Primary Site >> Stomach Cancer
Gene >> DMAP1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000315913 |
| Start | 44219192:44219192(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.857G>A |
| AA Mutation | p.Arg286His(p.R286H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000315913 |
| Start | 44220265:44220265(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1300G>A |
| AA Mutation | p.Asp434Asn(p.D434N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000315913 |
| Start | 44220230:44220230(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1265C>T |
| AA Mutation | p.Ala422Val(p.A422V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000315913 |
| Start | 44214782:44214782(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.277C>T |
| AA Mutation | p.Arg93Trp(p.R93W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000315913 |
| Start | 44220035:44220035(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1070C>T |
| AA Mutation | p.Thr357Met(p.T357M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000315913 |
| Start | 44219186:44219186(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.851C>T |
| AA Mutation | p.Thr284Met(p.T284M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000315913 |
| Start | 44219421:44219421(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.922G>A |
| AA Mutation | p.Ala308Thr(p.A308T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000315913 |
| Start | 44220196:44220196(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1231G>A |
| AA Mutation | p.Ala411Thr(p.A411T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000315913 |
| Start | 44214397:44214397(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.153G>T |
| AA Mutation | p.Glu51Asp(p.E51D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000315913 |
| Start | 44218414:44218414(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201828316 |
| CDS Mutation | c.497G>A |
| AA Mutation | p.Arg166His(p.R166H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000315913 |
| Start | 44214399:44214399(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.155G>A |
| AA Mutation | p.Gly52Asp(p.G52D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000315913 |
| Start | 44218334:44218334(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs145462822 |
| CDS Mutation | c.417G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000315913 |
| Start | 44220072:44220072(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs752229758 |
| CDS Mutation | c.1107C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |