Primary Site >> Stomach Cancer
Gene >> GDF5
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000374369 |
| Start | 35434256:35434256(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs139413270 |
| CDS Mutation | c.1159C>T |
| AA Mutation | p.Arg387Cys(p.R387C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000374369 |
| Start | 35434418:35434418(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs767571173 |
| CDS Mutation | c.997G>A |
| AA Mutation | p.Ala333Thr(p.A333T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000374369 |
| Start | 35434217:35434217(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1198T>G |
| AA Mutation | p.Cys400Gly(p.C400G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000374369 |
| Start | 35437862:35437862(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.67T>C |
| AA Mutation | p.Cys23Arg(p.C23R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000374369 |
| Start | 35434568:35434568(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.847G>A |
| AA Mutation | p.Val283Met(p.V283M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000374369 |
| Start | 35434750:35434750(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.665A>G |
| AA Mutation | p.Tyr222Cys(p.Y222C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000374369 |
| Start | 35434513:35434513(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.902G>A |
| AA Mutation | p.Arg301Gln(p.R301Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000374369 |
| Start | 35437324:35437324(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.605T>C |
| AA Mutation | p.Ile202Thr(p.I202T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000374369 |
| Start | 35433978:35433978(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1437T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000374369 |
| Start | 35434242:35434242(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1173A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000374369 |
| Start | 35434083:35434083(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs529197082 |
| CDS Mutation | c.1332G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000374369 |
| Start | 35437431:35437431(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.498delC |
| AA Mutation | p.Ile167SerfsTer26(p.I167Sfs*26) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000374369 |
| Start | 35437632:35437632(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.297delC |
| AA Mutation | p.Arg100AspfsTer23(p.R100Dfs*23) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000374369 |
| Start | 35437724:35437724(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.205delG |
| AA Mutation | p.Ala69ProfsTer18(p.A69Pfs*18) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000374369 |
| Start | 35437631:35437632(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | rs761962752 |
| CDS Mutation | c.297dupC |
| AA Mutation | p.Arg100GlnfsTer6(p.R100Qfs*6) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000374369 |
| Start | 35437430:35437431(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.498dupC |
| AA Mutation | p.Ile167HisfsTer18(p.I167Hfs*18) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |