Primary Site >> Stomach Cancer
Gene >> SARS2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000221431 |
| Start | 38919766:38919766(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs777764275 |
| CDS Mutation | c.755G>A |
| AA Mutation | p.Arg252His(p.R252H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000221431 |
| Start | 38921404:38921404(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs141084630 |
| CDS Mutation | c.577G>A |
| AA Mutation | p.Gly193Arg(p.G193R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000221431 |
| Start | 38916090:38916090(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1294C>T |
| AA Mutation | p.Arg432Cys(p.R432C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000221431 |
| Start | 38921634:38921634(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.427C>T |
| AA Mutation | p.Arg143Trp(p.R143W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000221431 |
| Start | 38917728:38917728(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1156T>G |
| AA Mutation | p.Phe386Val(p.F386V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000221431 |
| Start | 38915665:38915665(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1498T>C |
| AA Mutation | p.Tyr500His(p.Y500H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000221431 |
| Start | 38921639:38921639(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs779303412 |
| CDS Mutation | c.422G>A |
| AA Mutation | p.Arg141His(p.R141H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000221431 |
| Start | 38921421:38921421(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.560G>A |
| AA Mutation | p.Arg187Gln(p.R187Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000221431 |
| Start | 38916040:38916040(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs17854237 |
| CDS Mutation | c.1344C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |