Primary Site >> Stomach Cancer
Gene >> NPHS1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000378910 |
| Start | 35848115:35848115(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs772461570 |
| CDS Mutation | c.1366C>T |
| AA Mutation | p.Arg456Trp(p.R456W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000378910 |
| Start | 35831137:35831137(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3397A>C |
| AA Mutation | p.Thr1133Pro(p.T1133P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000378910 |
| Start | 35849125:35849125(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs769782457 |
| CDS Mutation | c.863C>T |
| AA Mutation | p.Ala288Val(p.A288V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000378910 |
| Start | 35848397:35848397(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1171G>A |
| AA Mutation | p.Gly391Arg(p.G391R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000378910 |
| Start | 35830853:35830853(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3585A>C |
| AA Mutation | p.Glu1195Asp(p.E1195D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000378910 |
| Start | 35844123:35844123(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2192G>A |
| AA Mutation | p.Arg731Gln(p.R731Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000378910 |
| Start | 35826571:35826571(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3669C>A |
| AA Mutation | p.Asp1223Glu(p.D1223E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000378910 |
| Start | 35845421:35845421(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1877A>G |
| AA Mutation | p.His626Arg(p.H626R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000378910 |
| Start | 35842464:35842464(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2421A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000378910 |
| Start | 35849133:35849133(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs775775612 |
| CDS Mutation | c.855G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000378910 |
| Start | 35849136:35849136(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs763233132 |
| CDS Mutation | c.852G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000378910 |
| Start | 35850992:35850992(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs533934522 |
| CDS Mutation | c.495G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000378910 |
| Start | 35831108:35831108(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3426G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000378910 |
| Start | 35841770:35841770(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2760T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000378910 |
| Start | 35851338:35851338(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs145630223 |
| CDS Mutation | c.321G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |