Primary Site >> Stomach Cancer
Gene >> SSH1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000326495 |
| Start | 108788172:108788172(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs756991636 |
| CDS Mutation | c.2966C>T |
| AA Mutation | p.Thr989Met(p.T989M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000326495 |
| Start | 108817093:108817093(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs199897989 |
| CDS Mutation | c.346C>T |
| AA Mutation | p.Arg116Cys(p.R116C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000326495 |
| Start | 108788007:108788007(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs375673898 |
| CDS Mutation | c.3131C>T |
| AA Mutation | p.Ser1044Leu(p.S1044L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000326495 |
| Start | 108788236:108788236(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2902A>T |
| AA Mutation | p.Thr968Ser(p.T968S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000326495 |
| Start | 108807796:108807796(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.568G>A |
| AA Mutation | p.Glu190Lys(p.E190K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000326495 |
| Start | 108788805:108788805(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2333C>T |
| AA Mutation | p.Ser778Leu(p.S778L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000326495 |
| Start | 108800804:108800804(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs755430218 |
| CDS Mutation | c.1124C>T |
| AA Mutation | p.Ala375Val(p.A375V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000326495 |
| Start | 108788432:108788432(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2706C>A |
| AA Mutation | p.Phe902Leu(p.F902L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000326495 |
| Start | 108799113:108799113(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs184372660 |
| CDS Mutation | c.1236C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000326495 |
| Start | 108792685:108792685(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200240565 |
| CDS Mutation | c.1494C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000326495 |
| Start | 108792660:108792660(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.1519delC |
| AA Mutation | p.Leu507SerfsTer62(p.L507Sfs*62) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000326495 |
| Start | 108800881:108800881(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.1047delT |
| AA Mutation | p.Pro350LeufsTer30(p.P350Lfs*30) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000326495 |
| Start | 108789139:108789139(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs753174548 |
| CDS Mutation | c.1999C>T |
| AA Mutation | p.Arg667Ter(p.R667*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |