Primary Site >> Stomach Cancer
Gene >> UTP20
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261637 |
| Start | 101342579:101342579(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200766524 |
| CDS Mutation | c.4235C>T |
| AA Mutation | p.Thr1412Met(p.T1412M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261637 |
| Start | 101381147:101381147(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.7592G>T |
| AA Mutation | p.Ser2531Ile(p.S2531I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261637 |
| Start | 101285841:101285841(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs779027623 |
| CDS Mutation | c.286C>G |
| AA Mutation | p.Leu96Val(p.L96V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261637 |
| Start | 101379523:101379523(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.7549G>T |
| AA Mutation | p.Ala2517Ser(p.A2517S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000261637 |
| Start | 101374808:101374808(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs760622502 |
| CDS Mutation | c.7132C>T |
| AA Mutation | p.Arg2378Cys(p.R2378C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261637 |
| Start | 101379476:101379476(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs761229316 |
| CDS Mutation | c.7502A>G |
| AA Mutation | p.Gln2501Arg(p.Q2501R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261637 |
| Start | 101369865:101369865(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.6529T>G |
| AA Mutation | p.Phe2177Val(p.F2177V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261637 |
| Start | 101345576:101345576(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4628C>T |
| AA Mutation | p.Thr1543Ile(p.T1543I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261637 |
| Start | 101345648:101345648(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4700A>G |
| AA Mutation | p.Tyr1567Cys(p.Y1567C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261637 |
| Start | 101342986:101342986(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs768900064 |
| CDS Mutation | c.4342G>A |
| AA Mutation | p.Val1448Ile(p.V1448I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261637 |
| Start | 101383101:101383101(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.7717G>A |
| AA Mutation | p.Asp2573Asn(p.D2573N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261637 |
| Start | 101365510:101365510(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.6010T>G |
| AA Mutation | p.Leu2004Val(p.L2004V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261637 |
| Start | 101373667:101373667(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.7031A>G |
| AA Mutation | p.Lys2344Arg(p.K2344R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261637 |
| Start | 101327095:101327095(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs376327544 |
| CDS Mutation | c.3056G>A |
| AA Mutation | p.Arg1019Gln(p.R1019Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261637 |
| Start | 101327166:101327166(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs771140706 |
| CDS Mutation | c.3127C>T |
| AA Mutation | p.Arg1043Trp(p.R1043W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000261637 |
| Start | 101365608:101365608(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs768499716 |
| CDS Mutation | c.6108G>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000261637 |
| Start | 101373461:101373461(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs199582058 |
| CDS Mutation | c.6939G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000261637 |
| Start | 101329371:101329371(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs144955025 |
| CDS Mutation | c.3339C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000261637 |
| Start | 101356613:101356613(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs577076209 |
| CDS Mutation | c.5454C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000261637 |
| Start | 101299757:101299757(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1506T>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000261637 |
| Start | 101300003:101300003(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1617C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000261637 |
| Start | 101342952:101342952(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs751110666 |
| CDS Mutation | c.4308C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000261637 |
| Start | 101371093:101371093(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.6723C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000261637 |
| Start | 101385998:101385998(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.8239delA |
| AA Mutation | p.Met2747Ter(p.M2747*) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 25 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000261637 |
| Start | 101286379:101286379(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs761528888 |
| CDS Mutation | c.392delT |
| AA Mutation | p.Leu131Ter(p.L131*) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |