Primary Site >> Stomach Cancer
Gene >> ZFP64
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000361387 |
| Start | 52084855:52084855(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1640G>T |
| AA Mutation | p.Arg547Met(p.R547M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000216923 |
| Start | 52160303:52160303(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.583C>T |
| AA Mutation | p.Arg195Trp(p.R195W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000216923 |
| Start | 52152505:52152505(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs758754357 |
| CDS Mutation | c.1687G>A |
| AA Mutation | p.Ala563Thr(p.A563T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000361387 |
| Start | 52084828:52084828(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs758774464 |
| CDS Mutation | c.1667C>T |
| AA Mutation | p.Ala556Val(p.A556V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000361387 |
| Start | 52084768:52084768(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1727C>T |
| AA Mutation | p.Thr576Met(p.T576M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000361387 |
| Start | 52085060:52085060(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs371226164 |
| CDS Mutation | c.1435C>T |
| AA Mutation | p.Arg479Trp(p.R479W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000361387 |
| Start | 52088488:52088488(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs760668340 |
| CDS Mutation | c.1132C>T |
| AA Mutation | p.Arg378Trp(p.R378W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000361387 |
| Start | 52084871:52084871(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs562200956 |
| CDS Mutation | c.1624G>A |
| AA Mutation | p.Val542Ile(p.V542I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000361387 |
| Start | 52098524:52098524(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs199967473 |
| CDS Mutation | c.827C>T |
| AA Mutation | p.Pro276Leu(p.P276L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000216923 |
| Start | 52152174:52152174(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2018T>A |
| AA Mutation | p.Leu673His(p.L673H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000361387 |
| Start | 52088487:52088487(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs775231013 |
| CDS Mutation | c.1133G>A |
| AA Mutation | p.Arg378Gln(p.R378Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000216923 |
| Start | 52152493:52152493(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1699C>T |
| AA Mutation | p.Pro567Ser(p.P567S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000216923 |
| Start | 52152645:52152645(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1547C>G |
| AA Mutation | p.Ala516Gly(p.A516G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000216923 |
| Start | 52152166:52152166(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs770091651 |
| CDS Mutation | c.2026G>A |
| AA Mutation | p.Ala676Thr(p.A676T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000361387 |
| Start | 52084895:52084895(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1600C>T |
| AA Mutation | p.Arg534Trp(p.R534W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000361387 |
| Start | 52088413:52088413(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs373948550 |
| CDS Mutation | c.1207G>A |
| AA Mutation | p.Val403Ile(p.V403I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000216923 |
| Start | 52153391:52153391(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.801G>C |
| AA Mutation | p.Lys267Asn(p.K267N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000216923 |
| Start | 52152282:52152282(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1910A>G |
| AA Mutation | p.Asn637Ser(p.N637S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000361387 |
| Start | 52084933:52084933(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1562G>T |
| AA Mutation | p.Arg521Leu(p.R521L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000361387 |
| Start | 52088434:52088434(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1186C>T |
| AA Mutation | p.Arg396Cys(p.R396C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000361387 |
| Start | 52088607:52088607(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1013G>A |
| AA Mutation | p.Cys338Tyr(p.C338Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000216923 |
| Start | 52153106:52153106(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1086G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000361387 |
| Start | 52084872:52084872(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs773709861 |
| CDS Mutation | c.1623C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000361387 |
| Start | 52085130:52085130(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1365G>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 25 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000216923 |
| Start | 52153325:52153325(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs771173936 |
| CDS Mutation | c.867C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 26 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000361387 |
| Start | 52084974:52084974(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs747815249 |
| CDS Mutation | c.1521G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 27 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000216923 |
| Start | 52152902:52152902(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs777236119 |
| CDS Mutation | c.1290C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 28 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000216923 |
| Start | 52153280:52153280(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.912G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 29 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000216923 |
| Start | 52152854:52152854(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1338G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 30 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000216923 |
| Start | 52153187:52153187(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1005C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 31 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000361387 |
| Start | 52085184:52085184(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1311G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 32 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000361387 |
| Start | 52085181:52085181(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1314G>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 33 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000216923 |
| Start | 52160256:52160256(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs140782754 |
| CDS Mutation | c.630C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 34 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000361387 |
| Start | 52084635:52084635(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs751150706 |
| CDS Mutation | c.1860C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 35 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000361387 |
| Start | 52088633:52088633(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs776477749 |
| CDS Mutation | c.987G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 36 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000361387 |
| Start | 52088561:52088561(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1059C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 37 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000361387 |
| Start | 52084740:52084740(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs765657938 |
| CDS Mutation | c.1755C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 38 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000361387 |
| Start | 52085222:52085222(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1273delA |
| AA Mutation | p.Ile425SerfsTer5(p.I425Sfs*5) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 39 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000371523 |
| Start | 52105138:52105138(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.100delG |
| AA Mutation | p.Glu34SerfsTer62(p.E34Sfs*62) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 40 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000361387 |
| Start | 52085180:52085180(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1315G>T |
| AA Mutation | p.Glu439Ter(p.E439*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 41 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000216923 |
| Start | 52152536:52152537(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.1654_1655dupCC |
| AA Mutation | p.Gln553LeufsTer13(p.Q553Lfs*13) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |