Primary Site >> Stomach Cancer
Gene >> PPP2R1A
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000322088 |
| Start | 52220231:52220231(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1345G>A |
| AA Mutation | p.Ala449Thr(p.A449T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000322088 |
| Start | 52212964:52212964(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.661C>T |
| AA Mutation | p.Arg221Trp(p.R221W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000322088 |
| Start | 52212997:52212997(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs769334090 |
| CDS Mutation | c.694G>A |
| AA Mutation | p.Ala232Thr(p.A232T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000322088 |
| Start | 52212726:52212726(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs786205227 |
| CDS Mutation | c.544C>T |
| AA Mutation | p.Arg182Trp(p.R182W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000322088 |
| Start | 52216541:52216541(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1006G>A |
| AA Mutation | p.Asp336Asn(p.D336N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000322088 |
| Start | 52211273:52211273(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs148604195 |
| CDS Mutation | c.284C>T |
| AA Mutation | p.Ser95Leu(p.S95L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000322088 |
| Start | 52212730:52212730(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.548G>A |
| AA Mutation | p.Arg183Gln(p.R183Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000322088 |
| Start | 52221011:52221011(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1396C>A |
| AA Mutation | p.Leu466Met(p.L466M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000322088 |
| Start | 52212765:52212765(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.583G>A |
| AA Mutation | p.Val195Met(p.V195M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000322088 |
| Start | 52211452:52211452(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.463T>A |
| AA Mutation | p.Tyr155Asn(p.Y155N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000322088 |
| Start | 52215796:52215796(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.825G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000322088 |
| Start | 52201979:52201979(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs775159886 |
| CDS Mutation | c.114C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000322088 |
| Start | 52219705:52219705(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1143G>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000322088 |
| Start | 52211367:52211367(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs199586303 |
| CDS Mutation | c.378G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |