Primary Site >> Stomach Cancer
Gene >> HCK
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000534862 |
| Start | 32086775:32086775(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.983C>T |
| AA Mutation | p.Pro328Leu(p.P328L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000534862 |
| Start | 32099075:32099075(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs555782474 |
| CDS Mutation | c.1318G>A |
| AA Mutation | p.Val440Ile(p.V440I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000534862 |
| Start | 32083944:32083944(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs765715998 |
| CDS Mutation | c.583G>A |
| AA Mutation | p.Val195Met(p.V195M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000534862 |
| Start | 32071682:32071682(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.83A>C |
| AA Mutation | p.Lys28Thr(p.K28T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000534862 |
| Start | 32101362:32101362(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1424G>A |
| AA Mutation | p.Arg475Gln(p.R475Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000534862 |
| Start | 32079824:32079824(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.479C>T |
| AA Mutation | p.Ala160Val(p.A160V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000534862 |
| Start | 32071666:32071666(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.67G>A |
| AA Mutation | p.Gly23Arg(p.G23R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000534862 |
| Start | 32084528:32084528(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.820G>A |
| AA Mutation | p.Gly274Arg(p.G274R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000534862 |
| Start | 32099116:32099116(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs75084400 |
| CDS Mutation | c.1359C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000534862 |
| Start | 32086761:32086761(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.969G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000534862 |
| Start | 32071728:32071728(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs780211762 |
| CDS Mutation | c.129C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000534862 |
| Start | 32101469:32101469(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1531C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000534862 |
| Start | 32084030:32084030(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs772900757 |
| CDS Mutation | c.669G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000534862 |
| Start | 32094006:32094006(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1236G>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000534862 |
| Start | 32083976:32083976(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.615C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000534862 |
| Start | 32083997:32083997(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.636C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000534862 |
| Start | 32099026:32099026(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1269G>A |
| AA Mutation | p.Trp423Ter(p.W423*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000534862 |
| Start | 32083998:32083998(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs144393224 |
| CDS Mutation | c.637C>T |
| AA Mutation | p.Arg213Ter(p.R213*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |