Primary Site >> Stomach Cancer
Gene >> TNRC6C
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000301624 |
| Start | 78103529:78103529(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4688C>T |
| AA Mutation | p.Ala1563Val(p.A1563V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000301624 |
| Start | 78083157:78083157(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3468G>T |
| AA Mutation | p.Gln1156His(p.Q1156H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000301624 |
| Start | 78049630:78049630(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs771723841 |
| CDS Mutation | c.568A>G |
| AA Mutation | p.Met190Val(p.M190V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000301624 |
| Start | 78050107:78050107(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1045C>G |
| AA Mutation | p.Gln349Glu(p.Q349E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000301624 |
| Start | 78049264:78049264(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.202A>G |
| AA Mutation | p.Ser68Gly(p.S68G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000301624 |
| Start | 78093068:78093068(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs781193694 |
| CDS Mutation | c.4106G>A |
| AA Mutation | p.Arg1369His(p.R1369H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000301624 |
| Start | 78050681:78050681(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1619C>T |
| AA Mutation | p.Ser540Leu(p.S540L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000301624 |
| Start | 78091480:78091480(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3843G>T |
| AA Mutation | p.Met1281Ile(p.M1281I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000301624 |
| Start | 78050790:78050790(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1728G>T |
| AA Mutation | p.Lys576Asn(p.K576N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000301624 |
| Start | 78075187:78075187(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2969C>T |
| AA Mutation | p.Thr990Ile(p.T990I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000301624 |
| Start | 78093106:78093106(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4144A>G |
| AA Mutation | p.Ser1382Gly(p.S1382G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000301624 |
| Start | 78079541:78079541(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3357G>T |
| AA Mutation | p.Gln1119His(p.Q1119H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000301624 |
| Start | 78051030:78051030(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1968G>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000301624 |
| Start | 78049581:78049581(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs148231811 |
| CDS Mutation | c.519C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000301624 |
| Start | 78050019:78050019(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs566474602 |
| CDS Mutation | c.957C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000301624 |
| Start | 78067906:78067906(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.2766delA |
| AA Mutation | p.Gly923AspfsTer6(p.G923Dfs*6) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000301624 |
| Start | 78051025:78051026(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.1969dupG |
| AA Mutation | p.Glu657GlyfsTer13(p.E657Gfs*13) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |