Primary Site >> Stomach Cancer
Gene >> ANO3
| ID | 1 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000256737 |
| Start | 26660262:26660262(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2764C>T |
| AA Mutation | p.His922Tyr(p.H922Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000256737 |
| Start | 26656186:26656186(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2638G>A |
| AA Mutation | p.Gly880Arg(p.G880R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000256737 |
| Start | 26643301:26643301(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2395C>T |
| AA Mutation | p.Arg799Trp(p.R799W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000256737 |
| Start | 26598919:26598919(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1592C>T |
| AA Mutation | p.Thr531Met(p.T531M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000256737 |
| Start | 26537412:26537412(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.983G>A |
| AA Mutation | p.Arg328His(p.R328H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000256737 |
| Start | 26598868:26598868(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs199929076 |
| CDS Mutation | c.1541G>A |
| AA Mutation | p.Arg514His(p.R514H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000256737 |
| Start | 26656392:26656392(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2674G>T |
| AA Mutation | p.Gly892Cys(p.G892C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000256737 |
| Start | 26531303:26531303(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs767545047 |
| CDS Mutation | c.836A>C |
| AA Mutation | p.Tyr279Ser(p.Y279S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000256737 |
| Start | 26542026:26542026(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs187173978 |
| CDS Mutation | c.1112G>A |
| AA Mutation | p.Arg371His(p.R371H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000256737 |
| Start | 26656161:26656161(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2613C>A |
| AA Mutation | p.Phe871Leu(p.F871L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000256737 |
| Start | 26634212:26634212(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1882C>G |
| AA Mutation | p.Arg628Gly(p.R628G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000256737 |
| Start | 26635045:26635045(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2018T>G |
| AA Mutation | p.Leu673Arg(p.L673R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000256737 |
| Start | 26531320:26531320(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs745681189 |
| CDS Mutation | c.853C>T |
| AA Mutation | p.Arg285Cys(p.R285C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000256737 |
| Start | 26531326:26531326(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs779890833 |
| CDS Mutation | c.859C>T |
| AA Mutation | p.Arg287Trp(p.R287W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000256737 |
| Start | 26660377:26660377(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2879C>T |
| AA Mutation | p.Ala960Val(p.A960V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000256737 |
| Start | 26559730:26559730(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1398G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000256737 |
| Start | 26516907:26516907(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.672G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000256737 |
| Start | 26534531:26534531(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200828579 |
| CDS Mutation | c.945C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |