Primary Site >> Stomach Cancer
Gene >> MUTYH
| ID | 1 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000372098 |
| Start | 45333415:45333415(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs373766973 |
| CDS Mutation | c.337C>T |
| AA Mutation | p.Arg113Trp(p.R113W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000372098 |
| Start | 45332191:45332191(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.899A>G |
| AA Mutation | p.Glu300Gly(p.E300G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000372098 |
| Start | 45332037:45332037(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.974A>G |
| AA Mutation | p.Asp325Gly(p.D325G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000372098 |
| Start | 45333147:45333147(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.403C>A |
| AA Mutation | p.Gln135Lys(p.Q135K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000372098 |
| Start | 45333471:45333471(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs755653922 |
| CDS Mutation | c.281G>A |
| AA Mutation | p.Arg94Gln(p.R94Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000372098 |
| Start | 45332278:45332278(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs149866955 |
| CDS Mutation | c.812G>A |
| AA Mutation | p.Arg271Gln(p.R271Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000372098 |
| Start | 45333500:45333500(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.252C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000372098 |
| Start | 45332483:45332483(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs780747266 |
| CDS Mutation | c.687C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000372098 |
| Start | 45332668:45332668(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.587delG |
| AA Mutation | p.Gly196AlafsTer41(p.G196Afs*41) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |