Primary Site >> Stomach Cancer
Gene >> RTEL1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000370018 |
| Start | 63692958:63692958(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs749800565 |
| CDS Mutation | c.2806G>A |
| AA Mutation | p.Gly936Ser(p.G936S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000370018 |
| Start | 63662860:63662860(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs750794827 |
| CDS Mutation | c.509G>A |
| AA Mutation | p.Arg170His(p.R170H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000370018 |
| Start | 63694901:63694901(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3270C>G |
| AA Mutation | p.Asp1090Glu(p.D1090E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000370018 |
| Start | 63661446:63661446(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201555555 |
| CDS Mutation | c.251G>A |
| AA Mutation | p.Arg84Gln(p.R84Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000370018 |
| Start | 63689784:63689784(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2060C>T |
| AA Mutation | p.Ala687Val(p.A687V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000370018 |
| Start | 63679914:63679914(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs765792997 |
| CDS Mutation | c.1103C>T |
| AA Mutation | p.Ser368Leu(p.S368L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000370018 |
| Start | 63694806:63694806(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs115303435 |
| CDS Mutation | c.3175G>A |
| AA Mutation | p.Ala1059Thr(p.A1059T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000370018 |
| Start | 63693248:63693248(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs146221660 |
| CDS Mutation | c.2957G>A |
| AA Mutation | p.Arg986Gln(p.R986Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000370018 |
| Start | 63661899:63661899(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.351G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000370018 |
| Start | 63694805:63694805(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs146247083 |
| CDS Mutation | c.3174C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000370018 |
| Start | 63689779:63689779(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2055G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000370018 |
| Start | 63693174:63693174(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2883G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000370018 |
| Start | 63694898:63694898(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs370637234 |
| CDS Mutation | c.3267C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000370018 |
| Start | 63661441:63661441(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs775247678 |
| CDS Mutation | c.246G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |