Primary Site >> Stomach Cancer
Gene >> NLRP12
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000324134 |
| Start | 53796001:53796001(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2956G>T |
| AA Mutation | p.Ala986Ser(p.A986S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000324134 |
| Start | 53798274:53798274(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2896C>A |
| AA Mutation | p.Gln966Lys(p.Q966K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000324134 |
| Start | 53798265:53798265(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs754537076 |
| CDS Mutation | c.2905G>A |
| AA Mutation | p.Ala969Thr(p.A969T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000324134 |
| Start | 53824150:53824150(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs762604819 |
| CDS Mutation | c.25G>A |
| AA Mutation | p.Gly9Ser(p.G9S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000324134 |
| Start | 53809734:53809734(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1925C>T |
| AA Mutation | p.Ala642Val(p.A642V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000324134 |
| Start | 53811238:53811238(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.421G>A |
| AA Mutation | p.Glu141Lys(p.E141K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000324134 |
| Start | 53803958:53803958(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2579C>T |
| AA Mutation | p.Thr860Ile(p.T860I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000324134 |
| Start | 53796018:53796018(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2939G>T |
| AA Mutation | p.Cys980Phe(p.C980F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000324134 |
| Start | 53796012:53796012(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2945T>C |
| AA Mutation | p.Leu982Pro(p.L982P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000324134 |
| Start | 53810604:53810604(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1055G>A |
| AA Mutation | p.Arg352His(p.R352H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000324134 |
| Start | 53809719:53809719(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1940A>G |
| AA Mutation | p.His647Arg(p.H647R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000324134 |
| Start | 53811006:53811006(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs749659859 |
| CDS Mutation | c.653C>T |
| AA Mutation | p.Ala218Val(p.A218V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000324134 |
| Start | 53805398:53805398(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2296C>G |
| AA Mutation | p.Leu766Val(p.L766V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000324134 |
| Start | 53801297:53801297(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2686C>A |
| AA Mutation | p.Leu896Met(p.L896M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000324134 |
| Start | 53824078:53824078(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.97G>T |
| AA Mutation | p.Gly33Trp(p.G33W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000324134 |
| Start | 53810851:53810851(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.808A>G |
| AA Mutation | p.Ser270Gly(p.S270G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000324134 |
| Start | 53811222:53811222(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.437G>A |
| AA Mutation | p.Arg146His(p.R146H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000324134 |
| Start | 53794088:53794088(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs148506660 |
| CDS Mutation | c.3147G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000324134 |
| Start | 53811005:53811005(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs745766441 |
| CDS Mutation | c.654G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000324134 |
| Start | 53810318:53810318(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs577056280 |
| CDS Mutation | c.1341G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000324134 |
| Start | 53810777:53810777(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs147080557 |
| CDS Mutation | c.882C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000324134 |
| Start | 53801304:53801304(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs542637537 |
| CDS Mutation | c.2679G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000324134 |
| Start | 53798284:53798284(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2886T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000324134 |
| Start | 53810477:53810477(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1182C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 25 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000324134 |
| Start | 53807550:53807550(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs777281641 |
| CDS Mutation | c.2188delG |
| AA Mutation | p.Val730Ter(p.V730*) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 26 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000324134 |
| Start | 53794084:53794084(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs199475871 |
| CDS Mutation | c.3151C>T |
| AA Mutation | p.Arg1051Ter(p.R1051*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |