Primary Site >> Stomach Cancer
Gene >> PEAK1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000312493 |
| Start | 77181227:77181227(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.700G>A |
| AA Mutation | p.Glu234Lys(p.E234K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000312493 |
| Start | 77115151:77115151(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4246G>C |
| AA Mutation | p.Asp1416His(p.D1416H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000312493 |
| Start | 77181594:77181594(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.333G>C |
| AA Mutation | p.Leu111Phe(p.L111F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000312493 |
| Start | 77178810:77178810(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3117G>T |
| AA Mutation | p.Gln1039His(p.Q1039H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000312493 |
| Start | 77181037:77181037(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs759331417 |
| CDS Mutation | c.890G>A |
| AA Mutation | p.Arg297Gln(p.R297Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000312493 |
| Start | 77115178:77115178(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4219G>C |
| AA Mutation | p.Asp1407His(p.D1407H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000312493 |
| Start | 77179274:77179274(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2653C>A |
| AA Mutation | p.Leu885Ile(p.L885I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000312493 |
| Start | 77178793:77178793(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3134T>G |
| AA Mutation | p.Leu1045Arg(p.L1045R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000312493 |
| Start | 77180602:77180602(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1325A>T |
| AA Mutation | p.Asp442Val(p.D442V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000312493 |
| Start | 77179018:77179018(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs745782057 |
| CDS Mutation | c.2909G>A |
| AA Mutation | p.Arg970His(p.R970H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000312493 |
| Start | 77114796:77114796(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4601A>G |
| AA Mutation | p.Gln1534Arg(p.Q1534R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000312493 |
| Start | 77180084:77180084(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs536431798 |
| CDS Mutation | c.1843A>G |
| AA Mutation | p.Thr615Ala(p.T615A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000312493 |
| Start | 77181555:77181555(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.372A>C |
| AA Mutation | p.Glu124Asp(p.E124D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000312493 |
| Start | 77133028:77133028(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4054C>T |
| AA Mutation | p.Pro1352Ser(p.P1352S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000312493 |
| Start | 77180009:77180009(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1918A>G |
| AA Mutation | p.Ile640Val(p.I640V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000312493 |
| Start | 77181661:77181661(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.266T>C |
| AA Mutation | p.Leu89Pro(p.L89P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000312493 |
| Start | 77133167:77133167(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs757277454 |
| CDS Mutation | c.3915C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000312493 |
| Start | 77181041:77181041(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.886C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000312493 |
| Start | 77114384:77114384(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs199706567 |
| CDS Mutation | c.5013C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000312493 |
| Start | 77133713:77133713(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3369A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000312493 |
| Start | 77181723:77181723(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.204delA |
| AA Mutation | p.Lys68AsnfsTer4(p.K68Nfs*4) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000312493 |
| Start | 77133211:77133211(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3871C>T |
| AA Mutation | p.Arg1291Ter(p.R1291*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000312493 |
| Start | 77181038:77181038(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs770000942 |
| CDS Mutation | c.889C>T |
| AA Mutation | p.Arg297Ter(p.R297*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |