Primary Site >> Stomach Cancer
Gene >> RET
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000355710 |
| Start | 43114716:43114716(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs137855422 |
| CDS Mutation | c.2116G>A |
| AA Mutation | p.Val706Met(p.V706M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000355710 |
| Start | 43111295:43111295(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs774092678 |
| CDS Mutation | c.1352C>T |
| AA Mutation | p.Thr451Met(p.T451M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000355710 |
| Start | 43118465:43118465(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2377G>A |
| AA Mutation | p.Ala793Thr(p.A793T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000355710 |
| Start | 43106463:43106463(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.955C>T |
| AA Mutation | p.Leu319Phe(p.L319F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000355710 |
| Start | 43113634:43113634(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs761596036 |
| CDS Mutation | c.1838C>T |
| AA Mutation | p.Pro613Leu(p.P613L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000355710 |
| Start | 43111286:43111286(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1343A>G |
| AA Mutation | p.Asn448Ser(p.N448S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000355710 |
| Start | 43100591:43100591(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.206G>A |
| AA Mutation | p.Gly69Asp(p.G69D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000355710 |
| Start | 43120193:43120193(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2720A>C |
| AA Mutation | p.Lys907Thr(p.K907T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000355710 |
| Start | 43102617:43102617(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.613A>G |
| AA Mutation | p.Arg205Gly(p.R205G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000355710 |
| Start | 43124968:43124968(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3025A>G |
| AA Mutation | p.Met1009Val(p.M1009V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000355710 |
| Start | 43116609:43116609(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2162G>A |
| AA Mutation | p.Arg721Gln(p.R721Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000355710 |
| Start | 43126669:43126669(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3134A>G |
| AA Mutation | p.Asn1045Ser(p.N1045S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000355710 |
| Start | 43106554:43106554(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs754859905 |
| CDS Mutation | c.1046C>T |
| AA Mutation | p.Ala349Val(p.A349V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000355710 |
| Start | 43106445:43106445(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.937C>T |
| AA Mutation | p.Arg313Trp(p.R313W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000355710 |
| Start | 43126671:43126671(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3136G>A |
| AA Mutation | p.Ala1046Thr(p.A1046T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000355710 |
| Start | 43121978:43121978(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2763A>T |
| AA Mutation | p.Glu921Asp(p.E921D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000355710 |
| Start | 43105017:43105017(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.691C>T |
| AA Mutation | p.Arg231Cys(p.R231C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000355710 |
| Start | 43111238:43111238(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs552057730 |
| CDS Mutation | c.1295C>T |
| AA Mutation | p.Ala432Val(p.A432V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000355710 |
| Start | 43112902:43112902(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs760507059 |
| CDS Mutation | c.1698C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000355710 |
| Start | 43105160:43105160(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs41306550 |
| CDS Mutation | c.834C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000355710 |
| Start | 43105169:43105169(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs770794801 |
| CDS Mutation | c.843C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000355710 |
| Start | 43119685:43119685(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs770674650 |
| CDS Mutation | c.2547C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000355710 |
| Start | 43126625:43126625(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs142859395 |
| CDS Mutation | c.3090C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000355710 |
| Start | 43123716:43123716(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.2849delA |
| AA Mutation | p.Asn950ThrfsTer15(p.N950Tfs*15) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |