Primary Site >> Stomach Cancer
Gene >> DAXX
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000266000 |
| Start | 33321420:33321420(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs773142629 |
| CDS Mutation | c.355C>T |
| AA Mutation | p.Arg119Trp(p.R119W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000266000 |
| Start | 33319741:33319741(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1579A>G |
| AA Mutation | p.Ile527Val(p.I527V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000266000 |
| Start | 33319610:33319610(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1710G>T |
| AA Mutation | p.Glu570Asp(p.E570D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000266000 |
| Start | 33321491:33321491(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.284C>T |
| AA Mutation | p.Ala95Val(p.A95V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000266000 |
| Start | 33321096:33321096(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.679C>T |
| AA Mutation | p.Arg227Trp(p.R227W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000266000 |
| Start | 33320062:33320062(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1414G>A |
| AA Mutation | p.Glu472Lys(p.E472K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000266000 |
| Start | 33319705:33319705(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1615G>C |
| AA Mutation | p.Ala539Pro(p.A539P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000266000 |
| Start | 33320987:33320987(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.788G>A |
| AA Mutation | p.Arg263His(p.R263H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000266000 |
| Start | 33319743:33319743(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs141395832 |
| CDS Mutation | c.1577G>A |
| AA Mutation | p.Arg526His(p.R526H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000266000 |
| Start | 33320120:33320120(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1356A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000266000 |
| Start | 33320440:33320440(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1191G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000266000 |
| Start | 33319736:33319736(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1584G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000266000 |
| Start | 33321745:33321745(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.181C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000266000 |
| Start | 33320823:33320823(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs779014832 |
| CDS Mutation | c.952C>T |
| AA Mutation | p.Arg318Ter(p.R318*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |