Primary Site >> Stomach Cancer
Gene >> PPARGC1A
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264867 |
| Start | 23813927:23813927(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs765713824 |
| CDS Mutation | c.1556A>G |
| AA Mutation | p.Asp519Gly(p.D519G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264867 |
| Start | 23828489:23828489(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.668C>T |
| AA Mutation | p.Thr223Ile(p.T223I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264867 |
| Start | 23801766:23801766(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs748836875 |
| CDS Mutation | c.2257C>T |
| AA Mutation | p.Arg753Cys(p.R753C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264867 |
| Start | 23884874:23884874(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.112C>G |
| AA Mutation | p.Leu38Val(p.L38V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264867 |
| Start | 23813780:23813780(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs767722215 |
| CDS Mutation | c.1703G>A |
| AA Mutation | p.Arg568His(p.R568H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264867 |
| Start | 23812767:23812767(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1999A>G |
| AA Mutation | p.Arg667Gly(p.R667G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264867 |
| Start | 23814057:23814057(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs143142906 |
| CDS Mutation | c.1426G>A |
| AA Mutation | p.Asp476Asn(p.D476N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264867 |
| Start | 23831601:23831601(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.385C>T |
| AA Mutation | p.Pro129Ser(p.P129S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264867 |
| Start | 23828416:23828416(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.741G>C |
| AA Mutation | p.Gln247His(p.Q247H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000264867 |
| Start | 23829508:23829508(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.507T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000264867 |
| Start | 23828506:23828506(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs753811432 |
| CDS Mutation | c.651C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000264867 |
| Start | 23831638:23831638(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs529427617 |
| CDS Mutation | c.348C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |