Primary Site >> Stomach Cancer
Gene >> ANO2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356134 |
| Start | 5830439:5830439(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs185666885 |
| CDS Mutation | c.827G>A |
| AA Mutation | p.Arg276His(p.R276H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356134 |
| Start | 5565587:5565587(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2701G>A |
| AA Mutation | p.Ala901Thr(p.A901T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356134 |
| Start | 5563462:5563462(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2837T>G |
| AA Mutation | p.Phe946Cys(p.F946C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356134 |
| Start | 5578504:5578504(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2251T>C |
| AA Mutation | p.Phe751Leu(p.F751L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356134 |
| Start | 5612713:5612713(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2033G>A |
| AA Mutation | p.Ser678Asn(p.S678N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356134 |
| Start | 5599609:5599609(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs199765638 |
| CDS Mutation | c.2111G>A |
| AA Mutation | p.Arg704Gln(p.R704Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356134 |
| Start | 5739380:5739380(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1362C>G |
| AA Mutation | p.Asn454Lys(p.N454K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356134 |
| Start | 5921198:5921198(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.364G>A |
| AA Mutation | p.Val122Ile(p.V122I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356134 |
| Start | 5921294:5921294(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.268G>A |
| AA Mutation | p.Asp90Asn(p.D90N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356134 |
| Start | 5635343:5635343(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1628C>T |
| AA Mutation | p.Ala543Val(p.A543V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356134 |
| Start | 5854080:5854080(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.584A>G |
| AA Mutation | p.Glu195Gly(p.E195G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356134 |
| Start | 5578396:5578396(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs761883684 |
| CDS Mutation | c.2359C>T |
| AA Mutation | p.Arg787Trp(p.R787W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356134 |
| Start | 5827802:5827802(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.850C>T |
| AA Mutation | p.Arg284Cys(p.R284C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356134 |
| Start | 5732563:5732563(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1505C>T |
| AA Mutation | p.Ala502Val(p.A502V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000356134 |
| Start | 5615275:5615275(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1842T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000356134 |
| Start | 5799551:5799551(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs376218931 |
| CDS Mutation | c.1002G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000356134 |
| Start | 5806070:5806070(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs571512821 |
| CDS Mutation | c.963C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000356134 |
| Start | 5599494:5599494(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2226C>A |
| AA Mutation | p.Tyr742Ter(p.Y742*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | splice_donor_variant |
| Transcription ID | ENST00000356134 |
| Start | 5578364:5578364(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs774207068 |
| CDS Mutation | c.2389+2T>C |
| Mutation Classification | Splice_Site |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | inframe_insertion |
| Transcription ID | ENST00000356134 |
| Start | 5575855:5575856(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.2594_2602dupCACAGTTTG |
| AA Mutation | p.Phe867_Asp868insAlaGlnPhe(p.F867_D868insAQF) |
| Mutation Classification | In_Frame_Ins |
| Feature Type | Transcript |