Primary Site >> Stomach Cancer
Gene >> MCM4
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262105 |
| Start | 47974893:47974893(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs149597772 |
| CDS Mutation | c.2296C>T |
| AA Mutation | p.Arg766Trp(p.R766W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262105 |
| Start | 47966283:47966283(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.929C>T |
| AA Mutation | p.Ala310Val(p.A310V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262105 |
| Start | 47975831:47975831(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs757711165 |
| CDS Mutation | c.2482C>T |
| AA Mutation | p.Arg828Trp(p.R828W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262105 |
| Start | 47974938:47974938(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs765226208 |
| CDS Mutation | c.2341G>A |
| AA Mutation | p.Val781Met(p.V781M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262105 |
| Start | 47973027:47973027(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2099C>T |
| AA Mutation | p.Pro700Leu(p.P700L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262105 |
| Start | 47976767:47976767(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs375720200 |
| CDS Mutation | c.2581C>T |
| AA Mutation | p.Arg861Cys(p.R861C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262105 |
| Start | 47975738:47975738(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs749728850 |
| CDS Mutation | c.2389C>T |
| AA Mutation | p.Arg797Trp(p.R797W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000262105 |
| Start | 47974960:47974960(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs781271560 |
| CDS Mutation | c.2363C>T |
| AA Mutation | p.Thr788Met(p.T788M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262105 |
| Start | 47976764:47976764(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs142208176 |
| CDS Mutation | c.2578G>A |
| AA Mutation | p.Val860Met(p.V860M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000262105 |
| Start | 47969895:47969895(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs376248536 |
| CDS Mutation | c.1272G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000262105 |
| Start | 47966338:47966338(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200670710 |
| CDS Mutation | c.984C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |