Primary Site >> Stomach Cancer
Gene >> MCM7
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000303887 |
| Start | 100097345:100097345(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1157C>A |
| AA Mutation | p.Ala386Asp(p.A386D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000303887 |
| Start | 100098643:100098643(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.655C>T |
| AA Mutation | p.Arg219Trp(p.R219W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000303887 |
| Start | 100094282:100094282(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1739A>G |
| AA Mutation | p.Tyr580Cys(p.Y580C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000303887 |
| Start | 100100054:100100054(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.71A>G |
| AA Mutation | p.Asp24Gly(p.D24G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000303887 |
| Start | 100095846:100095846(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1523C>T |
| AA Mutation | p.Pro508Leu(p.P508L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000303887 |
| Start | 100097737:100097737(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.994T>G |
| AA Mutation | p.Phe332Val(p.F332V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000303887 |
| Start | 100099345:100099345(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.335G>A |
| AA Mutation | p.Arg112Gln(p.R112Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000303887 |
| Start | 100097731:100097731(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs781082655 |
| CDS Mutation | c.1000G>A |
| AA Mutation | p.Glu334Lys(p.E334K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000303887 |
| Start | 100094314:100094314(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1707G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000303887 |
| Start | 100093004:100093004(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs139468339 |
| CDS Mutation | c.2088G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |