Primary Site >> Stomach Cancer
Gene >> FZD2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000315323 |
| Start | 44557974:44557974(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.286T>C |
| AA Mutation | p.Tyr96His(p.Y96H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000315323 |
| Start | 44559057:44559057(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1369C>T |
| AA Mutation | p.Arg457Trp(p.R457W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000315323 |
| Start | 44557947:44557947(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.259G>A |
| AA Mutation | p.Glu87Lys(p.E87K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000315323 |
| Start | 44559196:44559196(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs749932584 |
| CDS Mutation | c.1508C>T |
| AA Mutation | p.Ala503Val(p.A503V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000315323 |
| Start | 44559069:44559069(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1381C>T |
| AA Mutation | p.Arg461Cys(p.R461C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000315323 |
| Start | 44559162:44559162(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs751478883 |
| CDS Mutation | c.1474C>T |
| AA Mutation | p.Arg492Cys(p.R492C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000315323 |
| Start | 44559115:44559115(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1427T>A |
| AA Mutation | p.Val476Asp(p.V476D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000315323 |
| Start | 44559135:44559135(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1447G>A |
| AA Mutation | p.Glu483Lys(p.E483K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000315323 |
| Start | 44558444:44558444(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs773943647 |
| CDS Mutation | c.756G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000315323 |
| Start | 44559209:44559209(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs758721487 |
| CDS Mutation | c.1521G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000315323 |
| Start | 44558156:44558156(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.468C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000315323 |
| Start | 44558075:44558075(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.387T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000315323 |
| Start | 44559293:44559293(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1605G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000315323 |
| Start | 44558885:44558885(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1197C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000315323 |
| Start | 44559131:44559131(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1443C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000315323 |
| Start | 44559020:44559020(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1332C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000315323 |
| Start | 44559086:44559086(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs772686055 |
| CDS Mutation | c.1398C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |