Primary Site >> Stomach Cancer
Gene >> DLL1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000366756 |
| Start | 170290123:170290123(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.17C>T |
| AA Mutation | p.Ala6Val(p.A6V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000366756 |
| Start | 170283276:170283276(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2003A>C |
| AA Mutation | p.Gln668Pro(p.Q668P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000366756 |
| Start | 170283037:170283037(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs760189276 |
| CDS Mutation | c.2117C>T |
| AA Mutation | p.Ser706Leu(p.S706L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000366756 |
| Start | 170284984:170284984(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1184T>C |
| AA Mutation | p.Val395Ala(p.V395A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000366756 |
| Start | 170283311:170283311(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1968C>A |
| AA Mutation | p.Asp656Glu(p.D656E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000366756 |
| Start | 170288448:170288448(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.461C>T |
| AA Mutation | p.Thr154Met(p.T154M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000366756 |
| Start | 170285133:170285133(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1035T>A |
| AA Mutation | p.Asp345Glu(p.D345E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000366756 |
| Start | 170288472:170288472(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.437G>A |
| AA Mutation | p.Arg146His(p.R146H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000366756 |
| Start | 170288289:170288289(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.620G>A |
| AA Mutation | p.Arg207His(p.R207H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000366756 |
| Start | 170285012:170285012(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs372640222 |
| CDS Mutation | c.1156G>A |
| AA Mutation | p.Asp386Asn(p.D386N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000366756 |
| Start | 170288765:170288765(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.376G>A |
| AA Mutation | p.Ala126Thr(p.A126T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000366756 |
| Start | 170283366:170283366(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs780734657 |
| CDS Mutation | c.1913C>T |
| AA Mutation | p.Ala638Val(p.A638V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000366756 |
| Start | 170283665:170283665(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1614C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000366756 |
| Start | 170285052:170285052(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs757878599 |
| CDS Mutation | c.1116C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000366756 |
| Start | 170283767:170283767(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1512G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000366756 |
| Start | 170283072:170283072(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs753162814 |
| CDS Mutation | c.2082G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000366756 |
| Start | 170288378:170288378(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.531C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000366756 |
| Start | 170283449:170283449(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs778443720 |
| CDS Mutation | c.1830G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000366756 |
| Start | 170283075:170283075(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2079C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000366756 |
| Start | 170285586:170285586(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.845delG |
| AA Mutation | p.Gly282AlafsTer8(p.G282Afs*8) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000366756 |
| Start | 170283523:170283523(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.1756delG |
| AA Mutation | p.Glu586ArgfsTer5(p.E586Rfs*5) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000366756 |
| Start | 170283448:170283448(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1831C>T |
| AA Mutation | p.Gln611Ter(p.Q611*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000366756 |
| Start | 170285585:170285586(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | rs760008381 |
| CDS Mutation | c.845dupG |
| AA Mutation | p.Leu283ProfsTer14(p.L283Pfs*14) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |