Primary Site >> Stomach Cancer
Gene >> KRT13
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000246635 |
| Start | 41505214:41505214(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.337G>A |
| AA Mutation | p.Asp113Asn(p.D113N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000246635 |
| Start | 41502694:41502694(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1016T>C |
| AA Mutation | p.Leu339Pro(p.L339P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000246635 |
| Start | 41503420:41503420(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs781291691 |
| CDS Mutation | c.602G>A |
| AA Mutation | p.Arg201His(p.R201H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000246635 |
| Start | 41502748:41502748(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.962T>C |
| AA Mutation | p.Ile321Thr(p.I321T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000246635 |
| Start | 41502575:41502575(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs759178223 |
| CDS Mutation | c.1043C>T |
| AA Mutation | p.Thr348Met(p.T348M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000246635 |
| Start | 41505064:41505064(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs777961602 |
| CDS Mutation | c.487C>T |
| AA Mutation | p.Arg163Trp(p.R163W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000246635 |
| Start | 41505178:41505178(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.373C>A |
| AA Mutation | p.Leu125Met(p.L125M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000246635 |
| Start | 41505142:41505142(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs142183272 |
| CDS Mutation | c.409C>T |
| AA Mutation | p.Arg137Cys(p.R137C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000246635 |
| Start | 41502590:41502590(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs199762312 |
| CDS Mutation | c.1028C>T |
| AA Mutation | p.Ala343Val(p.A343V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000246635 |
| Start | 41503054:41503054(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.780G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000246635 |
| Start | 41503404:41503404(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs147005767 |
| CDS Mutation | c.618C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |