Primary Site >> Stomach Cancer
Gene >> ARNT2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000303329 |
| Start | 80580542:80580542(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs147344883 |
| CDS Mutation | c.1745C>T |
| AA Mutation | p.Pro582Leu(p.P582L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000303329 |
| Start | 80514369:80514369(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.841C>T |
| AA Mutation | p.His281Tyr(p.H281Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000303329 |
| Start | 80563194:80563194(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1271A>G |
| AA Mutation | p.Tyr424Cys(p.Y424C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000303329 |
| Start | 80593646:80593646(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2102A>G |
| AA Mutation | p.Tyr701Cys(p.Y701C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000303329 |
| Start | 80514394:80514394(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.866G>T |
| AA Mutation | p.Trp289Leu(p.W289L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000303329 |
| Start | 80514327:80514327(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.799C>A |
| AA Mutation | p.Leu267Ile(p.L267I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000303329 |
| Start | 80574166:80574166(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1335G>T |
| AA Mutation | p.Gln445His(p.Q445H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000303329 |
| Start | 80581315:80581315(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1829C>T |
| AA Mutation | p.Pro610Leu(p.P610L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000303329 |
| Start | 80470237:80470237(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.214G>A |
| AA Mutation | p.Glu72Lys(p.E72K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000303329 |
| Start | 80563116:80563116(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs754379136 |
| CDS Mutation | c.1193C>T |
| AA Mutation | p.Ser398Leu(p.S398L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000303329 |
| Start | 80450939:80450939(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs202043975 |
| CDS Mutation | c.91G>A |
| AA Mutation | p.Gly31Arg(p.G31R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000303329 |
| Start | 80575059:80575059(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1462T>C |
| AA Mutation | p.Ser488Pro(p.S488P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000303329 |
| Start | 80580529:80580529(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs144530385 |
| CDS Mutation | c.1732C>T |
| AA Mutation | p.Arg578Cys(p.R578C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000303329 |
| Start | 80508234:80508234(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.701G>A |
| AA Mutation | p.Arg234Gln(p.R234Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000303329 |
| Start | 80576885:80576885(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1533C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000303329 |
| Start | 80450911:80450911(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs745975276 |
| CDS Mutation | c.63G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |