Primary Site >> Stomach Cancer
Gene >> GAD1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000358196 |
| Start | 170844079:170844079(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.673A>G |
| AA Mutation | p.Met225Val(p.M225V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000358196 |
| Start | 170831111:170831111(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.466T>G |
| AA Mutation | p.Leu156Val(p.L156V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000358196 |
| Start | 170829506:170829506(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs138838552 |
| CDS Mutation | c.177G>T |
| AA Mutation | p.Glu59Asp(p.E59D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000358196 |
| Start | 170846063:170846063(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1002G>T |
| AA Mutation | p.Lys334Asn(p.K334N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000358196 |
| Start | 170845511:170845511(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.757G>A |
| AA Mutation | p.Ala253Thr(p.A253T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000358196 |
| Start | 170831109:170831109(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.464A>C |
| AA Mutation | p.Asn155Thr(p.N155T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000358196 |
| Start | 170844065:170844065(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.659C>T |
| AA Mutation | p.Pro220Leu(p.P220L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000358196 |
| Start | 170847768:170847768(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs188421952 |
| CDS Mutation | c.1095A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000358196 |
| Start | 170844063:170844063(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.657A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000358196 |
| Start | 170859747:170859747(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1650T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000358196 |
| Start | 170822091:170822091(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs774772554 |
| CDS Mutation | c.87C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000358196 |
| Start | 170818636:170818636(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs765913071 |
| CDS Mutation | c.45G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000358196 |
| Start | 170846013:170846013(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.955delA |
| AA Mutation | p.Ile319Ter(p.I319*) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |