Primary Site >> Stomach Cancer
Gene >> MFHAS1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000276282 |
| Start | 8891639:8891639(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1420A>G |
| AA Mutation | p.Ile474Val(p.I474V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000276282 |
| Start | 8892098:8892098(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.961C>T |
| AA Mutation | p.Leu321Phe(p.L321F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000276282 |
| Start | 8891000:8891000(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2059G>A |
| AA Mutation | p.Ala687Thr(p.A687T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000276282 |
| Start | 8891644:8891644(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1415G>A |
| AA Mutation | p.Arg472Gln(p.R472Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000276282 |
| Start | 8890373:8890373(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2686G>A |
| AA Mutation | p.Ala896Thr(p.A896T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000276282 |
| Start | 8890718:8890718(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs370580365 |
| CDS Mutation | c.2341C>T |
| AA Mutation | p.Arg781Trp(p.R781W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000276282 |
| Start | 8892034:8892034(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1025C>T |
| AA Mutation | p.Thr342Ile(p.T342I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000276282 |
| Start | 8890898:8890898(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2161G>A |
| AA Mutation | p.Ala721Thr(p.A721T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000276282 |
| Start | 8890289:8890289(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2770C>G |
| AA Mutation | p.Pro924Ala(p.P924A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000276282 |
| Start | 8892100:8892100(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.959G>A |
| AA Mutation | p.Arg320Gln(p.R320Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000276282 |
| Start | 8891943:8891943(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1116C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000276282 |
| Start | 8797423:8797423(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs769753343 |
| CDS Mutation | c.3067C>T |
| AA Mutation | p.Arg1023Ter(p.R1023*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |