Primary Site >> Stomach Cancer
Gene >> NLRP5
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000390649 |
| Start | 56004080:56004080(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201123213 |
| CDS Mutation | c.427C>T |
| AA Mutation | p.Arg143Trp(p.R143W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000390649 |
| Start | 56027600:56027600(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200829045 |
| CDS Mutation | c.1367G>A |
| AA Mutation | p.Arg456His(p.R456H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000390649 |
| Start | 56003878:56003878(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.225A>C |
| AA Mutation | p.Glu75Asp(p.E75D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000390649 |
| Start | 56053660:56053660(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs374153940 |
| CDS Mutation | c.3151G>A |
| AA Mutation | p.Ala1051Thr(p.A1051T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000390649 |
| Start | 56032614:56032614(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2280G>A |
| AA Mutation | p.Met760Ile(p.M760I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000390649 |
| Start | 56028442:56028442(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs537471101 |
| CDS Mutation | c.2209C>T |
| AA Mutation | p.Arg737Trp(p.R737W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000390649 |
| Start | 56008815:56008815(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.470C>T |
| AA Mutation | p.Thr157Met(p.T157M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000390649 |
| Start | 56053760:56053760(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs572932270 |
| CDS Mutation | c.3251C>T |
| AA Mutation | p.Ala1084Val(p.A1084V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000390649 |
| Start | 56053694:56053694(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs761657995 |
| CDS Mutation | c.3185C>T |
| AA Mutation | p.Ser1062Leu(p.S1062L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000390649 |
| Start | 56027081:56027081(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.848T>A |
| AA Mutation | p.Val283Asp(p.V283D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000390649 |
| Start | 56027411:56027411(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1178G>C |
| AA Mutation | p.Ser393Thr(p.S393T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000390649 |
| Start | 56050492:56050492(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs77601682 |
| CDS Mutation | c.3032C>T |
| AA Mutation | p.Thr1011Met(p.T1011M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000390649 |
| Start | 56027616:56027616(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1383C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000390649 |
| Start | 56003935:56003935(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.282C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000390649 |
| Start | 56027496:56027496(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1263C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000390649 |
| Start | 56038172:56038172(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2763C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000390649 |
| Start | 56027604:56027604(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs370683647 |
| CDS Mutation | c.1371G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |