Primary Site >> Stomach Cancer
Gene >> NLRX1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000292199 |
| Start | 119173905:119173905(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs146004436 |
| CDS Mutation | c.656G>A |
| AA Mutation | p.Arg219His(p.R219H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000292199 |
| Start | 119182327:119182327(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2588C>A |
| AA Mutation | p.Pro863His(p.P863H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000292199 |
| Start | 119182236:119182236(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2497C>A |
| AA Mutation | p.Arg833Ser(p.R833S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000292199 |
| Start | 119179882:119179882(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1861G>A |
| AA Mutation | p.Glu621Lys(p.E621K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000292199 |
| Start | 119175012:119175012(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1409G>A |
| AA Mutation | p.Arg470His(p.R470H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000292199 |
| Start | 119175047:119175047(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1444G>A |
| AA Mutation | p.Val482Met(p.V482M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000292199 |
| Start | 119182108:119182108(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs569295450 |
| CDS Mutation | c.2369C>T |
| AA Mutation | p.Pro790Leu(p.P790L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000292199 |
| Start | 119173778:119173778(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.529C>T |
| AA Mutation | p.Arg177Cys(p.R177C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000292199 |
| Start | 119182149:119182149(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2410G>A |
| AA Mutation | p.Ala804Thr(p.A804T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000292199 |
| Start | 119173898:119173898(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.649G>A |
| AA Mutation | p.Ala217Thr(p.A217T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000292199 |
| Start | 119174492:119174492(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs774043342 |
| CDS Mutation | c.889C>T |
| AA Mutation | p.Arg297Cys(p.R297C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000292199 |
| Start | 119179934:119179934(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1913T>C |
| AA Mutation | p.Val638Ala(p.V638A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000292199 |
| Start | 119182131:119182131(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs751553782 |
| CDS Mutation | c.2392G>A |
| AA Mutation | p.Val798Met(p.V798M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000292199 |
| Start | 119173897:119173897(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.648G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000292199 |
| Start | 119174620:119174620(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1017T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000292199 |
| Start | 119180031:119180031(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2010G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000292199 |
| Start | 119174026:119174026(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.777T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000292199 |
| Start | 119174767:119174767(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200299072 |
| CDS Mutation | c.1164G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000292199 |
| Start | 119183169:119183169(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.2663delG |
| AA Mutation | p.Gly888ValfsTer13(p.G888Vfs*13) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000292199 |
| Start | 119173672:119173672(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs767102699 |
| CDS Mutation | c.428delC |
| AA Mutation | p.Pro143HisfsTer81(p.P143Hfs*81) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |