Primary Site >> Stomach Cancer
Gene >> POLR2A
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000617998 |
| Start | 7495957:7495957(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.110C>T |
| AA Mutation | p.Thr37Met(p.T37M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000617998 |
| Start | 7496305:7496305(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.322C>T |
| AA Mutation | p.Arg108Cys(p.R108C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000617998 |
| Start | 7513072:7513072(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4808G>A |
| AA Mutation | p.Arg1603His(p.R1603H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000617998 |
| Start | 7502571:7502571(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2626G>A |
| AA Mutation | p.Asp876Asn(p.D876N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000617998 |
| Start | 7513579:7513579(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.5315C>T |
| AA Mutation | p.Thr1772Ile(p.T1772I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000617998 |
| Start | 7511237:7511237(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3836T>C |
| AA Mutation | p.Met1279Thr(p.M1279T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000617998 |
| Start | 7512198:7512198(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4346A>G |
| AA Mutation | p.Asp1449Gly(p.D1449G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000617998 |
| Start | 7513689:7513689(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.5425C>T |
| AA Mutation | p.Pro1809Ser(p.P1809S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000617998 |
| Start | 7503409:7503409(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs548638112 |
| CDS Mutation | c.2953C>T |
| AA Mutation | p.Arg985Trp(p.R985W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000617998 |
| Start | 7496521:7496521(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.445A>G |
| AA Mutation | p.Lys149Glu(p.K149E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000617998 |
| Start | 7499126:7499126(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs775983104 |
| CDS Mutation | c.1423C>T |
| AA Mutation | p.Arg475Cys(p.R475C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000617998 |
| Start | 7501622:7501622(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2242G>A |
| AA Mutation | p.Ala748Thr(p.A748T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000617998 |
| Start | 7509122:7509122(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3644A>C |
| AA Mutation | p.Glu1215Ala(p.E1215A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000617998 |
| Start | 7511500:7511500(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4013C>T |
| AA Mutation | p.Thr1338Met(p.T1338M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000617998 |
| Start | 7503264:7503264(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2900G>T |
| AA Mutation | p.Arg967Met(p.R967M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000617998 |
| Start | 7498121:7498121(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs763272826 |
| CDS Mutation | c.1246G>A |
| AA Mutation | p.Ala416Thr(p.A416T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000617998 |
| Start | 7500660:7500660(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1693A>G |
| AA Mutation | p.Met565Val(p.M565V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000617998 |
| Start | 7513490:7513490(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.5226A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000617998 |
| Start | 7499065:7499065(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1362C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000617998 |
| Start | 7513751:7513751(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs370656689 |
| CDS Mutation | c.5487G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000617998 |
| Start | 7513886:7513886(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.5622T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000617998 |
| Start | 7503665:7503665(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs771846320 |
| CDS Mutation | c.3114G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000617998 |
| Start | 7496880:7496880(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.654A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000617998 |
| Start | 7513785:7513785(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.5524delC |
| AA Mutation | p.Gln1842AsnfsTer72(p.Q1842Nfs*72) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 25 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000617998 |
| Start | 7496527:7496527(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.455delA |
| AA Mutation | p.Asn152ThrfsTer24(p.N152Tfs*24) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 26 |
| Mutation Consequence | splice_donor_variant |
| Transcription ID | ENST00000617998 |
| Start | 7496347:7496347(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.363+1G>A |
| Mutation Classification | Splice_Site |
| Feature Type | Transcript |