Primary Site >> Stomach Cancer
Gene >> SRCIN1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000617146 |
| Start | 38564216:38564216(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.443C>T |
| AA Mutation | p.Ser148Leu(p.S148L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000617146 |
| Start | 38561541:38561541(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs756455679 |
| CDS Mutation | c.1622C>T |
| AA Mutation | p.Ser541Leu(p.S541L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000617146 |
| Start | 38551965:38551965(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2648T>G |
| AA Mutation | p.Leu883Arg(p.L883R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000617146 |
| Start | 38552488:38552488(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2439G>T |
| AA Mutation | p.Lys813Asn(p.K813N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000617146 |
| Start | 38549069:38549069(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3104C>T |
| AA Mutation | p.Ser1035Leu(p.S1035L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000617146 |
| Start | 38552042:38552042(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs202075131 |
| CDS Mutation | c.2571C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000617146 |
| Start | 38551970:38551970(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2643C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000617146 |
| Start | 38551345:38551345(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2772G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000617146 |
| Start | 38561579:38561579(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1584C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000617146 |
| Start | 38562839:38562842(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.819_822delCAAC |
| AA Mutation | p.Asn274GlyfsTer100(p.N274Gfs*100) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000617146 |
| Start | 38551216:38551216(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.2901delC |
| AA Mutation | p.Lys968ArgfsTer23(p.K968Rfs*23) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000617146 |
| Start | 38552018:38552018(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.2595delC |
| AA Mutation | p.Ser866AlafsTer4(p.S866Afs*4) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000617146 |
| Start | 38551185:38551185(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.2932delC |
| AA Mutation | p.Arg978GlufsTer13(p.R978Efs*13) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000617146 |
| Start | 38551185:38551185(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2932C>T |
| AA Mutation | p.Arg978Ter(p.R978*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000617146 |
| Start | 38551184:38551185(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.2932dupC |
| AA Mutation | p.Arg978ProfsTer12(p.R978Pfs*12) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | splice_donor_variant |
| Transcription ID | ENST00000617146 |
| Start | 38561462:38561462(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1700+1G>C |
| Mutation Classification | Splice_Site |
| Feature Type | Transcript |