Primary Site >> Stomach Cancer
Gene >> ALDH1L1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000393434 |
| Start | 126131467:126131467(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs368202745 |
| CDS Mutation | c.1540G>A |
| AA Mutation | p.Val514Ile(p.V514I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000393434 |
| Start | 126135548:126135548(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs755365962 |
| CDS Mutation | c.1459C>T |
| AA Mutation | p.Arg487Trp(p.R487W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000393434 |
| Start | 126154625:126154625(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.649G>A |
| AA Mutation | p.Ala217Thr(p.A217T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000393434 |
| Start | 126131475:126131475(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs768309358 |
| CDS Mutation | c.1532C>T |
| AA Mutation | p.Ala511Val(p.A511V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000393434 |
| Start | 126160925:126160925(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.55C>A |
| AA Mutation | p.Leu19Met(p.L19M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000393434 |
| Start | 126130226:126130226(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1691T>A |
| AA Mutation | p.Val564Asp(p.V564D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000393434 |
| Start | 126125663:126125663(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1753G>T |
| AA Mutation | p.Ala585Ser(p.A585S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000393434 |
| Start | 126135601:126135601(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1406A>C |
| AA Mutation | p.Lys469Thr(p.K469T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000393434 |
| Start | 126160975:126160975(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5A>C |
| AA Mutation | p.Lys2Thr(p.K2T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000393434 |
| Start | 126158472:126158472(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs754565747 |
| CDS Mutation | c.295C>T |
| AA Mutation | p.Arg99Trp(p.R99W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000393434 |
| Start | 126135560:126135560(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs747287426 |
| CDS Mutation | c.1447C>T |
| AA Mutation | p.Arg483Trp(p.R483W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000393434 |
| Start | 126105898:126105898(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2481C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000393434 |
| Start | 126131441:126131441(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs573922345 |
| CDS Mutation | c.1566C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000393434 |
| Start | 126131456:126131469(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1538_1551delCCGTCTACACGCTG |
| AA Mutation | p.Ala513GlyfsTer21(p.A513Gfs*21) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000393434 |
| Start | 126158472:126158472(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs768020555 |
| CDS Mutation | c.295delC |
| AA Mutation | p.Arg99GlyfsTer62(p.R99Gfs*62) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |