Primary Site >> Stomach Cancer
Gene >> KCNA3
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369769 |
| Start | 110674106:110674106(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.704G>A |
| AA Mutation | p.Gly235Asp(p.G235D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369769 |
| Start | 110673515:110673515(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1295C>T |
| AA Mutation | p.Pro432Leu(p.P432L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369769 |
| Start | 110673213:110673213(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1597G>A |
| AA Mutation | p.Glu533Lys(p.E533K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369769 |
| Start | 110673935:110673935(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.875C>G |
| AA Mutation | p.Ser292Cys(p.S292C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369769 |
| Start | 110674431:110674431(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.379G>A |
| AA Mutation | p.Glu127Lys(p.E127K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369769 |
| Start | 110673842:110673842(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.968T>G |
| AA Mutation | p.Phe323Cys(p.F323C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369769 |
| Start | 110673263:110673263(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1547G>A |
| AA Mutation | p.Arg516Gln(p.R516Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369769 |
| Start | 110673873:110673873(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.937C>T |
| AA Mutation | p.Arg313Trp(p.R313W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369769 |
| Start | 110674316:110674316(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.494C>A |
| AA Mutation | p.Ser165Tyr(p.S165Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369769 |
| Start | 110674172:110674172(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.638G>A |
| AA Mutation | p.Arg213His(p.R213H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369769 |
| Start | 110674403:110674403(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.407G>A |
| AA Mutation | p.Arg136His(p.R136H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369769 |
| Start | 110674041:110674041(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.769C>T |
| AA Mutation | p.Pro257Ser(p.P257S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369769 |
| Start | 110673488:110673488(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1322C>G |
| AA Mutation | p.Thr441Ser(p.T441S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369769 |
| Start | 110674427:110674427(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.383C>T |
| AA Mutation | p.Thr128Met(p.T128M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369769 |
| Start | 110674197:110674197(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs764269530 |
| CDS Mutation | c.613C>T |
| AA Mutation | p.Arg205Trp(p.R205W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369769 |
| Start | 110674109:110674109(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.701G>A |
| AA Mutation | p.Arg234Gln(p.R234Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369769 |
| Start | 110673566:110673566(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1244C>T |
| AA Mutation | p.Ala415Val(p.A415V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369769 |
| Start | 110674185:110674185(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.625C>T |
| AA Mutation | p.Arg209Trp(p.R209W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000369769 |
| Start | 110674687:110674687(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.123G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000369769 |
| Start | 110674090:110674090(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.720C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000369769 |
| Start | 110673322:110673322(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1488A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000369769 |
| Start | 110674561:110674561(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.249C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000369769 |
| Start | 110674465:110674465(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.345C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000369769 |
| Start | 110673568:110673568(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1242C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 25 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000369769 |
| Start | 110673766:110673766(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs756328280 |
| CDS Mutation | c.1044C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 26 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000369769 |
| Start | 110673466:110673466(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1344C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 27 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000369769 |
| Start | 110674441:110674441(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.369C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 28 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000369769 |
| Start | 110674339:110674339(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs767302571 |
| CDS Mutation | c.471C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 29 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000369769 |
| Start | 110674309:110674309(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.501C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 30 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000369769 |
| Start | 110673520:110673520(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1290C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 31 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000369769 |
| Start | 110673649:110673649(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1161C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 32 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000369769 |
| Start | 110673631:110673631(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201922702 |
| CDS Mutation | c.1179G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |