Primary Site >> Stomach Cancer
Gene >> KCNA5
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000252321 |
| Start | 5045766:5045766(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1619G>A |
| AA Mutation | p.Gly540Asp(p.G540D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000252321 |
| Start | 5045720:5045720(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs376656991 |
| CDS Mutation | c.1573C>T |
| AA Mutation | p.Arg525Trp(p.R525W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000252321 |
| Start | 5045391:5045391(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs753084398 |
| CDS Mutation | c.1244G>A |
| AA Mutation | p.Arg415His(p.R415H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000252321 |
| Start | 5045581:5045581(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1434G>A |
| AA Mutation | p.Met478Ile(p.M478I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000252321 |
| Start | 5044833:5044833(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs747143051 |
| CDS Mutation | c.686G>A |
| AA Mutation | p.Arg229His(p.R229H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000252321 |
| Start | 5044653:5044653(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.506G>A |
| AA Mutation | p.Arg169Gln(p.R169Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000252321 |
| Start | 5045126:5045126(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.979G>A |
| AA Mutation | p.Val327Met(p.V327M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000252321 |
| Start | 5044737:5044737(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.590C>T |
| AA Mutation | p.Ala197Val(p.A197V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000252321 |
| Start | 5044964:5044964(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.817C>T |
| AA Mutation | p.Pro273Ser(p.P273S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000252321 |
| Start | 5045007:5045007(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs144246051 |
| CDS Mutation | c.860C>T |
| AA Mutation | p.Ala287Val(p.A287V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000252321 |
| Start | 5045245:5045245(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1098C>A |
| AA Mutation | p.Phe366Leu(p.F366L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000252321 |
| Start | 5045021:5045021(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.874C>T |
| AA Mutation | p.Pro292Ser(p.P292S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000252321 |
| Start | 5044914:5044914(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.767C>G |
| AA Mutation | p.Ser256Trp(p.S256W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000252321 |
| Start | 5044503:5044503(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.356A>G |
| AA Mutation | p.His119Arg(p.H119R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000252321 |
| Start | 5045390:5045390(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1243C>T |
| AA Mutation | p.Arg415Cys(p.R415C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000252321 |
| Start | 5045972:5045972(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1825C>T |
| AA Mutation | p.Arg609Trp(p.R609W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000252321 |
| Start | 5045024:5045024(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.877G>A |
| AA Mutation | p.Ala293Thr(p.A293T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000252321 |
| Start | 5044629:5044629(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.482A>G |
| AA Mutation | p.Asn161Ser(p.N161S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000252321 |
| Start | 5044746:5044746(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.599T>C |
| AA Mutation | p.Ile200Thr(p.I200T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000252321 |
| Start | 5044848:5044848(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.701G>A |
| AA Mutation | p.Arg234His(p.R234H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000252321 |
| Start | 5045608:5045608(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1461G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000252321 |
| Start | 5045641:5045641(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs576837393 |
| CDS Mutation | c.1494G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |