Primary Site >> Stomach Cancer
Gene >> ACTN4
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000252699 |
| Start | 38717182:38717182(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1009G>A |
| AA Mutation | p.Asp337Asn(p.D337N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000252699 |
| Start | 38729392:38729392(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2696A>G |
| AA Mutation | p.Lys899Arg(p.K899R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000252699 |
| Start | 38700673:38700673(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs759055242 |
| CDS Mutation | c.236G>A |
| AA Mutation | p.Arg79Gln(p.R79Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000252699 |
| Start | 38717249:38717249(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1076C>T |
| AA Mutation | p.Thr359Met(p.T359M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000252699 |
| Start | 38727955:38727955(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs778422858 |
| CDS Mutation | c.2347G>A |
| AA Mutation | p.Gly783Arg(p.G783R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000252699 |
| Start | 38706112:38706112(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.553G>A |
| AA Mutation | p.Val185Met(p.V185M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000252699 |
| Start | 38727953:38727953(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2345G>A |
| AA Mutation | p.Gly782Asp(p.G782D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000252699 |
| Start | 38728013:38728013(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2405A>C |
| AA Mutation | p.Glu802Ala(p.E802A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000252699 |
| Start | 38729125:38729125(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs376869655 |
| CDS Mutation | c.2548G>A |
| AA Mutation | p.Ala850Thr(p.A850T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000252699 |
| Start | 38724197:38724197(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1733C>T |
| AA Mutation | p.Pro578Leu(p.P578L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000252699 |
| Start | 38717191:38717191(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs760523958 |
| CDS Mutation | c.1018C>T |
| AA Mutation | p.Arg340Cys(p.R340C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000252699 |
| Start | 38723991:38723991(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs372902386 |
| CDS Mutation | c.1606C>T |
| AA Mutation | p.Arg536Cys(p.R536C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000252699 |
| Start | 38717301:38717301(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1128G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000252699 |
| Start | 38724440:38724440(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1885C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000252699 |
| Start | 38729405:38729405(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs760996008 |
| CDS Mutation | c.2709G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000252699 |
| Start | 38717280:38717280(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1107G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000252699 |
| Start | 38723680:38723680(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs750084549 |
| CDS Mutation | c.1509C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000252699 |
| Start | 38724303:38724303(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1839C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000252699 |
| Start | 38709427:38709427(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs763760070 |
| CDS Mutation | c.684C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |