Primary Site >> Stomach Cancer
Gene >> PADI2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000375486 |
| Start | 17069066:17069066(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1976A>C |
| AA Mutation | p.Lys659Thr(p.K659T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000375486 |
| Start | 17104880:17104880(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.274A>C |
| AA Mutation | p.Lys92Gln(p.K92Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000375486 |
| Start | 17104993:17104993(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs367699636 |
| CDS Mutation | c.161G>A |
| AA Mutation | p.Arg54His(p.R54H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000375486 |
| Start | 17104922:17104922(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs187842443 |
| CDS Mutation | c.232C>T |
| AA Mutation | p.Arg78Trp(p.R78W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000375486 |
| Start | 17083818:17083818(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.958T>A |
| AA Mutation | p.Phe320Ile(p.F320I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000375486 |
| Start | 17093597:17093597(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.499T>G |
| AA Mutation | p.Cys167Gly(p.C167G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000375486 |
| Start | 17075804:17075804(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1330A>G |
| AA Mutation | p.Thr444Ala(p.T444A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000375486 |
| Start | 17092414:17092414(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs768592470 |
| CDS Mutation | c.649G>A |
| AA Mutation | p.Val217Met(p.V217M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000375486 |
| Start | 17074921:17074921(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs746982569 |
| CDS Mutation | c.1484C>T |
| AA Mutation | p.Ser495Leu(p.S495L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000375486 |
| Start | 17105059:17105059(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs148878349 |
| CDS Mutation | c.95C>T |
| AA Mutation | p.Ala32Val(p.A32V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000375486 |
| Start | 17092503:17092503(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs372515836 |
| CDS Mutation | c.560G>A |
| AA Mutation | p.Arg187Gln(p.R187Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000375486 |
| Start | 17069168:17069168(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1874T>A |
| AA Mutation | p.Leu625Gln(p.L625Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000375486 |
| Start | 17086681:17086681(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs138756249 |
| CDS Mutation | c.674G>A |
| AA Mutation | p.Arg225His(p.R225H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000375486 |
| Start | 17105058:17105058(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs772447537 |
| CDS Mutation | c.96G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000375486 |
| Start | 17084619:17084619(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs771499888 |
| CDS Mutation | c.918C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000375486 |
| Start | 17075753:17075753(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1381G>T |
| AA Mutation | p.Glu461Ter(p.E461*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000375486 |
| Start | 17083746:17083746(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs777550918 |
| CDS Mutation | c.1030C>T |
| AA Mutation | p.Arg344Ter(p.R344*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |