Primary Site >> Stomach Cancer
Gene >> ABHD2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000352732 |
| Start | 89195266:89195266(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1121G>T |
| AA Mutation | p.Gly374Val(p.G374V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000352732 |
| Start | 89155462:89155462(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs748725026 |
| CDS Mutation | c.466C>T |
| AA Mutation | p.Arg156Trp(p.R156W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000352732 |
| Start | 89175886:89175886(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.613G>T |
| AA Mutation | p.Gly205Cys(p.G205C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000352732 |
| Start | 89155468:89155468(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs778316032 |
| CDS Mutation | c.472G>A |
| AA Mutation | p.Ala158Thr(p.A158T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000352732 |
| Start | 89175963:89175963(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs763642629 |
| CDS Mutation | c.690C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000352732 |
| Start | 89175879:89175879(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.606C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000352732 |
| Start | 89193270:89193270(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs74029947 |
| CDS Mutation | c.1032C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000352732 |
| Start | 89155467:89155467(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs559362885 |
| CDS Mutation | c.471C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000352732 |
| Start | 89151697:89151697(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.219delG |
| AA Mutation | p.Ser75ValfsTer15(p.S75Vfs*15) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |