Primary Site >> Stomach Cancer
Gene >> CLDN9
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000445369 |
| Start | 3013741:3013741(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.379C>T |
| AA Mutation | p.Leu127Phe(p.L127F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000445369 |
| Start | 3013921:3013921(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.559C>A |
| AA Mutation | p.Pro187Thr(p.P187T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000445369 |
| Start | 3013691:3013691(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.329A>G |
| AA Mutation | p.Asp110Gly(p.D110G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000445369 |
| Start | 3013437:3013437(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs368045321 |
| CDS Mutation | c.75C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000445369 |
| Start | 3013539:3013539(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs372231955 |
| CDS Mutation | c.177G>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000445369 |
| Start | 3013872:3013872(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.510G>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000445369 |
| Start | 3013533:3013533(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs747585456 |
| CDS Mutation | c.171G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000445369 |
| Start | 3013441:3013441(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.79C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000445369 |
| Start | 3013713:3013713(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs746690844 |
| CDS Mutation | c.351C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000445369 |
| Start | 3013894:3013894(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.537delG |
| AA Mutation | p.Leu180SerfsTer196(p.L180Sfs*196) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000445369 |
| Start | 3013809:3013809(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs771833909 |
| CDS Mutation | c.451delC |
| AA Mutation | p.Leu151TrpfsTer225(p.L151Wfs*225) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000445369 |
| Start | 3013916:3013917(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | rs753671764 |
| CDS Mutation | c.560dupC |
| AA Mutation | p.Pro188AlafsTer96(p.P188Afs*96) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |