Primary Site >> Stomach Cancer
Gene >> CTNNA1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000302763 |
| Start | 138934046:138934046(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2678C>T |
| AA Mutation | p.Pro893Leu(p.P893L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000302763 |
| Start | 138932645:138932645(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2366A>G |
| AA Mutation | p.Gln789Arg(p.Q789R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000302763 |
| Start | 138932654:138932654(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2375T>A |
| AA Mutation | p.Ile792Asn(p.I792N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000302763 |
| Start | 138930654:138930654(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2192G>A |
| AA Mutation | p.Arg731Gln(p.R731Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000302763 |
| Start | 138824618:138824618(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.677A>G |
| AA Mutation | p.Gln226Arg(p.Q226R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000302763 |
| Start | 138824737:138824737(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.796G>A |
| AA Mutation | p.Asp266Asn(p.D266N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000302763 |
| Start | 138930621:138930621(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2159G>A |
| AA Mutation | p.Cys720Tyr(p.C720Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000302763 |
| Start | 138824551:138824551(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs748407995 |
| CDS Mutation | c.610C>T |
| AA Mutation | p.Arg204Cys(p.R204C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000302763 |
| Start | 138783364:138783364(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs746832628 |
| CDS Mutation | c.293G>A |
| AA Mutation | p.Arg98Gln(p.R98Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000302763 |
| Start | 138930507:138930507(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2045C>T |
| AA Mutation | p.Ala682Val(p.A682V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000302763 |
| Start | 138933896:138933896(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2528A>G |
| AA Mutation | p.Tyr843Cys(p.Y843C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000302763 |
| Start | 138824586:138824586(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.645G>T |
| AA Mutation | p.Gln215His(p.Q215H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000302763 |
| Start | 138810196:138810196(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.460C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000302763 |
| Start | 138824757:138824757(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.816T>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000302763 |
| Start | 138783248:138783248(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.177T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000302763 |
| Start | 138917858:138917858(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1506C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000302763 |
| Start | 138917827:138917827(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.1479delA |
| AA Mutation | p.Lys493AsnfsTer31(p.K493Nfs*31) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000302763 |
| Start | 138930846:138930846(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.2213delA |
| AA Mutation | p.Asn738IlefsTer53(p.N738Ifs*53) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000302763 |
| Start | 138925266:138925266(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1761delT |
| AA Mutation | p.Phe587LeufsTer5(p.F587Lfs*5) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000302763 |
| Start | 138929264:138929277(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1921_1934delTCTGACTTTGAGAC |
| AA Mutation | p.Ser641ArgfsTer4(p.S641Rfs*4) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000302763 |
| Start | 138810121:138810121(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs758599826 |
| CDS Mutation | c.385C>T |
| AA Mutation | p.Arg129Ter(p.R129*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |