Primary Site >> Stomach Cancer
Gene >> STIM1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000300737 |
| Start | 4023877:4023877(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.275T>C |
| AA Mutation | p.Leu92Pro(p.L92P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000300737 |
| Start | 4083294:4083294(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1270C>T |
| AA Mutation | p.Arg424Trp(p.R424W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000300737 |
| Start | 4074606:4074606(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.896G>T |
| AA Mutation | p.Arg299Leu(p.R299L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000300737 |
| Start | 3856283:3856283(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs150529970 |
| CDS Mutation | c.13G>A |
| AA Mutation | p.Val5Ile(p.V5I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000300737 |
| Start | 4091668:4091668(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs140080199 |
| CDS Mutation | c.1928G>A |
| AA Mutation | p.Arg643His(p.R643H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000300737 |
| Start | 4091298:4091298(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs199914458 |
| CDS Mutation | c.1558G>A |
| AA Mutation | p.Asp520Asn(p.D520N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000300737 |
| Start | 4091404:4091404(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200525396 |
| CDS Mutation | c.1664G>A |
| AA Mutation | p.Gly555Asp(p.G555D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000300737 |
| Start | 4091749:4091749(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2009G>A |
| AA Mutation | p.Gly670Asp(p.G670D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000300737 |
| Start | 4091303:4091303(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs148209416 |
| CDS Mutation | c.1563G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000300737 |
| Start | 4059357:4059357(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.574C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000300737 |
| Start | 4091702:4091702(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1962T>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000300737 |
| Start | 4082956:4082956(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs763198159 |
| CDS Mutation | c.1212T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |