Primary Site >> Stomach Cancer
Gene >> LIMA1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000341247 |
| Start | 50222232:50222232(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.419G>A |
| AA Mutation | p.Gly140Asp(p.G140D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000341247 |
| Start | 50192474:50192474(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1118G>A |
| AA Mutation | p.Ser373Asn(p.S373N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000341247 |
| Start | 50222317:50222317(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs146061384 |
| CDS Mutation | c.334G>A |
| AA Mutation | p.Ala112Thr(p.A112T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000341247 |
| Start | 50222357:50222357(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.294G>T |
| AA Mutation | p.Arg98Ser(p.R98S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000341247 |
| Start | 50177244:50177244(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2100A>T |
| AA Mutation | p.Gln700His(p.Q700H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000341247 |
| Start | 50204669:50204669(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.747G>T |
| AA Mutation | p.Glu249Asp(p.E249D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000341247 |
| Start | 50177522:50177522(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1822G>A |
| AA Mutation | p.Val608Met(p.V608M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000341247 |
| Start | 50182008:50182008(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs760289112 |
| CDS Mutation | c.1170C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |