Primary Site >> Stomach Cancer
Gene >> AKAP12
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000253332 |
| Start | 151350255:151350255(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs143476871 |
| CDS Mutation | c.1864C>T |
| AA Mutation | p.Arg622Cys(p.R622C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000253332 |
| Start | 151353562:151353562(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5171C>G |
| AA Mutation | p.Thr1724Ser(p.T1724S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000253332 |
| Start | 151352823:151352823(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs775450726 |
| CDS Mutation | c.4432G>A |
| AA Mutation | p.Asp1478Asn(p.D1478N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000253332 |
| Start | 151353664:151353664(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.5273C>T |
| AA Mutation | p.Ala1758Val(p.A1758V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000253332 |
| Start | 151351237:151351237(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs766910226 |
| CDS Mutation | c.2846C>T |
| AA Mutation | p.Thr949Met(p.T949M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000253332 |
| Start | 151351397:151351397(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3006G>T |
| AA Mutation | p.Met1002Ile(p.M1002I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000253332 |
| Start | 151351090:151351090(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs771644564 |
| CDS Mutation | c.2699C>T |
| AA Mutation | p.Thr900Met(p.T900M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000253332 |
| Start | 151350127:151350127(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1736T>C |
| AA Mutation | p.Leu579Pro(p.L579P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000253332 |
| Start | 151353207:151353207(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4816C>G |
| AA Mutation | p.Gln1606Glu(p.Q1606E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000253332 |
| Start | 151349314:151349314(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs141729078 |
| CDS Mutation | c.923G>A |
| AA Mutation | p.Arg308His(p.R308H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000253332 |
| Start | 151351731:151351731(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3340C>A |
| AA Mutation | p.Gln1114Lys(p.Q1114K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000253332 |
| Start | 151353148:151353148(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4757A>G |
| AA Mutation | p.Asp1586Gly(p.D1586G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000253332 |
| Start | 151349109:151349109(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs552053449 |
| CDS Mutation | c.718G>A |
| AA Mutation | p.Glu240Lys(p.E240K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000253332 |
| Start | 151351047:151351047(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs149275104 |
| CDS Mutation | c.2656G>A |
| AA Mutation | p.Glu886Lys(p.E886K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000253332 |
| Start | 151349877:151349877(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs374740675 |
| CDS Mutation | c.1486G>A |
| AA Mutation | p.Val496Ile(p.V496I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000253332 |
| Start | 151350312:151350312(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs753094802 |
| CDS Mutation | c.1921G>A |
| AA Mutation | p.Ala641Thr(p.A641T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000253332 |
| Start | 151353076:151353076(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4685T>C |
| AA Mutation | p.Val1562Ala(p.V1562A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000253332 |
| Start | 151348829:151348829(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs561437815 |
| CDS Mutation | c.438C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000253332 |
| Start | 151349489:151349489(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs752192182 |
| CDS Mutation | c.1098C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000253332 |
| Start | 151353197:151353197(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4806G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000253332 |
| Start | 151350218:151350218(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1827C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000253332 |
| Start | 151352312:151352312(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3921A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000253332 |
| Start | 151351229:151351229(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2838A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000253332 |
| Start | 151351475:151351475(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3084C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 25 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000253332 |
| Start | 151350080:151350080(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs750541234 |
| CDS Mutation | c.1689C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 26 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000253332 |
| Start | 151349187:151349188(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.797_798delAA |
| AA Mutation | p.Lys266ArgfsTer12(p.K266Rfs*12) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 27 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000253332 |
| Start | 151351230:151351230(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.2844delC |
| AA Mutation | p.Thr949ArgfsTer23(p.T949Rfs*23) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 28 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000253332 |
| Start | 151352767:151352767(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.4382delA |
| AA Mutation | p.Asn1461MetfsTer26(p.N1461Mfs*26) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 29 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000253332 |
| Start | 151350831:151350831(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2440C>T |
| AA Mutation | p.Arg814Ter(p.R814*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 30 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000253332 |
| Start | 151351864:151351865(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.3479dupC |
| AA Mutation | p.Asp1161Ter(p.D1161*) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |
| ID | 31 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000253332 |
| Start | 151353145:151353146(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.4754_4755insAG |
| AA Mutation | p.Asp1586ValfsTer50(p.D1586Vfs*50) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |
| ID | 32 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000253332 |
| Start | 151351229:151351230(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | rs767490652 |
| CDS Mutation | c.2844dupC |
| AA Mutation | p.Thr949HisfsTer4(p.T949Hfs*4) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |