Primary Site >> Stomach Cancer
Gene >> SH3PXD2A
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369774 |
| Start | 103612931:103612931(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs771136503 |
| CDS Mutation | c.1180G>A |
| AA Mutation | p.Val394Ile(p.V394I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369774 |
| Start | 103601890:103601890(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3328T>C |
| AA Mutation | p.Tyr1110His(p.Y1110H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369774 |
| Start | 103603420:103603420(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs772194389 |
| CDS Mutation | c.1798C>T |
| AA Mutation | p.Arg600Trp(p.R600W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369774 |
| Start | 103602631:103602631(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs766798828 |
| CDS Mutation | c.2587G>A |
| AA Mutation | p.Ala863Thr(p.A863T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369774 |
| Start | 103602126:103602126(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs553818409 |
| CDS Mutation | c.3092G>A |
| AA Mutation | p.Arg1031His(p.R1031H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369774 |
| Start | 103602462:103602462(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2756A>G |
| AA Mutation | p.Asn919Ser(p.N919S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369774 |
| Start | 103602291:103602291(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs373805914 |
| CDS Mutation | c.2927C>T |
| AA Mutation | p.Ala976Val(p.A976V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369774 |
| Start | 103601907:103601907(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3311A>G |
| AA Mutation | p.Asn1104Ser(p.N1104S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369774 |
| Start | 103767136:103767136(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.187G>T |
| AA Mutation | p.Gly63Cys(p.G63C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369774 |
| Start | 103617216:103617216(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs577209053 |
| CDS Mutation | c.901G>A |
| AA Mutation | p.Glu301Lys(p.E301K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369774 |
| Start | 103603647:103603647(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs773819318 |
| CDS Mutation | c.1571C>T |
| AA Mutation | p.Pro524Leu(p.P524L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000369774 |
| Start | 103603712:103603712(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs748216122 |
| CDS Mutation | c.1506C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000369774 |
| Start | 103602521:103602521(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2697C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000369774 |
| Start | 103601932:103601932(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.3286delG |
| AA Mutation | p.Val1096CysfsTer22(p.V1096Cfs*22) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000369774 |
| Start | 103603243:103603244(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.1974dupC |
| AA Mutation | p.Lys659GlnfsTer83(p.K659Qfs*83) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000369774 |
| Start | 103724339:103724340(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | rs777796332 |
| CDS Mutation | c.328dupC |
| AA Mutation | p.His110ProfsTer6(p.H110Pfs*6) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |