Primary Site >> Stomach Cancer
Gene >> GOLPH3
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265070 |
| Start | 32135683:32135683(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.361A>G |
| AA Mutation | p.Ile121Val(p.I121V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265070 |
| Start | 32126231:32126231(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs760560885 |
| CDS Mutation | c.878T>C |
| AA Mutation | p.Val293Ala(p.V293A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265070 |
| Start | 32126475:32126475(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs779400964 |
| CDS Mutation | c.634C>T |
| AA Mutation | p.Arg212Cys(p.R212C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265070 |
| Start | 32126432:32126432(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.677T>G |
| AA Mutation | p.Val226Gly(p.V226G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265070 |
| Start | 32126474:32126474(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs374757542 |
| CDS Mutation | c.635G>A |
| AA Mutation | p.Arg212His(p.R212H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265070 |
| Start | 32126225:32126225(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs770704984 |
| CDS Mutation | c.884C>T |
| AA Mutation | p.Ala295Val(p.A295V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000265070 |
| Start | 32143770:32143770(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.336T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |