Primary Site >> Stomach Cancer
Gene >> ADAM15
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356955 |
| Start | 155056219:155056219(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs779369135 |
| CDS Mutation | c.884G>A |
| AA Mutation | p.Arg295Gln(p.R295Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356955 |
| Start | 155054352:155054352(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.458T>C |
| AA Mutation | p.Leu153Pro(p.L153P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356955 |
| Start | 155061922:155061922(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs758735866 |
| CDS Mutation | c.2371C>T |
| AA Mutation | p.Pro791Ser(p.P791S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356955 |
| Start | 155057938:155057938(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1504C>T |
| AA Mutation | p.Pro502Ser(p.P502S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356955 |
| Start | 155060267:155060267(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2131C>A |
| AA Mutation | p.Leu711Ile(p.L711I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356955 |
| Start | 155057857:155057857(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1423C>A |
| AA Mutation | p.Pro475Thr(p.P475T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000356955 |
| Start | 155057642:155057642(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs377522696 |
| CDS Mutation | c.1329C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000356955 |
| Start | 155054185:155054185(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.378T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000356955 |
| Start | 155055813:155055813(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.636C>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000356955 |
| Start | 155056997:155056997(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs754264835 |
| CDS Mutation | c.1044T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000356955 |
| Start | 155060306:155060306(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs142428973 |
| CDS Mutation | c.2170C>T |
| AA Mutation | p.Arg724Ter(p.R724*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |