Primary Site >> Stomach Cancer
Gene >> RCC1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000373832 |
| Start | 28536376:28536376(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs745611564 |
| CDS Mutation | c.932C>T |
| AA Mutation | p.Ser311Leu(p.S311L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000373832 |
| Start | 28535374:28535374(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.655G>C |
| AA Mutation | p.Gly219Arg(p.G219R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000373832 |
| Start | 28531832:28531832(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.103G>A |
| AA Mutation | p.Gly35Ser(p.G35S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000373832 |
| Start | 28532232:28532232(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs150426843 |
| CDS Mutation | c.323C>T |
| AA Mutation | p.Ser108Leu(p.S108L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000373832 |
| Start | 28535874:28535874(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.665G>A |
| AA Mutation | p.Arg222Gln(p.R222Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000373832 |
| Start | 28531917:28531917(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.188T>C |
| AA Mutation | p.Val63Ala(p.V63A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000373832 |
| Start | 28536805:28536805(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.996T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000373832 |
| Start | 28537965:28537965(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1224C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000373832 |
| Start | 28529881:28529881(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.15C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000373832 |
| Start | 28535986:28535986(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.777C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000373832 |
| Start | 28529897:28529898(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | rs779694464 |
| CDS Mutation | c.38dupC |
| AA Mutation | p.Ala14SerfsTer39(p.A14Sfs*39) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |