Primary Site >> Stomach Cancer
Gene >> PPP5C
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000012443 |
| Start | 46387185:46387185(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.997G>A |
| AA Mutation | p.Glu333Lys(p.E333K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000012443 |
| Start | 46353919:46353919(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.293G>A |
| AA Mutation | p.Gly98Asp(p.G98D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000012443 |
| Start | 46390097:46390097(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1402G>A |
| AA Mutation | p.Asp468Asn(p.D468N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000012443 |
| Start | 46353867:46353867(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.241G>A |
| AA Mutation | p.Ala81Thr(p.A81T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000012443 |
| Start | 46388679:46388679(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs767506672 |
| CDS Mutation | c.1303G>A |
| AA Mutation | p.Glu435Lys(p.E435K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000012443 |
| Start | 46387379:46387379(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1061G>A |
| AA Mutation | p.Gly354Asp(p.G354D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000012443 |
| Start | 46376473:46376473(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.532G>A |
| AA Mutation | p.Gly178Arg(p.G178R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000012443 |
| Start | 46383797:46383797(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.717A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000012443 |
| Start | 46353983:46353983(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.357C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000012443 |
| Start | 46383851:46383851(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs781056485 |
| CDS Mutation | c.771C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |