Primary Site >> Stomach Cancer
Gene >> NLRP1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000572272 |
| Start | 5559822:5559822(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.874C>A |
| AA Mutation | p.Gln292Lys(p.Q292K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000572272 |
| Start | 5517862:5517862(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3941C>G |
| AA Mutation | p.Pro1314Arg(p.P1314R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000572272 |
| Start | 5539476:5539476(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs760487890 |
| CDS Mutation | c.2809G>A |
| AA Mutation | p.Val937Ile(p.V937I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000572272 |
| Start | 5582744:5582744(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs375872650 |
| CDS Mutation | c.374C>T |
| AA Mutation | p.Pro125Leu(p.P125L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000572272 |
| Start | 5553504:5553504(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2410C>A |
| AA Mutation | p.Leu804Ile(p.L804I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000572272 |
| Start | 5521772:5521772(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3535A>G |
| AA Mutation | p.Thr1179Ala(p.T1179A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000572272 |
| Start | 5539422:5539422(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs139267837 |
| CDS Mutation | c.2863C>T |
| AA Mutation | p.Arg955Cys(p.R955C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000572272 |
| Start | 5532849:5532849(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3269T>C |
| AA Mutation | p.Val1090Ala(p.V1090A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000572272 |
| Start | 5559276:5559276(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs202231072 |
| CDS Mutation | c.1420C>T |
| AA Mutation | p.Arg474Cys(p.R474C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000572272 |
| Start | 5533977:5533977(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2972T>C |
| AA Mutation | p.Val991Ala(p.V991A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000572272 |
| Start | 5539430:5539430(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2855A>G |
| AA Mutation | p.Lys952Arg(p.K952R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000572272 |
| Start | 5521632:5521632(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3675C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000572272 |
| Start | 5515048:5515048(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs199842944 |
| CDS Mutation | c.4128G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000572272 |
| Start | 5539471:5539471(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs772089891 |
| CDS Mutation | c.2814C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000572272 |
| Start | 5530695:5530695(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3306C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000572272 |
| Start | 5553550:5553550(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2364G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000572272 |
| Start | 5581956:5581956(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.555C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000572272 |
| Start | 5558728:5558728(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs139136010 |
| CDS Mutation | c.1968G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000572272 |
| Start | 5532944:5532944(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3174C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000572272 |
| Start | 5558948:5558948(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.1748delA |
| AA Mutation | p.Lys583ArgfsTer14(p.K583Rfs*14) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000572272 |
| Start | 5558732:5558732(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1964delA |
| AA Mutation | p.Lys655ArgfsTer3(p.K655Rfs*3) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000572272 |
| Start | 5559774:5559774(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs758319723 |
| CDS Mutation | c.922C>T |
| AA Mutation | p.Arg308Ter(p.R308*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |