Primary Site >> Stomach Cancer
Gene >> GPC6
| ID | 1 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000377047 |
| Start | 93830156:93830156(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs748831483 |
| CDS Mutation | c.322T>G |
| AA Mutation | p.Phe108Val(p.F108V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000377047 |
| Start | 93545410:93545410(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.308A>T |
| AA Mutation | p.Lys103Met(p.K103M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000377047 |
| Start | 94027787:94027787(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.770G>C |
| AA Mutation | p.Cys257Ser(p.C257S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000377047 |
| Start | 94286424:94286424(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.953A>G |
| AA Mutation | p.Lys318Arg(p.K318R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000377047 |
| Start | 93830471:93830471(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.637C>T |
| AA Mutation | p.Arg213Cys(p.R213C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000377047 |
| Start | 94382541:94382541(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1280G>T |
| AA Mutation | p.Ser427Ile(p.S427I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000377047 |
| Start | 93545385:93545385(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs760150200 |
| CDS Mutation | c.283C>T |
| AA Mutation | p.Arg95Cys(p.R95C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000377047 |
| Start | 94306048:94306048(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1077T>G |
| AA Mutation | p.Asn359Lys(p.N359K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000377047 |
| Start | 93227476:93227476(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.20C>T |
| AA Mutation | p.Ala7Val(p.A7V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000377047 |
| Start | 93830474:93830474(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs756656699 |
| CDS Mutation | c.640G>A |
| AA Mutation | p.Ala214Thr(p.A214T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000377047 |
| Start | 94398618:94398618(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1442A>T |
| AA Mutation | p.Asn481Ile(p.N481I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000377047 |
| Start | 94398488:94398488(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1312G>A |
| AA Mutation | p.Asp438Asn(p.D438N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000377047 |
| Start | 93227512:93227512(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.56T>C |
| AA Mutation | p.Leu19Pro(p.L19P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000377047 |
| Start | 93830441:93830441(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs376951709 |
| CDS Mutation | c.607G>A |
| AA Mutation | p.Val203Met(p.V203M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000377047 |
| Start | 94403087:94403087(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1538T>C |
| AA Mutation | p.Val513Ala(p.V513A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000377047 |
| Start | 93227539:93227539(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.83G>A |
| AA Mutation | p.Arg28Gln(p.R28Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000377047 |
| Start | 93227616:93227616(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.160G>A |
| AA Mutation | p.Gly54Arg(p.G54R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000377047 |
| Start | 93227496:93227496(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.40G>C |
| AA Mutation | p.Gly14Arg(p.G14R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000377047 |
| Start | 94306032:94306032(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs765293019 |
| CDS Mutation | c.1061G>A |
| AA Mutation | p.Arg354His(p.R354H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000377047 |
| Start | 94382494:94382494(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs368011430 |
| CDS Mutation | c.1233C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000377047 |
| Start | 94286454:94286454(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.986delA |
| AA Mutation | p.Asn329ThrfsTer60(p.N329Tfs*60) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |