Primary Site >> Stomach Cancer
Gene >> SF3A1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000215793 |
| Start | 30340803:30340803(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1081G>A |
| AA Mutation | p.Asp361Asn(p.D361N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000215793 |
| Start | 30335752:30335752(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2108G>A |
| AA Mutation | p.Gly703Asp(p.G703D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000215793 |
| Start | 30334641:30334641(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2335G>A |
| AA Mutation | p.Ala779Thr(p.A779T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000215793 |
| Start | 30342220:30342220(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.857A>G |
| AA Mutation | p.Asp286Gly(p.D286G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000215793 |
| Start | 30339213:30339213(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1414C>T |
| AA Mutation | p.Arg472Trp(p.R472W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000215793 |
| Start | 30338825:30338825(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs377308099 |
| CDS Mutation | c.1707G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000215793 |
| Start | 30334642:30334642(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs778333381 |
| CDS Mutation | c.2334C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000215793 |
| Start | 30338858:30338858(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs771207177 |
| CDS Mutation | c.1674G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |