Primary Site >> Stomach Cancer
Gene >> ALDH1B1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000377698 |
| Start | 38395866:38395866(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.118T>C |
| AA Mutation | p.Phe40Leu(p.F40L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000377698 |
| Start | 38395797:38395797(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs369090946 |
| CDS Mutation | c.49G>A |
| AA Mutation | p.Ala17Thr(p.A17T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000377698 |
| Start | 38395771:38395771(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs61757680 |
| CDS Mutation | c.23G>A |
| AA Mutation | p.Arg8Gln(p.R8Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000377698 |
| Start | 38396545:38396545(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.797T>C |
| AA Mutation | p.Val266Ala(p.V266A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000377698 |
| Start | 38396268:38396268(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs770082110 |
| CDS Mutation | c.520G>A |
| AA Mutation | p.Glu174Lys(p.E174K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000377698 |
| Start | 38396496:38396496(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs770868005 |
| CDS Mutation | c.748G>A |
| AA Mutation | p.Ala250Thr(p.A250T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000377698 |
| Start | 38396307:38396307(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.559T>G |
| AA Mutation | p.Phe187Val(p.F187V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000377698 |
| Start | 38397144:38397144(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs750694017 |
| CDS Mutation | c.1396G>A |
| AA Mutation | p.Gly466Arg(p.G466R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000377698 |
| Start | 38396882:38396882(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1134G>T |
| AA Mutation | p.Gln378His(p.Q378H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000377698 |
| Start | 38397272:38397272(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1524C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000377698 |
| Start | 38396153:38396153(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs772311325 |
| CDS Mutation | c.405C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000377698 |
| Start | 38397188:38397188(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs753782421 |
| CDS Mutation | c.1440G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000377698 |
| Start | 38396389:38396389(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.646delC |
| AA Mutation | p.Leu216SerfsTer20(p.L216Sfs*20) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |