Primary Site >> Stomach Cancer
Gene >> WNK2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000297954 |
| Start | 93293065:93293065(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5711C>T |
| AA Mutation | p.Thr1904Met(p.T1904M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000297954 |
| Start | 93299225:93299225(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs748545366 |
| CDS Mutation | c.6190G>A |
| AA Mutation | p.Gly2064Ser(p.G2064S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000297954 |
| Start | 93247606:93247606(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1606G>A |
| AA Mutation | p.Val536Met(p.V536M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000297954 |
| Start | 93261902:93261902(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs745454786 |
| CDS Mutation | c.3155C>T |
| AA Mutation | p.Pro1052Leu(p.P1052L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000297954 |
| Start | 93262054:93262054(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3307G>A |
| AA Mutation | p.Gly1103Arg(p.G1103R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000297954 |
| Start | 93267845:93267845(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3796G>T |
| AA Mutation | p.Asp1266Tyr(p.D1266Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000297954 |
| Start | 93289213:93289213(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs757583408 |
| CDS Mutation | c.4570G>A |
| AA Mutation | p.Gly1524Arg(p.G1524R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000297954 |
| Start | 93229868:93229868(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.854C>T |
| AA Mutation | p.Thr285Ile(p.T285I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000297954 |
| Start | 93229838:93229838(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.824C>T |
| AA Mutation | p.Thr275Met(p.T275M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000297954 |
| Start | 93185460:93185460(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs368882633 |
| CDS Mutation | c.531G>C |
| AA Mutation | p.Glu177Asp(p.E177D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000297954 |
| Start | 93292947:93292947(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs767135945 |
| CDS Mutation | c.5593G>A |
| AA Mutation | p.Val1865Met(p.V1865M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000297954 |
| Start | 93308438:93308438(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.6481G>A |
| AA Mutation | p.Asp2161Asn(p.D2161N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000297954 |
| Start | 93299253:93299253(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs776503070 |
| CDS Mutation | c.6218G>A |
| AA Mutation | p.Arg2073His(p.R2073H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000297954 |
| Start | 93234893:93234893(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1161G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000297954 |
| Start | 93289155:93289155(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4512C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000297954 |
| Start | 93259149:93259149(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs375757039 |
| CDS Mutation | c.2601G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000297954 |
| Start | 93293090:93293090(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.5736C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000297954 |
| Start | 93317889:93317889(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs750142295 |
| CDS Mutation | c.6756C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000297954 |
| Start | 93259032:93259032(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2484G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000297954 |
| Start | 93258963:93258963(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs753283002 |
| CDS Mutation | c.2415G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000297954 |
| Start | 93259119:93259119(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2571G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000297954 |
| Start | 93231011:93231011(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.978T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000297954 |
| Start | 93234827:93234827(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs550073972 |
| CDS Mutation | c.1095G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000297954 |
| Start | 93256980:93256980(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2223G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 25 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000297954 |
| Start | 93289074:93289074(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs771161796 |
| CDS Mutation | c.4431C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 26 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000297954 |
| Start | 93185553:93185553(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.624G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 27 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000297954 |
| Start | 93259317:93259317(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs147646744 |
| CDS Mutation | c.2769C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 28 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000297954 |
| Start | 93289203:93289203(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.4564delC |
| AA Mutation | p.His1522ThrfsTer104(p.H1522Tfs*104) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 29 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000297954 |
| Start | 93258952:93258952(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.2409delC |
| AA Mutation | p.Ile804SerfsTer35(p.I804Sfs*35) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 30 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000297954 |
| Start | 93259137:93259137(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.2594delC |
| AA Mutation | p.Pro865LeufsTer25(p.P865Lfs*25) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 31 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000297954 |
| Start | 93259328:93259328(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.2785delC |
| AA Mutation | p.His929IlefsTer7(p.H929Ifs*7) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 32 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000297954 |
| Start | 93257069:93257069(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.2316delC |
| AA Mutation | p.Ala773LeufsTer3(p.A773Lfs*3) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 33 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000297954 |
| Start | 93268649:93268650(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.3938dupT |
| AA Mutation | p.Ile1314HisfsTer7(p.I1314Hfs*7) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |
| ID | 34 |
| Mutation Consequence | splice_donor_variant;coding_sequence_variant;intron_variant |
| Transcription ID | ENST00000297954 |
| Start | 93267916:93267938(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.3867+2_3867+24delTGAGGTTGTGAAATCCGGGGTGG |
| Mutation Classification | Splice_Site |
| Feature Type | Transcript |
| ID | 35 |
| Mutation Consequence | inframe_insertion |
| Transcription ID | ENST00000297954 |
| Start | 93185457:93185458(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.538_546dupGAGGACGAC |
| AA Mutation | p.Glu180_Asp182dup(p.E180_D182dup) |
| Mutation Classification | In_Frame_Ins |
| Feature Type | Transcript |