Primary Site >> Stomach Cancer
Gene >> KRT20
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000167588 |
| Start | 40878193:40878193(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1091A>G |
| AA Mutation | p.Glu364Gly(p.E364G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000167588 |
| Start | 40885094:40885094(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.92C>T |
| AA Mutation | p.Thr31Met(p.T31M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000167588 |
| Start | 40880652:40880652(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.592A>G |
| AA Mutation | p.Asn198Asp(p.N198D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000167588 |
| Start | 40878325:40878325(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs545785377 |
| CDS Mutation | c.959G>A |
| AA Mutation | p.Arg320His(p.R320H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000167588 |
| Start | 40880183:40880183(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs539218286 |
| CDS Mutation | c.709G>A |
| AA Mutation | p.Val237Ile(p.V237I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000167588 |
| Start | 40884841:40884841(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs754052121 |
| CDS Mutation | c.345C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000167588 |
| Start | 40884868:40884868(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs189056319 |
| CDS Mutation | c.318C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |