Primary Site >> Stomach Cancer
Gene >> NLRP9
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000332836 |
| Start | 55711947:55711947(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs199518376 |
| CDS Mutation | c.2696G>A |
| AA Mutation | p.Arg899His(p.R899H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000332836 |
| Start | 55729898:55729898(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs758258759 |
| CDS Mutation | c.1927G>A |
| AA Mutation | p.Asp643Asn(p.D643N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000332836 |
| Start | 55715058:55715058(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2498T>G |
| AA Mutation | p.Leu833Arg(p.L833R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000332836 |
| Start | 55733462:55733462(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.369C>A |
| AA Mutation | p.Phe123Leu(p.F123L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000332836 |
| Start | 55724010:55724010(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2129A>G |
| AA Mutation | p.Lys710Arg(p.K710R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000332836 |
| Start | 55732555:55732555(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs751248353 |
| CDS Mutation | c.1276G>A |
| AA Mutation | p.Val426Met(p.V426M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000332836 |
| Start | 55732377:55732377(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1454A>G |
| AA Mutation | p.Gln485Arg(p.Q485R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000332836 |
| Start | 55716729:55716729(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2329A>G |
| AA Mutation | p.Met777Val(p.M777V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000332836 |
| Start | 55712493:55712493(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2599G>A |
| AA Mutation | p.Glu867Lys(p.E867K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000332836 |
| Start | 55732425:55732425(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1406C>T |
| AA Mutation | p.Ala469Val(p.A469V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000332836 |
| Start | 55732969:55732969(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs371355203 |
| CDS Mutation | c.862C>T |
| AA Mutation | p.Arg288Trp(p.R288W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000332836 |
| Start | 55732130:55732130(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1701A>C |
| AA Mutation | p.Glu567Asp(p.E567D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000332836 |
| Start | 55712426:55712426(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2666G>A |
| AA Mutation | p.Cys889Tyr(p.C889Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000332836 |
| Start | 55732966:55732966(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.865C>T |
| AA Mutation | p.His289Tyr(p.H289Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000332836 |
| Start | 55715117:55715117(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2439T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000332836 |
| Start | 55738171:55738171(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs370169487 |
| CDS Mutation | c.204A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000332836 |
| Start | 55732556:55732556(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1275C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000332836 |
| Start | 55732472:55732472(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs746903877 |
| CDS Mutation | c.1359C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000332836 |
| Start | 55733390:55733390(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.441T>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000332836 |
| Start | 55716813:55716813(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2245T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000332836 |
| Start | 55724036:55724036(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2103C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000332836 |
| Start | 55724057:55724057(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2082C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000332836 |
| Start | 55729977:55729977(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs376696951 |
| CDS Mutation | c.1848C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000332836 |
| Start | 55733040:55733040(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.791delA |
| AA Mutation | p.Lys264ArgfsTer12(p.K264Rfs*12) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 25 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000332836 |
| Start | 55738356:55738356(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.19delT |
| AA Mutation | p.Ser7ArgfsTer9(p.S7Rfs*9) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 26 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000332836 |
| Start | 55733179:55733179(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.652delT |
| AA Mutation | p.Ser218ProfsTer16(p.S218Pfs*16) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 27 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000332836 |
| Start | 55732483:55732483(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1348G>T |
| AA Mutation | p.Glu450Ter(p.E450*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 28 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000332836 |
| Start | 55708982:55708983(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | rs765623160 |
| CDS Mutation | c.2905dupA |
| AA Mutation | p.Ile969AsnfsTer13(p.I969Nfs*13) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |