Primary Site >> Stomach Cancer
Gene >> RB1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000267163 |
| Start | 48465242:48465242(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2363G>A |
| AA Mutation | p.Ser788Asn(p.S788N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000267163 |
| Start | 48368570:48368570(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1093G>C |
| AA Mutation | p.Glu365Gln(p.E365Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000267163 |
| Start | 48345099:48345099(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.400T>G |
| AA Mutation | p.Leu134Val(p.L134V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000267163 |
| Start | 48373412:48373412(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1135A>T |
| AA Mutation | p.Met379Leu(p.M379L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000267163 |
| Start | 48465225:48465225(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2346A>G |
| AA Mutation | p.Ile782Met(p.I782M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000267163 |
| Start | 48380191:48380191(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1448A>G |
| AA Mutation | p.His483Arg(p.H483R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000267163 |
| Start | 48377033:48377033(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1331A>T |
| AA Mutation | p.Gln444Leu(p.Q444L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000267163 |
| Start | 48345169:48345169(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.470T>C |
| AA Mutation | p.Val157Ala(p.V157A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000267163 |
| Start | 48456249:48456249(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs750356534 |
| CDS Mutation | c.1860G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000267163 |
| Start | 48345182:48345182(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.483C>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000267163 |
| Start | 48456232:48456232(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1848delA |
| AA Mutation | p.Gly617ValfsTer6(p.G617Vfs*6) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000267163 |
| Start | 48362907:48362910(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.811_814delACAA |
| AA Mutation | p.Thr271GlufsTer14(p.T271Efs*14) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000267163 |
| Start | 48362847:48362847(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.751C>T |
| AA Mutation | p.Arg251Ter(p.R251*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000267163 |
| Start | 48381402:48381402(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs121913303 |
| CDS Mutation | c.1654C>T |
| AA Mutation | p.Arg552Ter(p.R552*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000267163 |
| Start | 48367512:48367512(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs121913300 |
| CDS Mutation | c.958C>T |
| AA Mutation | p.Arg320Ter(p.R320*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | inframe_deletion |
| Transcription ID | ENST00000267163 |
| Start | 48459771:48459785(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.2049_2063delTTTCCAGCACACCCT |
| AA Mutation | p.Phe684_Leu688del(p.F684_L688del) |
| Mutation Classification | In_Frame_Del |
| Feature Type | Transcript |