Primary Site >> Stomach Cancer
Gene >> FRMD1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000283309 |
| Start | 168066777:168066777(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs151107075 |
| CDS Mutation | c.439G>A |
| AA Mutation | p.Val147Met(p.V147M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000283309 |
| Start | 168057129:168057129(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs771877804 |
| CDS Mutation | c.1618G>A |
| AA Mutation | p.Gly540Arg(p.G540R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000283309 |
| Start | 168064993:168064993(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs372120473 |
| CDS Mutation | c.526G>A |
| AA Mutation | p.Ala176Thr(p.A176T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000283309 |
| Start | 168061876:168061876(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs186693438 |
| CDS Mutation | c.976G>A |
| AA Mutation | p.Ala326Thr(p.A326T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000283309 |
| Start | 168078907:168078907(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs767006393 |
| CDS Mutation | c.188G>A |
| AA Mutation | p.Arg63Gln(p.R63Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000283309 |
| Start | 168061043:168061043(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs533290722 |
| CDS Mutation | c.1060C>T |
| AA Mutation | p.Arg354Trp(p.R354W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000283309 |
| Start | 168064994:168064994(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs376956774 |
| CDS Mutation | c.525C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000283309 |
| Start | 168060782:168060783(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.1320dupC |
| AA Mutation | p.Ser441GlnfsTer5(p.S441Qfs*5) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |