Primary Site >> Stomach Cancer
Gene >> FOXRED1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263578 |
| Start | 126277645:126277645(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs766922221 |
| CDS Mutation | c.1417C>T |
| AA Mutation | p.Arg473Cys(p.R473C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263578 |
| Start | 126276441:126276441(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs772550290 |
| CDS Mutation | c.1019C>T |
| AA Mutation | p.Pro340Leu(p.P340L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263578 |
| Start | 126272978:126272978(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.316G>A |
| AA Mutation | p.Ala106Thr(p.A106T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263578 |
| Start | 126277514:126277514(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1286T>C |
| AA Mutation | p.Val429Ala(p.V429A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263578 |
| Start | 126271450:126271450(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.99G>T |
| AA Mutation | p.Lys33Asn(p.K33N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263578 |
| Start | 126271548:126271548(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.197T>C |
| AA Mutation | p.Val66Ala(p.V66A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263578 |
| Start | 126276189:126276189(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.941G>A |
| AA Mutation | p.Gly314Asp(p.G314D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263578 |
| Start | 126276201:126276201(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.953C>A |
| AA Mutation | p.Pro318His(p.P318H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263578 |
| Start | 126275013:126275013(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs745954163 |
| CDS Mutation | c.623C>T |
| AA Mutation | p.Ala208Val(p.A208V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000263578 |
| Start | 126277082:126277082(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs759206750 |
| CDS Mutation | c.1113G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000263578 |
| Start | 126277576:126277576(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs755778634 |
| CDS Mutation | c.1348C>T |
| AA Mutation | p.Arg450Ter(p.R450*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |