Primary Site >> Stomach Cancer
Gene >> MAD1L1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265854 |
| Start | 2069241:2069241(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1171G>A |
| AA Mutation | p.Glu391Lys(p.E391K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265854 |
| Start | 1816086:1816086(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2141G>A |
| AA Mutation | p.Arg714His(p.R714H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000265854 |
| Start | 1957631:1957631(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1594C>G |
| AA Mutation | p.Gln532Glu(p.Q532E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265854 |
| Start | 1957643:1957643(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs747276194 |
| CDS Mutation | c.1582C>T |
| AA Mutation | p.Arg528Trp(p.R528W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265854 |
| Start | 2222720:2222720(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs374334107 |
| CDS Mutation | c.326G>A |
| AA Mutation | p.Arg109His(p.R109H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265854 |
| Start | 1898216:1898216(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1982A>G |
| AA Mutation | p.Asp661Gly(p.D661G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265854 |
| Start | 1898219:1898219(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1979G>T |
| AA Mutation | p.Gly660Val(p.G660V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265854 |
| Start | 2002091:2002091(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1390G>A |
| AA Mutation | p.Gly464Arg(p.G464R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265854 |
| Start | 1957654:1957654(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1571C>T |
| AA Mutation | p.Ala524Val(p.A524V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000265854 |
| Start | 2014586:2014586(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1275C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000265854 |
| Start | 1898347:1898347(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201332815 |
| CDS Mutation | c.1851G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000265854 |
| Start | 2216165:2216165(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs535463953 |
| CDS Mutation | c.801G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000265854 |
| Start | 2222737:2222737(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.309C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000265854 |
| Start | 2216279:2216279(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs749822499 |
| CDS Mutation | c.687G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000265854 |
| Start | 1936778:1936778(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs571940655 |
| CDS Mutation | c.1716C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000265854 |
| Start | 2069242:2069242(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs746787094 |
| CDS Mutation | c.1170C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |