Primary Site >> Stomach Cancer
Gene >> PAK6
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000260404 |
| Start | 40272422:40272422(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs369825628 |
| CDS Mutation | c.1057C>T |
| AA Mutation | p.Arg353Cys(p.R353C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000260404 |
| Start | 40265960:40265960(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs778995699 |
| CDS Mutation | c.323G>A |
| AA Mutation | p.Arg108Gln(p.R108Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000260404 |
| Start | 40272444:40272444(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1079G>A |
| AA Mutation | p.Ser360Asn(p.S360N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000260404 |
| Start | 40272336:40272336(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs759202398 |
| CDS Mutation | c.971C>T |
| AA Mutation | p.Ser324Leu(p.S324L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000260404 |
| Start | 40273444:40273444(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1589A>G |
| AA Mutation | p.Asp530Gly(p.D530G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000260404 |
| Start | 40265851:40265851(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs777247289 |
| CDS Mutation | c.214C>T |
| AA Mutation | p.Arg72Trp(p.R72W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000260404 |
| Start | 40272932:40272932(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs34445577 |
| CDS Mutation | c.1423G>A |
| AA Mutation | p.Glu475Lys(p.E475K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000260404 |
| Start | 40264955:40264955(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs768438138 |
| CDS Mutation | c.170C>T |
| AA Mutation | p.Ser57Leu(p.S57L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000260404 |
| Start | 40273445:40273445(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1590C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000260404 |
| Start | 40276026:40276026(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1978C>T |
| AA Mutation | p.Gln660Ter(p.Q660*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |