Primary Site >> Stomach Cancer
Gene >> GAD2
| ID | 1 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000259271 |
| Start | 26281087:26281087(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1236G>T |
| AA Mutation | p.Glu412Asp(p.E412D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000259271 |
| Start | 26217907:26217907(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.202G>A |
| AA Mutation | p.Ala68Thr(p.A68T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000259271 |
| Start | 26224651:26224651(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.724G>A |
| AA Mutation | p.Gly242Ser(p.G242S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000259271 |
| Start | 26286456:26286456(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs369617935 |
| CDS Mutation | c.1348G>A |
| AA Mutation | p.Val450Ile(p.V450I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000259271 |
| Start | 26269132:26269132(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.934C>T |
| AA Mutation | p.Pro312Ser(p.P312S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000259271 |
| Start | 26219160:26219160(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.404T>C |
| AA Mutation | p.Phe135Ser(p.F135S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000259271 |
| Start | 26292484:26292484(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1406C>T |
| AA Mutation | p.Ala469Val(p.A469V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000259271 |
| Start | 26270641:26270641(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.977G>A |
| AA Mutation | p.Gly326Glu(p.G326E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000259271 |
| Start | 26217669:26217669(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs754627728 |
| CDS Mutation | c.136G>A |
| AA Mutation | p.Ala46Thr(p.A46T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000259271 |
| Start | 26217658:26217658(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.125A>C |
| AA Mutation | p.Asn42Thr(p.N42T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000259271 |
| Start | 26216824:26216824(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201811839 |
| CDS Mutation | c.15C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000259271 |
| Start | 26286446:26286446(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs760375732 |
| CDS Mutation | c.1338C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000259271 |
| Start | 26217852:26217852(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs768975616 |
| CDS Mutation | c.147C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |