Primary Site >> Stomach Cancer
Gene >> SCNN1B
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000343070 |
| Start | 23371424:23371424(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200278167 |
| CDS Mutation | c.1006G>A |
| AA Mutation | p.Ala336Thr(p.A336T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000343070 |
| Start | 23380141:23380141(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs138784278 |
| CDS Mutation | c.1514G>A |
| AA Mutation | p.Arg505His(p.R505H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000343070 |
| Start | 23380514:23380514(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs112069765 |
| CDS Mutation | c.1636G>A |
| AA Mutation | p.Asp546Asn(p.D546N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000343070 |
| Start | 23355389:23355389(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.676A>G |
| AA Mutation | p.Ile226Val(p.I226V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000343070 |
| Start | 23371852:23371852(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1121A>G |
| AA Mutation | p.Tyr374Cys(p.Y374C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000343070 |
| Start | 23348622:23348622(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.23T>C |
| AA Mutation | p.Leu8Pro(p.L8P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000343070 |
| Start | 23377198:23377198(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1304C>T |
| AA Mutation | p.Ala435Val(p.A435V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000343070 |
| Start | 23348779:23348779(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs768826510 |
| CDS Mutation | c.180C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000343070 |
| Start | 23353008:23353008(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.519C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000343070 |
| Start | 23380574:23380574(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs137852704 |
| CDS Mutation | c.1696C>T |
| AA Mutation | p.Arg566Ter(p.R566*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |