Primary Site >> Stomach Cancer
Gene >> AGBL2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000525123 |
| Start | 47710466:47710466(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs745526604 |
| CDS Mutation | c.143G>A |
| AA Mutation | p.Arg48Gln(p.R48Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000525123 |
| Start | 47690625:47690625(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1082A>G |
| AA Mutation | p.Lys361Arg(p.K361R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000525123 |
| Start | 47714641:47714641(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.10G>T |
| AA Mutation | p.Ala4Ser(p.A4S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000525123 |
| Start | 47690707:47690707(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1000G>C |
| AA Mutation | p.Val334Leu(p.V334L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000525123 |
| Start | 47710481:47710481(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs771276401 |
| CDS Mutation | c.128C>T |
| AA Mutation | p.Thr43Met(p.T43M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000525123 |
| Start | 47667609:47667609(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2302A>C |
| AA Mutation | p.Asn768His(p.N768H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000525123 |
| Start | 47660219:47660219(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2663C>T |
| AA Mutation | p.Ala888Val(p.A888V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000525123 |
| Start | 47660247:47660247(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2635A>G |
| AA Mutation | p.Arg879Gly(p.R879G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000525123 |
| Start | 47704654:47704654(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs777996137 |
| CDS Mutation | c.475C>T |
| AA Mutation | p.Arg159Cys(p.R159C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000525123 |
| Start | 47667602:47667602(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2309T>G |
| AA Mutation | p.Met770Arg(p.M770R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000525123 |
| Start | 47690743:47690743(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs778439327 |
| CDS Mutation | c.964A>G |
| AA Mutation | p.Ile322Val(p.I322V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000525123 |
| Start | 47690305:47690305(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1402G>T |
| AA Mutation | p.Gly468Cys(p.G468C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000525123 |
| Start | 47690408:47690408(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs759625602 |
| CDS Mutation | c.1299C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |