Primary Site >> Stomach Cancer
Gene >> RAD50
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000378823 |
| Start | 132595779:132595779(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs753002904 |
| CDS Mutation | c.2176C>T |
| AA Mutation | p.Arg726Cys(p.R726C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000378823 |
| Start | 132589823:132589823(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1438G>A |
| AA Mutation | p.Glu480Lys(p.E480K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000378823 |
| Start | 132637134:132637134(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3409A>G |
| AA Mutation | p.Ser1137Gly(p.S1137G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000378823 |
| Start | 132575795:132575795(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.232G>A |
| AA Mutation | p.Val78Met(p.V78M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000378823 |
| Start | 132638159:132638159(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs747603489 |
| CDS Mutation | c.3554G>A |
| AA Mutation | p.Arg1185Gln(p.R1185Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000378823 |
| Start | 132640773:132640773(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3720A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000378823 |
| Start | 132595646:132595646(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2043C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000378823 |
| Start | 132603432:132603432(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2340T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000378823 |
| Start | 132579367:132579367(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.418delA |
| AA Mutation | p.Met140Ter(p.M140*) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000378823 |
| Start | 132608690:132608690(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs758740142 |
| CDS Mutation | c.2801delA |
| AA Mutation | p.Asn934IlefsTer6(p.N934Ifs*6) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000378823 |
| Start | 132591958:132591958(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1722delA |
| AA Mutation | p.Lys574AsnfsTer24(p.K574Nfs*24) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000378823 |
| Start | 132618134:132618134(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs368980595 |
| CDS Mutation | c.3229C>T |
| AA Mutation | p.Arg1077Ter(p.R1077*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |