Primary Site >> Stomach Cancer
Gene >> RASA3
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000334062 |
| Start | 114021491:114021491(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.698C>T |
| AA Mutation | p.Ala233Val(p.A233V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000334062 |
| Start | 114015316:114015316(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1298A>G |
| AA Mutation | p.Tyr433Cys(p.Y433C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000334062 |
| Start | 114011229:114011229(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs373938545 |
| CDS Mutation | c.1532C>T |
| AA Mutation | p.Thr511Met(p.T511M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000334062 |
| Start | 114041081:114041081(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.291C>G |
| AA Mutation | p.Ile97Met(p.I97M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000334062 |
| Start | 114016241:114016241(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1237G>A |
| AA Mutation | p.Asp413Asn(p.D413N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000334062 |
| Start | 113992523:113992523(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2207T>G |
| AA Mutation | p.Leu736Arg(p.L736R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000334062 |
| Start | 114021407:114021407(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.782C>T |
| AA Mutation | p.Ala261Val(p.A261V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000334062 |
| Start | 114016260:114016260(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1218C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000334062 |
| Start | 113996710:113996710(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs761708403 |
| CDS Mutation | c.1962G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000334062 |
| Start | 113981752:113981752(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs773788806 |
| CDS Mutation | c.2352C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000334062 |
| Start | 113996557:113996557(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs746078734 |
| CDS Mutation | c.2115G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000334062 |
| Start | 113981784:113981784(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.2320delC |
| AA Mutation | p.Gln774ArgfsTer7(p.Q774Rfs*7) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |