Primary Site >> Stomach Cancer
Gene >> TMEM41A
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000421852 |
| Start | 185491652:185491652(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.680C>T |
| AA Mutation | p.Ala227Val(p.A227V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000421852 |
| Start | 185494761:185494761(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.436G>A |
| AA Mutation | p.Val146Met(p.V146M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000421852 |
| Start | 185496920:185496920(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.181T>C |
| AA Mutation | p.Tyr61His(p.Y61H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000421852 |
| Start | 185495277:185495277(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.312G>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000421852 |
| Start | 185496978:185496978(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.123G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000421852 |
| Start | 185494730:185494730(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs758476632 |
| CDS Mutation | c.467delT |
| AA Mutation | p.Phe156SerfsTer5(p.F156Sfs*5) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000421852 |
| Start | 185494729:185494730(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | rs766594251 |
| CDS Mutation | c.467dupT |
| AA Mutation | p.Leu158IlefsTer40(p.L158Ifs*40) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |