Primary Site >> Stomach Cancer
Gene >> SIPA1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394224 |
| Start | 65641112:65641112(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200828887 |
| CDS Mutation | c.191C>T |
| AA Mutation | p.Thr64Met(p.T64M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394224 |
| Start | 65644967:65644967(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs142497064 |
| CDS Mutation | c.997C>T |
| AA Mutation | p.Arg333Cys(p.R333C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394224 |
| Start | 65641129:65641129(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.208G>A |
| AA Mutation | p.Ala70Thr(p.A70T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394224 |
| Start | 65641453:65641453(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.532G>A |
| AA Mutation | p.Gly178Ser(p.G178S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394224 |
| Start | 65649610:65649610(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2575C>T |
| AA Mutation | p.Leu859Phe(p.L859F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394224 |
| Start | 65650409:65650409(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2912C>A |
| AA Mutation | p.Pro971His(p.P971H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394224 |
| Start | 65647506:65647506(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2154G>C |
| AA Mutation | p.Glu718Asp(p.E718D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394224 |
| Start | 65642373:65642373(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.803C>T |
| AA Mutation | p.Thr268Met(p.T268M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000394224 |
| Start | 65649648:65649648(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2613T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000394224 |
| Start | 65641146:65641146(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.225C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000394224 |
| Start | 65642525:65642525(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.870G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000394224 |
| Start | 65650464:65650464(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2967G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000394224 |
| Start | 65646361:65646361(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200729265 |
| CDS Mutation | c.1404G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000394224 |
| Start | 65642333:65642333(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.767delG |
| AA Mutation | p.Gly256AlafsTer48(p.G256Afs*48) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |