Primary Site >> Stomach Cancer
Gene >> AGL
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000294724 |
| Start | 99874792:99874792(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs557516658 |
| CDS Mutation | c.1064C>T |
| AA Mutation | p.Thr355Met(p.T355M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000294724 |
| Start | 99864502:99864502(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.577A>G |
| AA Mutation | p.Thr193Ala(p.T193A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000294724 |
| Start | 99913680:99913680(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs769401330 |
| CDS Mutation | c.4103C>T |
| AA Mutation | p.Ala1368Val(p.A1368V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000294724 |
| Start | 99881617:99881617(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2234C>A |
| AA Mutation | p.Ala745Asp(p.A745D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000294724 |
| Start | 99921632:99921632(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4580A>G |
| AA Mutation | p.Glu1527Gly(p.E1527G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000294724 |
| Start | 99864436:99864436(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.511T>C |
| AA Mutation | p.Ser171Pro(p.S171P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000294724 |
| Start | 99888061:99888061(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2765G>A |
| AA Mutation | p.Cys922Tyr(p.C922Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000294724 |
| Start | 99884613:99884613(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs776599112 |
| CDS Mutation | c.2591G>A |
| AA Mutation | p.Arg864Gln(p.R864Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000294724 |
| Start | 99879989:99879989(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1678A>C |
| AA Mutation | p.Ser560Arg(p.S560R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000294724 |
| Start | 99912453:99912453(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3885C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000294724 |
| Start | 99916663:99916663(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4413G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000294724 |
| Start | 99915441:99915441(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.4221delA |
| AA Mutation | p.Lys1407AsnfsTer8(p.K1407Nfs*8) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000294724 |
| Start | 99870764:99870764(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs755747010 |
| CDS Mutation | c.853C>T |
| AA Mutation | p.Arg285Ter(p.R285*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000294724 |
| Start | 99874695:99874695(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs757987101 |
| CDS Mutation | c.967C>T |
| AA Mutation | p.Arg323Ter(p.R323*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |