Primary Site >> Stomach Cancer
Gene >> FGA
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000302053 |
| Start | 154587562:154587562(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.460C>A |
| AA Mutation | p.Leu154Ile(p.L154I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000302053 |
| Start | 154585576:154585576(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1853G>A |
| AA Mutation | p.Ser618Asn(p.S618N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000302053 |
| Start | 154584772:154584772(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1953G>T |
| AA Mutation | p.Lys651Asn(p.K651N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000302053 |
| Start | 154586480:154586480(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.949G>T |
| AA Mutation | p.Gly317Trp(p.G317W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000302053 |
| Start | 154584440:154584440(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs150073296 |
| CDS Mutation | c.2285C>T |
| AA Mutation | p.Ala762Val(p.A762V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000302053 |
| Start | 154585950:154585950(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1479G>T |
| AA Mutation | p.Glu493Asp(p.E493D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000302053 |
| Start | 154588825:154588825(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.332A>G |
| AA Mutation | p.Glu111Gly(p.E111G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000302053 |
| Start | 154589514:154589514(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs121909606 |
| CDS Mutation | c.103C>T |
| AA Mutation | p.Arg35Cys(p.R35C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000302053 |
| Start | 154584165:154584165(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs747707945 |
| CDS Mutation | c.2560A>G |
| AA Mutation | p.Arg854Gly(p.R854G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000302053 |
| Start | 154589517:154589517(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs746367635 |
| CDS Mutation | c.100G>A |
| AA Mutation | p.Val34Met(p.V34M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000302053 |
| Start | 154586665:154586665(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.764C>T |
| AA Mutation | p.Pro255Leu(p.P255L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000302053 |
| Start | 154586892:154586892(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.537T>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000302053 |
| Start | 154586664:154586664(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs779582722 |
| CDS Mutation | c.765G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000302053 |
| Start | 154585935:154585935(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs768620557 |
| CDS Mutation | c.1494C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000302053 |
| Start | 154585974:154585974(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs774171561 |
| CDS Mutation | c.1455C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000302053 |
| Start | 154586507:154586507(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs776817952 |
| CDS Mutation | c.922C>T |
| AA Mutation | p.Arg308Ter(p.R308*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |