Primary Site >> Stomach Cancer
Gene >> ANO4
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000392977 |
| Start | 101040064:101040064(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1007T>C |
| AA Mutation | p.Leu336Ser(p.L336S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000392977 |
| Start | 101127005:101127005(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs139827573 |
| CDS Mutation | c.2803C>T |
| AA Mutation | p.Arg935Cys(p.R935C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000392977 |
| Start | 101037134:101037134(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.881C>T |
| AA Mutation | p.Ala294Val(p.A294V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000392977 |
| Start | 101111572:101111572(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2312A>G |
| AA Mutation | p.Tyr771Cys(p.Y771C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000392977 |
| Start | 100942509:100942509(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.430G>T |
| AA Mutation | p.Ala144Ser(p.A144S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000392977 |
| Start | 100987564:100987564(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs372521580 |
| CDS Mutation | c.628C>T |
| AA Mutation | p.Arg210Trp(p.R210W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000392977 |
| Start | 100974868:100974868(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs752635853 |
| CDS Mutation | c.581G>A |
| AA Mutation | p.Arg194His(p.R194H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000392977 |
| Start | 101096631:101096631(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1834G>A |
| AA Mutation | p.Ala612Thr(p.A612T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000392977 |
| Start | 101111629:101111629(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs763712389 |
| CDS Mutation | c.2369C>T |
| AA Mutation | p.Ala790Val(p.A790V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000392977 |
| Start | 100942521:100942521(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs746948652 |
| CDS Mutation | c.442C>A |
| AA Mutation | p.Gln148Lys(p.Q148K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000392977 |
| Start | 101086742:101086742(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1619C>T |
| AA Mutation | p.Ala540Val(p.A540V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000392977 |
| Start | 101099706:101099706(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2135A>G |
| AA Mutation | p.Glu712Gly(p.E712G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000392977 |
| Start | 101094272:101094272(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1718C>T |
| AA Mutation | p.Ala573Val(p.A573V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000392977 |
| Start | 101048400:101048400(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1311G>C |
| AA Mutation | p.Trp437Cys(p.W437C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000392977 |
| Start | 101039986:101039986(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.929C>T |
| AA Mutation | p.Thr310Ile(p.T310I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000392977 |
| Start | 100987607:100987607(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.671C>T |
| AA Mutation | p.Thr224Ile(p.T224I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000392977 |
| Start | 101116741:101116741(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2513G>T |
| AA Mutation | p.Arg838Leu(p.R838L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000392977 |
| Start | 101083723:101083723(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs765804915 |
| CDS Mutation | c.1441C>T |
| AA Mutation | p.Arg481Trp(p.R481W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000392977 |
| Start | 100942501:100942501(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.422A>G |
| AA Mutation | p.Asn141Ser(p.N141S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000392977 |
| Start | 100939318:100939318(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.164C>T |
| AA Mutation | p.Ala55Val(p.A55V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000392977 |
| Start | 101043596:101043596(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1212T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000392977 |
| Start | 101110456:101110456(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2202A>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000392977 |
| Start | 101042451:101042451(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1137G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000392977 |
| Start | 101127058:101127058(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs750104788 |
| CDS Mutation | c.2856C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 25 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000392977 |
| Start | 100939443:100939443(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.293delG |
| AA Mutation | p.Gly98GlufsTer58(p.G98Efs*58) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 26 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000392977 |
| Start | 100901818:100901818(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.37delA |
| AA Mutation | p.Thr13ProfsTer53(p.T13Pfs*53) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 27 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000392977 |
| Start | 101083687:101083687(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs775993661 |
| CDS Mutation | c.1405C>T |
| AA Mutation | p.Arg469Ter(p.R469*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 28 |
| Mutation Consequence | inframe_deletion |
| Transcription ID | ENST00000392977 |
| Start | 101120559:101120567(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.2611_2619delTATGGCTAC |
| AA Mutation | p.Tyr871_Tyr873del(p.Y871_Y873del) |
| Mutation Classification | In_Frame_Del |
| Feature Type | Transcript |