Primary Site >> Stomach Cancer
Gene >> DDR2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367921 |
| Start | 162754808:162754808(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.370C>T |
| AA Mutation | p.Arg124Trp(p.R124W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367921 |
| Start | 162778599:162778599(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2303G>C |
| AA Mutation | p.Ser768Thr(p.S768T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367921 |
| Start | 162753121:162753121(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.109T>G |
| AA Mutation | p.Ser37Ala(p.S37A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367921 |
| Start | 162780181:162780181(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2503G>T |
| AA Mutation | p.Asp835Tyr(p.D835Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367921 |
| Start | 162772143:162772143(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1624G>A |
| AA Mutation | p.Ala542Thr(p.A542T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367921 |
| Start | 162770440:162770440(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1432C>G |
| AA Mutation | p.Arg478Gly(p.R478G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367921 |
| Start | 162755210:162755210(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.472C>T |
| AA Mutation | p.Pro158Ser(p.P158S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367921 |
| Start | 162770360:162770360(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1352C>G |
| AA Mutation | p.Ser451Cys(p.S451C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367921 |
| Start | 162761377:162761377(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs769041297 |
| CDS Mutation | c.1022G>A |
| AA Mutation | p.Arg341Gln(p.R341Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367921 |
| Start | 162780194:162780194(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2516G>A |
| AA Mutation | p.Arg839His(p.R839H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000367921 |
| Start | 162770406:162770406(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1398G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000367921 |
| Start | 162775826:162775826(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs773962213 |
| CDS Mutation | c.2031C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000367921 |
| Start | 162755209:162755209(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs374094270 |
| CDS Mutation | c.471G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000367921 |
| Start | 162772049:162772049(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs751266189 |
| CDS Mutation | c.1530C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000367921 |
| Start | 162773571:162773571(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1831C>T |
| AA Mutation | p.Arg611Ter(p.R611*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |