Primary Site >> Stomach Cancer
Gene >> MCM3
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000229854 |
| Start | 52282771:52282771(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.282G>C |
| AA Mutation | p.Gln94His(p.Q94H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000229854 |
| Start | 52267947:52267947(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs143308289 |
| CDS Mutation | c.1990C>T |
| AA Mutation | p.Arg664Cys(p.R664C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000229854 |
| Start | 52272306:52272306(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs754057696 |
| CDS Mutation | c.1822G>A |
| AA Mutation | p.Ala608Thr(p.A608T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000229854 |
| Start | 52269168:52269168(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs772883621 |
| CDS Mutation | c.1886C>T |
| AA Mutation | p.Ala629Val(p.A629V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000229854 |
| Start | 52282755:52282755(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs146219216 |
| CDS Mutation | c.298G>A |
| AA Mutation | p.Val100Ile(p.V100I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000229854 |
| Start | 52279487:52279487(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs377411679 |
| CDS Mutation | c.644G>A |
| AA Mutation | p.Arg215His(p.R215H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000229854 |
| Start | 52277614:52277614(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.954C>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |