Primary Site >> Stomach Cancer
Gene >> SDHA
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264932 |
| Start | 240451:240451(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs397514541 |
| CDS Mutation | c.1526C>T |
| AA Mutation | p.Ser509Leu(p.S509L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264932 |
| Start | 233554:233554(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.973A>G |
| AA Mutation | p.Arg325Gly(p.R325G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264932 |
| Start | 230955:230955(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.850G>T |
| AA Mutation | p.Gly284Cys(p.G284C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264932 |
| Start | 235295:235295(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1216G>A |
| AA Mutation | p.Val406Met(p.V406M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264932 |
| Start | 230886:230886(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs143484394 |
| CDS Mutation | c.781C>T |
| AA Mutation | p.Arg261Cys(p.R261C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264932 |
| Start | 218371:218371(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.16G>A |
| AA Mutation | p.Gly6Ser(p.G6S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264932 |
| Start | 256376:256376(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs375396913 |
| CDS Mutation | c.1951G>A |
| AA Mutation | p.Glu651Lys(p.E651K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264932 |
| Start | 230883:230883(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.778G>A |
| AA Mutation | p.Gly260Arg(p.G260R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264932 |
| Start | 251100:251100(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs9809219 |
| CDS Mutation | c.1660C>T |
| AA Mutation | p.Arg554Trp(p.R554W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264932 |
| Start | 225941:225941(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.515C>T |
| AA Mutation | p.Ala172Val(p.A172V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000264932 |
| Start | 230882:230882(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs140243793 |
| CDS Mutation | c.777C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000264932 |
| Start | 233595:233595(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201341132 |
| CDS Mutation | c.1014G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000264932 |
| Start | 240386:240386(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs187540602 |
| CDS Mutation | c.1461C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000264932 |
| Start | 235147:235147(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1068C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000264932 |
| Start | 235168:235168(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs368488126 |
| CDS Mutation | c.1089C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |