Primary Site >> Stomach Cancer
Gene >> ZSCAN18
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000240727 |
| Start | 58089954:58089954(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.314T>G |
| AA Mutation | p.Val105Gly(p.V105G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000240727 |
| Start | 58090110:58090110(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.158G>A |
| AA Mutation | p.Arg53Gln(p.R53Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000240727 |
| Start | 58088816:58088816(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs73058515 |
| CDS Mutation | c.425C>T |
| AA Mutation | p.Ala142Val(p.A142V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000240727 |
| Start | 58085206:58085206(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1012C>G |
| AA Mutation | p.Pro338Ala(p.P338A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000240727 |
| Start | 58090044:58090044(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.224G>A |
| AA Mutation | p.Arg75His(p.R75H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000240727 |
| Start | 58090248:58090248(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs376941867 |
| CDS Mutation | c.20C>T |
| AA Mutation | p.Ala7Val(p.A7V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000240727 |
| Start | 58090127:58090127(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.141C>A |
| AA Mutation | p.Phe47Leu(p.F47L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000240727 |
| Start | 58090111:58090111(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.157C>T |
| AA Mutation | p.Arg53Trp(p.R53W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000240727 |
| Start | 58085196:58085196(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1022C>T |
| AA Mutation | p.Ala341Val(p.A341V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000240727 |
| Start | 58086186:58086186(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs758047896 |
| CDS Mutation | c.826A>G |
| AA Mutation | p.Ser276Gly(p.S276G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000240727 |
| Start | 58090200:58090200(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs144951190 |
| CDS Mutation | c.68C>T |
| AA Mutation | p.Pro23Leu(p.P23L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000240727 |
| Start | 58085293:58085293(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.925C>A |
| AA Mutation | p.Pro309Thr(p.P309T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000240727 |
| Start | 58085096:58085096(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1122C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000240727 |
| Start | 58087337:58087337(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs375141880 |
| CDS Mutation | c.621C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000240727 |
| Start | 58085102:58085102(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1116G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000240727 |
| Start | 58085357:58085357(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.861C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000240727 |
| Start | 58090187:58090187(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs149865437 |
| CDS Mutation | c.81C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000240727 |
| Start | 58084786:58084786(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1432delC |
| AA Mutation | p.Gln478AsnfsTer49(p.Q478Nfs*49) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |