Primary Site >> Stomach Cancer
Gene >> STARD13
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000336934 |
| Start | 33129434:33129434(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1243C>A |
| AA Mutation | p.Leu415Ile(p.L415I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000336934 |
| Start | 33167558:33167558(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.234A>C |
| AA Mutation | p.Leu78Phe(p.L78F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000336934 |
| Start | 33130138:33130138(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs149234861 |
| CDS Mutation | c.539C>T |
| AA Mutation | p.Thr180Met(p.T180M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000336934 |
| Start | 33126088:33126088(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2075T>C |
| AA Mutation | p.Leu692Pro(p.L692P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000336934 |
| Start | 33130010:33130010(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.667C>A |
| AA Mutation | p.Leu223Met(p.L223M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000336934 |
| Start | 33118124:33118124(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2222A>T |
| AA Mutation | p.Asp741Val(p.D741V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000336934 |
| Start | 33129040:33129040(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201324553 |
| CDS Mutation | c.1637C>T |
| AA Mutation | p.Thr546Met(p.T546M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000336934 |
| Start | 33110873:33110873(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2642C>T |
| AA Mutation | p.Ser881Leu(p.S881L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000336934 |
| Start | 33285515:33285515(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.124A>C |
| AA Mutation | p.Ser42Arg(p.S42R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000336934 |
| Start | 33127400:33127400(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1895C>T |
| AA Mutation | p.Ser632Phe(p.S632F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000336934 |
| Start | 33110014:33110014(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2906G>T |
| AA Mutation | p.Arg969Leu(p.R969L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000336934 |
| Start | 33127427:33127427(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1868G>A |
| AA Mutation | p.Arg623His(p.R623H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000336934 |
| Start | 33129039:33129039(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs541502281 |
| CDS Mutation | c.1638G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000336934 |
| Start | 33112831:33112831(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs748109327 |
| CDS Mutation | c.2382C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000336934 |
| Start | 33167567:33167567(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs763387562 |
| CDS Mutation | c.225C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000336934 |
| Start | 33127423:33127423(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1872C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000336934 |
| Start | 33130128:33130128(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.549T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000336934 |
| Start | 33112795:33112795(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs145394840 |
| CDS Mutation | c.2418G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |