M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000329245 |
| Start | 143324505:143324505(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.796A>G |
| AA Mutation | p.Asn266Asp(p.N266D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000329245 |
| Start | 143309482:143309482(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs374238650 |
| CDS Mutation | c.1765G>A |
| AA Mutation | p.Ala589Thr(p.A589T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000329245 |
| Start | 143321306:143321306(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1041C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000329245 |
| Start | 143324575:143324575(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs377344559 |
| CDS Mutation | c.726C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000329245 |
| Start | 143317766:143317766(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs143974988 |
| CDS Mutation | c.1287C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000329245 |
| Start | 143331273:143331273(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs756698265 |
| CDS Mutation | c.189C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |