Primary Site >> Stomach Cancer
Gene >> INPPL1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000298229 |
| Start | 72228216:72228216(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.209G>A |
| AA Mutation | p.Arg70His(p.R70H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000298229 |
| Start | 72237477:72237477(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs750607140 |
| CDS Mutation | c.3233G>A |
| AA Mutation | p.Arg1078Gln(p.R1078Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000298229 |
| Start | 72230998:72230998(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs758142583 |
| CDS Mutation | c.1306G>A |
| AA Mutation | p.Val436Ile(p.V436I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000298229 |
| Start | 72231131:72231131(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1439A>G |
| AA Mutation | p.Glu480Gly(p.E480G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000298229 |
| Start | 72231574:72231574(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1574T>C |
| AA Mutation | p.Val525Ala(p.V525A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000298229 |
| Start | 72235920:72235920(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs144622174 |
| CDS Mutation | c.2813C>T |
| AA Mutation | p.Pro938Leu(p.P938L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000298229 |
| Start | 72228370:72228370(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs762663532 |
| CDS Mutation | c.269G>A |
| AA Mutation | p.Arg90His(p.R90H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000298229 |
| Start | 72228210:72228210(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.203C>T |
| AA Mutation | p.Thr68Met(p.T68M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000298229 |
| Start | 72228757:72228757(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs781357595 |
| CDS Mutation | c.428C>T |
| AA Mutation | p.Pro143Leu(p.P143L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000298229 |
| Start | 72237675:72237675(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs778488376 |
| CDS Mutation | c.3431C>T |
| AA Mutation | p.Ala1144Val(p.A1144V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000298229 |
| Start | 72235189:72235189(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2489G>A |
| AA Mutation | p.Gly830Asp(p.G830D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000298229 |
| Start | 72232944:72232944(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1921C>T |
| AA Mutation | p.Arg641Trp(p.R641W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000298229 |
| Start | 72237423:72237423(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3179A>T |
| AA Mutation | p.Asp1060Val(p.D1060V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000298229 |
| Start | 72231136:72231136(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1444C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000298229 |
| Start | 72237283:72237283(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3039C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000298229 |
| Start | 72235712:72235712(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2697G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000298229 |
| Start | 72237166:72237166(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200100388 |
| CDS Mutation | c.2922C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000298229 |
| Start | 72237165:72237165(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.2927delC |
| AA Mutation | p.Pro976HisfsTer155(p.P976Hfs*155) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000298229 |
| Start | 72237440:72237440(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.3201delC |
| AA Mutation | p.Ser1068AlafsTer63(p.S1068Afs*63) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000298229 |
| Start | 72235720:72235720(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.2709delC |
| AA Mutation | p.Ser904LeufsTer54(p.S904Lfs*54) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000298229 |
| Start | 72237704:72237704(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs764259451 |
| CDS Mutation | c.3466delC |
| AA Mutation | p.Arg1156GlyfsTer46(p.R1156Gfs*46) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | splice_donor_variant |
| Transcription ID | ENST00000298229 |
| Start | 72231191:72231191(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1497+2T>C |
| Mutation Classification | Splice_Site |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | inframe_deletion |
| Transcription ID | ENST00000298229 |
| Start | 72233088:72233090(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs746559845 |
| CDS Mutation | c.1967_1969delCCT |
| AA Mutation | p.Ser656del(p.S656del) |
| Mutation Classification | In_Frame_Del |
| Feature Type | Transcript |