Primary Site >> Stomach Cancer
Gene >> PLOD3
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000223127 |
| Start | 101210405:101210405(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs746896780 |
| CDS Mutation | c.1540C>T |
| AA Mutation | p.Arg514Trp(p.R514W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000223127 |
| Start | 101210669:101210669(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1363G>A |
| AA Mutation | p.Val455Met(p.V455M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000223127 |
| Start | 101206312:101206312(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2186G>A |
| AA Mutation | p.Arg729His(p.R729H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000223127 |
| Start | 101206340:101206340(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2158G>A |
| AA Mutation | p.Glu720Lys(p.E720K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000223127 |
| Start | 101212326:101212326(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1054G>T |
| AA Mutation | p.Asp352Tyr(p.D352Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000223127 |
| Start | 101216189:101216189(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs763102265 |
| CDS Mutation | c.476C>T |
| AA Mutation | p.Thr159Met(p.T159M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000223127 |
| Start | 101210615:101210615(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs770056635 |
| CDS Mutation | c.1417C>T |
| AA Mutation | p.Arg473Trp(p.R473W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000223127 |
| Start | 101216501:101216501(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.247A>G |
| AA Mutation | p.Thr83Ala(p.T83A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000223127 |
| Start | 101216242:101216242(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.423G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000223127 |
| Start | 101212273:101212273(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs193247871 |
| CDS Mutation | c.1107C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000223127 |
| Start | 101216188:101216188(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201433094 |
| CDS Mutation | c.477G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000223127 |
| Start | 101211929:101211929(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs767540894 |
| CDS Mutation | c.1149C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000223127 |
| Start | 101212646:101212646(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs780620804 |
| CDS Mutation | c.889delC |
| AA Mutation | p.Arg297GlyfsTer61(p.R297Gfs*61) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000223127 |
| Start | 101212845:101212845(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.876delG |
| AA Mutation | p.Gln293SerfsTer65(p.Q293Sfs*65) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000223127 |
| Start | 101215974:101215974(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.549G>A |
| AA Mutation | p.Trp183Ter(p.W183*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000223127 |
| Start | 101212645:101212646(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | rs770446713 |
| CDS Mutation | c.889dupC |
| AA Mutation | p.Arg297ProfsTer44(p.R297Pfs*44) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |