Primary Site >> Stomach Cancer
Gene >> ALDH1A3
| ID | 1 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000329841 |
| Start | 100907123:100907123(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1236T>G |
| AA Mutation | p.Ile412Met(p.I412M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000329841 |
| Start | 100905580:100905580(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1126G>A |
| AA Mutation | p.Gly376Arg(p.G376R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000329841 |
| Start | 100900752:100900752(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1061G>T |
| AA Mutation | p.Gly354Val(p.G354V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000329841 |
| Start | 100892603:100892603(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.439T>C |
| AA Mutation | p.Trp147Arg(p.W147R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000329841 |
| Start | 100893975:100893975(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.559C>A |
| AA Mutation | p.Leu187Met(p.L187M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000329841 |
| Start | 100898132:100898132(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.830T>A |
| AA Mutation | p.Val277Glu(p.V277E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000329841 |
| Start | 100893960:100893960(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs747235458 |
| CDS Mutation | c.544T>G |
| AA Mutation | p.Phe182Val(p.F182V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000329841 |
| Start | 100905597:100905597(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs113661159 |
| CDS Mutation | c.1143C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000329841 |
| Start | 100892955:100892955(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs772326662 |
| CDS Mutation | c.486C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000329841 |
| Start | 100894052:100894052(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs149815923 |
| CDS Mutation | c.636C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |