Primary Site >> Stomach Cancer
Gene >> DNER
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000341772 |
| Start | 229591650:229591650(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs143332732 |
| CDS Mutation | c.515C>T |
| AA Mutation | p.Thr172Met(p.T172M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000341772 |
| Start | 229418216:229418216(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1501T>C |
| AA Mutation | p.Tyr501His(p.Y501H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000341772 |
| Start | 229512897:229512897(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1033A>T |
| AA Mutation | p.Thr345Ser(p.T345S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000341772 |
| Start | 229366987:229366987(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1988G>A |
| AA Mutation | p.Arg663His(p.R663H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000341772 |
| Start | 229366898:229366898(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2077G>T |
| AA Mutation | p.Ala693Ser(p.A693S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000341772 |
| Start | 229366965:229366965(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2010G>T |
| AA Mutation | p.Gln670His(p.Q670H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000341772 |
| Start | 229418146:229418146(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1571T>A |
| AA Mutation | p.Val524Asp(p.V524D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000341772 |
| Start | 229591792:229591792(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.373G>C |
| AA Mutation | p.Glu125Gln(p.E125Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000341772 |
| Start | 229512830:229512830(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1100C>A |
| AA Mutation | p.Ala367Glu(p.A367E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000341772 |
| Start | 229447476:229447476(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201881122 |
| CDS Mutation | c.1326C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000341772 |
| Start | 229447500:229447500(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs140576705 |
| CDS Mutation | c.1302C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000341772 |
| Start | 229366884:229366884(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs775072382 |
| CDS Mutation | c.2091C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000341772 |
| Start | 229418148:229418148(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1569C>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000341772 |
| Start | 229358606:229358606(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs139616890 |
| CDS Mutation | c.2148C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |