Primary Site >> Stomach Cancer
Gene >> ANO6
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000320560 |
| Start | 45409382:45409382(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1906T>C |
| AA Mutation | p.Phe636Leu(p.F636L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000320560 |
| Start | 45423031:45423031(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2495C>T |
| AA Mutation | p.Ala832Val(p.A832V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000320560 |
| Start | 45429108:45429108(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs773140175 |
| CDS Mutation | c.2530G>A |
| AA Mutation | p.Val844Ile(p.V844I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000320560 |
| Start | 45429206:45429206(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2628G>T |
| AA Mutation | p.Lys876Asn(p.K876N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000320560 |
| Start | 45347040:45347040(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs745465915 |
| CDS Mutation | c.298G>A |
| AA Mutation | p.Glu100Lys(p.E100K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000320560 |
| Start | 45390479:45390479(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1367C>T |
| AA Mutation | p.Ala456Val(p.A456V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000320560 |
| Start | 45416767:45416767(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2080A>G |
| AA Mutation | p.Asn694Asp(p.N694D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000320560 |
| Start | 45347085:45347085(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.343T>C |
| AA Mutation | p.Ser115Pro(p.S115P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000320560 |
| Start | 45403232:45403232(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1773A>C |
| AA Mutation | p.Arg591Ser(p.R591S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000320560 |
| Start | 45390466:45390466(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1354A>G |
| AA Mutation | p.Ile452Val(p.I452V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000320560 |
| Start | 45403486:45403486(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1830A>G |
| AA Mutation | p.Ile610Met(p.I610M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000320560 |
| Start | 45421120:45421120(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2267A>G |
| AA Mutation | p.Tyr756Cys(p.Y756C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000320560 |
| Start | 45429142:45429142(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2564C>T |
| AA Mutation | p.Ala855Val(p.A855V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000320560 |
| Start | 45378094:45378094(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1146A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000320560 |
| Start | 45429122:45429122(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2544G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000320560 |
| Start | 45348063:45348063(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs144883809 |
| CDS Mutation | c.381C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000320560 |
| Start | 45401932:45401932(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs752518869 |
| CDS Mutation | c.1524G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | splice_donor_variant;coding_sequence_variant;intron_variant |
| Transcription ID | ENST00000320560 |
| Start | 45348623:45348644(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.740_747+14delTCCATGATGTAAGTTAAAAGGC |
| Mutation Classification | Splice_Site |
| Feature Type | Transcript |