Primary Site >> Stomach Cancer
Gene >> STAT5A
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000345506 |
| Start | 42301357:42301357(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1072G>A |
| AA Mutation | p.Gly358Arg(p.G358R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000345506 |
| Start | 42307699:42307699(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1882A>G |
| AA Mutation | p.Thr628Ala(p.T628A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000345506 |
| Start | 42289435:42289435(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.24G>T |
| AA Mutation | p.Gln8His(p.Q8H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000345506 |
| Start | 42304586:42304586(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1314G>T |
| AA Mutation | p.Glu438Asp(p.E438D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000345506 |
| Start | 42301377:42301377(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1092G>C |
| AA Mutation | p.Met364Ile(p.M364I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000345506 |
| Start | 42306318:42306318(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs369479819 |
| CDS Mutation | c.1551C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000345506 |
| Start | 42289477:42289477(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.66C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000345506 |
| Start | 42301381:42301381(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs759027671 |
| CDS Mutation | c.1102delC |
| AA Mutation | p.Gln368ArgfsTer2(p.Q368Rfs*2) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000345506 |
| Start | 42308251:42308251(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1984delG |
| AA Mutation | p.Asp662ThrfsTer2(p.D662Tfs*2) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000345506 |
| Start | 42295772:42295772(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.529C>T |
| AA Mutation | p.Gln177Ter(p.Q177*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |