Primary Site >> Stomach Cancer
Gene >> CD44
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000428726 |
| Start | 35190038:35190038(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs767614676 |
| CDS Mutation | c.640G>A |
| AA Mutation | p.Asp214Asn(p.D214N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000428726 |
| Start | 35198197:35198197(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.873T>G |
| AA Mutation | p.Ser291Arg(p.S291R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000428726 |
| Start | 35229205:35229205(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs369496409 |
| CDS Mutation | c.2101G>A |
| AA Mutation | p.Gly701Arg(p.G701R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000428726 |
| Start | 35176613:35176613(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.106G>A |
| AA Mutation | p.Val36Met(p.V36M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000428726 |
| Start | 35208204:35208204(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs147167567 |
| CDS Mutation | c.1514C>T |
| AA Mutation | p.Thr505Met(p.T505M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000428726 |
| Start | 35211435:35211435(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1796A>G |
| AA Mutation | p.Asn599Ser(p.N599S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000428726 |
| Start | 35201711:35201711(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1077G>C |
| AA Mutation | p.Trp359Cys(p.W359C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000428726 |
| Start | 35198176:35198176(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.852T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000428726 |
| Start | 35176591:35176591(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.84C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000428726 |
| Start | 35190034:35190034(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.636C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000428726 |
| Start | 35176612:35176612(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs749053466 |
| CDS Mutation | c.105C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000428726 |
| Start | 35221682:35221682(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1974G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000428726 |
| Start | 35180377:35180377(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.337C>T |
| AA Mutation | p.Gln113Ter(p.Q113*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | splice_donor_variant |
| Transcription ID | ENST00000428726 |
| Start | 35208207:35208207(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs141953333 |
| CDS Mutation | c.1516+1G>A |
| Mutation Classification | Splice_Site |
| Feature Type | Transcript |