Primary Site >> Stomach Cancer
Gene >> WWP1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265428 |
| Start | 86411651:86411651(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.838G>T |
| AA Mutation | p.Asp280Tyr(p.D280Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000265428 |
| Start | 86442776:86442776(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1996A>G |
| AA Mutation | p.Met666Val(p.M666V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265428 |
| Start | 86461269:86461269(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2545T>C |
| AA Mutation | p.Phe849Leu(p.F849L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265428 |
| Start | 86380807:86380807(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs767773883 |
| CDS Mutation | c.152C>T |
| AA Mutation | p.Thr51Met(p.T51M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265428 |
| Start | 86380818:86380818(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.163A>C |
| AA Mutation | p.Lys55Gln(p.K55Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265428 |
| Start | 86411792:86411792(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.979G>A |
| AA Mutation | p.Ala327Thr(p.A327T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265428 |
| Start | 86438591:86438591(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1756G>A |
| AA Mutation | p.Ala586Thr(p.A586T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265428 |
| Start | 86461843:86461843(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2666C>T |
| AA Mutation | p.Thr889Ile(p.T889I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265428 |
| Start | 86442655:86442655(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1875C>A |
| AA Mutation | p.Asn625Lys(p.N625K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265428 |
| Start | 86457994:86457994(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2468G>A |
| AA Mutation | p.Arg823Lys(p.R823K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265428 |
| Start | 86411870:86411870(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1057T>G |
| AA Mutation | p.Ser353Ala(p.S353A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265428 |
| Start | 86461272:86461272(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2548G>C |
| AA Mutation | p.Val850Leu(p.V850L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265428 |
| Start | 86381552:86381552(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs371650373 |
| CDS Mutation | c.257G>A |
| AA Mutation | p.Arg86His(p.R86H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000265428 |
| Start | 86452625:86452625(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2340T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000265428 |
| Start | 86442703:86442703(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1923G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000265428 |
| Start | 86398615:86398615(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs750015761 |
| CDS Mutation | c.516G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000265428 |
| Start | 86411782:86411782(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.969T>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000265428 |
| Start | 86427737:86427737(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs771835365 |
| CDS Mutation | c.1252C>T |
| AA Mutation | p.Arg418Ter(p.R418*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |