Primary Site >> Stomach Cancer
Gene >> CCNF
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000397066 |
| Start | 2456910:2456910(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs142532028 |
| CDS Mutation | c.2251C>T |
| AA Mutation | p.Arg751Cys(p.R751C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000397066 |
| Start | 2431196:2431196(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs560665712 |
| CDS Mutation | c.83G>A |
| AA Mutation | p.Arg28Gln(p.R28Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000397066 |
| Start | 2453464:2453464(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1642G>A |
| AA Mutation | p.Asp548Asn(p.D548N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000397066 |
| Start | 2437242:2437242(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs764445847 |
| CDS Mutation | c.460C>T |
| AA Mutation | p.Arg154Cys(p.R154C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000397066 |
| Start | 2439816:2439816(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.767G>T |
| AA Mutation | p.Trp256Leu(p.W256L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000397066 |
| Start | 2437152:2437152(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs773326682 |
| CDS Mutation | c.370G>A |
| AA Mutation | p.Ala124Thr(p.A124T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000397066 |
| Start | 2431175:2431175(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200973445 |
| CDS Mutation | c.62G>A |
| AA Mutation | p.Arg21Gln(p.R21Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000397066 |
| Start | 2456772:2456772(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs142923904 |
| CDS Mutation | c.2113G>A |
| AA Mutation | p.Val705Ile(p.V705I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000397066 |
| Start | 2455426:2455426(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1747G>T |
| AA Mutation | p.Gly583Cys(p.G583C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000397066 |
| Start | 2437280:2437280(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs150541774 |
| CDS Mutation | c.498C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000397066 |
| Start | 2432984:2432984(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.195G>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000397066 |
| Start | 2439442:2439442(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.684C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000397066 |
| Start | 2449404:2449404(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs777340745 |
| CDS Mutation | c.1341C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000397066 |
| Start | 2453499:2453499(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs555465125 |
| CDS Mutation | c.1677C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000397066 |
| Start | 2445530:2445530(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs545944447 |
| CDS Mutation | c.1002C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000397066 |
| Start | 2453466:2453466(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1649delC |
| AA Mutation | p.Pro550ArgfsTer80(p.P550Rfs*80) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |