Primary Site >> Stomach Cancer
Gene >> NOS2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000313735 |
| Start | 27782990:27782990(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200238137 |
| CDS Mutation | c.584G>A |
| AA Mutation | p.Arg195His(p.R195H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000313735 |
| Start | 27781173:27781173(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.727G>A |
| AA Mutation | p.Ala243Thr(p.A243T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000313735 |
| Start | 27770945:27770945(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1777T>C |
| AA Mutation | p.Phe593Leu(p.F593L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000313735 |
| Start | 27769002:27769002(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2009G>A |
| AA Mutation | p.Arg670His(p.R670H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000313735 |
| Start | 27757301:27757301(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200632738 |
| CDS Mutation | c.3407C>T |
| AA Mutation | p.Ala1136Val(p.A1136V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000313735 |
| Start | 27770972:27770972(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201443307 |
| CDS Mutation | c.1750C>T |
| AA Mutation | p.Arg584Trp(p.R584W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000313735 |
| Start | 27780777:27780777(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.994G>A |
| AA Mutation | p.Glu332Lys(p.E332K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000313735 |
| Start | 27780849:27780849(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.922G>A |
| AA Mutation | p.Val308Ile(p.V308I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000313735 |
| Start | 27778760:27778760(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1211A>G |
| AA Mutation | p.His404Arg(p.H404R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000313735 |
| Start | 27774438:27774438(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1295C>T |
| AA Mutation | p.Thr432Ile(p.T432I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000313735 |
| Start | 27778756:27778756(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1215G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000313735 |
| Start | 27778981:27778981(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs140983392 |
| CDS Mutation | c.1080C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000313735 |
| Start | 27789616:27789616(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.183G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000313735 |
| Start | 27778957:27778957(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1104C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000313735 |
| Start | 27780865:27780865(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs753280840 |
| CDS Mutation | c.906C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000313735 |
| Start | 27781147:27781147(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.753T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000313735 |
| Start | 27780814:27780814(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs34719207 |
| CDS Mutation | c.957C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |