Primary Site >> Stomach Cancer
Gene >> DAO
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000228476 |
| Start | 108885112:108885112(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs551786568 |
| CDS Mutation | c.106G>A |
| AA Mutation | p.Ala36Thr(p.A36T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000228476 |
| Start | 108900501:108900501(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1010A>C |
| AA Mutation | p.Lys337Thr(p.K337T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000228476 |
| Start | 108899420:108899420(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs566264618 |
| CDS Mutation | c.857G>A |
| AA Mutation | p.Arg286His(p.R286H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000228476 |
| Start | 108885155:108885155(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.149G>A |
| AA Mutation | p.Gly50Asp(p.G50D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000228476 |
| Start | 108898755:108898755(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.772A>G |
| AA Mutation | p.Thr258Ala(p.T258A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000228476 |
| Start | 108885040:108885040(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs373913310 |
| CDS Mutation | c.34G>A |
| AA Mutation | p.Gly12Arg(p.G12R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000228476 |
| Start | 108893013:108893013(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.484C>T |
| AA Mutation | p.Arg162Trp(p.R162W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000228476 |
| Start | 108900431:108900431(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.940T>C |
| AA Mutation | p.Tyr314His(p.Y314H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000228476 |
| Start | 108894284:108894284(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs373110648 |
| CDS Mutation | c.529G>A |
| AA Mutation | p.Val177Met(p.V177M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000228476 |
| Start | 108899398:108899398(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs745766982 |
| CDS Mutation | c.835C>T |
| AA Mutation | p.Arg279Ter(p.R279*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000228476 |
| Start | 108889520:108889520(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.361G>T |
| AA Mutation | p.Glu121Ter(p.E121*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000228476 |
| Start | 108897049:108897050(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.663_664dupAG |
| AA Mutation | p.Gly222GlufsTer30(p.G222Efs*30) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000228476 |
| Start | 108889511:108889512(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.357dupC |
| AA Mutation | p.Arg120GlnfsTer31(p.R120Qfs*31) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | splice_donor_variant |
| Transcription ID | ENST00000228476 |
| Start | 108885201:108885201(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs762930737 |
| CDS Mutation | c.194+1G>A |
| Mutation Classification | Splice_Site |
| Feature Type | Transcript |