Primary Site >> Stomach Cancer
Gene >> CNDP2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000324262 |
| Start | 74505866:74505866(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.222G>C |
| AA Mutation | p.Glu74Asp(p.E74D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000324262 |
| Start | 74510849:74510849(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.493A>G |
| AA Mutation | p.Met165Val(p.M165V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000324262 |
| Start | 74513621:74513621(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs540790918 |
| CDS Mutation | c.805G>A |
| AA Mutation | p.Val269Ile(p.V269I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000324262 |
| Start | 74505982:74505982(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.338G>A |
| AA Mutation | p.Ser113Asn(p.S113N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000324262 |
| Start | 74501371:74501371(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.103C>T |
| AA Mutation | p.Pro35Ser(p.P35S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000324262 |
| Start | 74518989:74518989(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1251T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000324262 |
| Start | 74518570:74518570(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200121262 |
| CDS Mutation | c.1140C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000324262 |
| Start | 74501433:74501433(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.170delG |
| AA Mutation | p.Gly57AlafsTer85(p.G57Afs*85) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000324262 |
| Start | 74506005:74506005(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.361C>T |
| AA Mutation | p.Arg121Ter(p.R121*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |