Primary Site >> Stomach Cancer
Gene >> LRRN1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000319331 |
| Start | 3845719:3845719(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1078C>T |
| AA Mutation | p.Leu360Phe(p.L360F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000319331 |
| Start | 3845630:3845630(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs367980574 |
| CDS Mutation | c.989G>A |
| AA Mutation | p.Arg330His(p.R330H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000319331 |
| Start | 3845727:3845727(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1086T>A |
| AA Mutation | p.Asn362Lys(p.N362K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000319331 |
| Start | 3844679:3844679(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.38T>C |
| AA Mutation | p.Leu13Ser(p.L13S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000319331 |
| Start | 3844825:3844825(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.184C>T |
| AA Mutation | p.Arg62Cys(p.R62C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000319331 |
| Start | 3846349:3846349(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1708T>C |
| AA Mutation | p.Tyr570His(p.Y570H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000319331 |
| Start | 3846507:3846507(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1866C>A |
| AA Mutation | p.Asp622Glu(p.D622E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000319331 |
| Start | 3844888:3844888(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.247A>G |
| AA Mutation | p.Asn83Asp(p.N83D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000319331 |
| Start | 3845418:3845418(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.777G>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000319331 |
| Start | 3844876:3844876(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.235T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000319331 |
| Start | 3846492:3846492(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1851C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000319331 |
| Start | 3846636:3846636(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.2000delA |
| AA Mutation | p.Lys667SerfsTer11(p.K667Sfs*11) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000319331 |
| Start | 3845641:3845641(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs370982701 |
| CDS Mutation | c.1000C>T |
| AA Mutation | p.Arg334Ter(p.R334*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |