Primary Site >> Stomach Cancer
Gene >> HAUS3
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000243706 |
| Start | 2238758:2238758(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs148548454 |
| CDS Mutation | c.1195C>T |
| AA Mutation | p.Arg399Trp(p.R399W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000243706 |
| Start | 2240906:2240906(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.41T>A |
| AA Mutation | p.Ile14Asn(p.I14N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000243706 |
| Start | 2232058:2232058(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1681G>T |
| AA Mutation | p.Ala561Ser(p.A561S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000243706 |
| Start | 2238668:2238668(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1285C>A |
| AA Mutation | p.Pro429Thr(p.P429T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000243706 |
| Start | 2240540:2240540(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.407G>C |
| AA Mutation | p.Arg136Thr(p.R136T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000243706 |
| Start | 2240323:2240323(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.624G>C |
| AA Mutation | p.Glu208Asp(p.E208D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000243706 |
| Start | 2232084:2232084(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs574720440 |
| CDS Mutation | c.1655A>T |
| AA Mutation | p.Asp552Val(p.D552V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000243706 |
| Start | 2238999:2238999(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.954C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000243706 |
| Start | 2240907:2240907(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs748396956 |
| CDS Mutation | c.40delA |
| AA Mutation | p.Ile14LeufsTer27(p.I14Lfs*27) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |