Primary Site >> Stomach Cancer
Gene >> PSD
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000020673 |
| Start | 102404670:102404670(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2613C>A |
| AA Mutation | p.Phe871Leu(p.F871L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000020673 |
| Start | 102416959:102416959(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.80C>T |
| AA Mutation | p.Pro27Leu(p.P27L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000020673 |
| Start | 102404695:102404695(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs368237669 |
| CDS Mutation | c.2588G>A |
| AA Mutation | p.Arg863His(p.R863H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000020673 |
| Start | 102415004:102415004(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.983C>T |
| AA Mutation | p.Ala328Val(p.A328V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000020673 |
| Start | 102414048:102414048(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs751241410 |
| CDS Mutation | c.1274C>T |
| AA Mutation | p.Ser425Leu(p.S425L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000020673 |
| Start | 102410911:102410911(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs765649110 |
| CDS Mutation | c.2038G>A |
| AA Mutation | p.Gly680Arg(p.G680R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000020673 |
| Start | 102415029:102415029(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs774151281 |
| CDS Mutation | c.958A>G |
| AA Mutation | p.Ser320Gly(p.S320G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000020673 |
| Start | 102413868:102413868(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1454A>G |
| AA Mutation | p.Glu485Gly(p.E485G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000020673 |
| Start | 102416897:102416897(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs761558318 |
| CDS Mutation | c.142C>T |
| AA Mutation | p.Arg48Trp(p.R48W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000020673 |
| Start | 102416971:102416971(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs749171096 |
| CDS Mutation | c.68G>A |
| AA Mutation | p.Arg23His(p.R23H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000020673 |
| Start | 102417003:102417003(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs747969446 |
| CDS Mutation | c.36C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000020673 |
| Start | 102411714:102411714(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1935C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000020673 |
| Start | 102414167:102414167(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1155T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000020673 |
| Start | 102414191:102414191(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1131G>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000020673 |
| Start | 102416446:102416446(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.593delG |
| AA Mutation | p.Gly198AlafsTer19(p.G198Afs*19) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000020673 |
| Start | 102415202:102415202(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.785delC |
| AA Mutation | p.Pro262HisfsTer32(p.P262Hfs*32) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000020673 |
| Start | 102416024:102416024(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs774150367 |
| CDS Mutation | c.750delC |
| AA Mutation | p.Ser251AlafsTer43(p.S251Afs*43) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000020673 |
| Start | 102415201:102415202(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | rs768369085 |
| CDS Mutation | c.785dupC |
| AA Mutation | p.Ser263IlefsTer38(p.S263Ifs*38) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |