Primary Site >> Stomach Cancer
Gene >> WWC3
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000380861 |
| Start | 10126239:10126239(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs748994685 |
| CDS Mutation | c.2039C>T |
| AA Mutation | p.Ala680Val(p.A680V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000380861 |
| Start | 10126152:10126152(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1952C>T |
| AA Mutation | p.Thr651Met(p.T651M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000380861 |
| Start | 10078865:10078865(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs762106268 |
| CDS Mutation | c.287G>A |
| AA Mutation | p.Arg96His(p.R96H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000380861 |
| Start | 10109837:10109837(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.791C>T |
| AA Mutation | p.Ala264Val(p.A264V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000380861 |
| Start | 10117275:10117275(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1216G>A |
| AA Mutation | p.Glu406Lys(p.E406K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000380861 |
| Start | 10136648:10136648(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2779A>T |
| AA Mutation | p.Ser927Cys(p.S927C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000380861 |
| Start | 10128090:10128090(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs138880852 |
| CDS Mutation | c.2209C>T |
| AA Mutation | p.Arg737Trp(p.R737W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000380861 |
| Start | 10117162:10117162(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1103G>A |
| AA Mutation | p.Ser368Asn(p.S368N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000380861 |
| Start | 10090779:10090779(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201678620 |
| CDS Mutation | c.386G>A |
| AA Mutation | p.Arg129Gln(p.R129Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000380861 |
| Start | 10090869:10090869(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.476C>T |
| AA Mutation | p.Thr159Ile(p.T159I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000380861 |
| Start | 10109989:10109989(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.943C>T |
| AA Mutation | p.Arg315Trp(p.R315W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000380861 |
| Start | 10078835:10078835(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.257C>A |
| AA Mutation | p.Pro86Gln(p.P86Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000380861 |
| Start | 10139501:10139501(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3173G>T |
| AA Mutation | p.Gly1058Val(p.G1058V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000380861 |
| Start | 10117293:10117293(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs776295076 |
| CDS Mutation | c.1234C>T |
| AA Mutation | p.Arg412Cys(p.R412C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000380861 |
| Start | 10079789:10079789(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.362T>C |
| AA Mutation | p.Val121Ala(p.V121A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000380861 |
| Start | 10109839:10109839(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.793G>A |
| AA Mutation | p.Glu265Lys(p.E265K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000380861 |
| Start | 10109917:10109917(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs756780045 |
| CDS Mutation | c.871C>T |
| AA Mutation | p.Arg291Cys(p.R291C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000380861 |
| Start | 10122619:10122619(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1631C>A |
| AA Mutation | p.Thr544Lys(p.T544K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000380861 |
| Start | 10138931:10138931(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs377116582 |
| CDS Mutation | c.3079C>T |
| AA Mutation | p.Arg1027Trp(p.R1027W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000380861 |
| Start | 10117165:10117165(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs755281894 |
| CDS Mutation | c.1106G>A |
| AA Mutation | p.Arg369His(p.R369H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000380861 |
| Start | 10124302:10124302(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1789G>A |
| AA Mutation | p.Ala597Thr(p.A597T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000380861 |
| Start | 10138849:10138849(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs772592126 |
| CDS Mutation | c.2997C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000380861 |
| Start | 10117271:10117271(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs143647120 |
| CDS Mutation | c.1212C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000380861 |
| Start | 10125090:10125090(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs184706668 |
| CDS Mutation | c.1893G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 25 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000380861 |
| Start | 10134514:10134514(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.2681delG |
| AA Mutation | p.Arg894GlnfsTer90(p.R894Qfs*90) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |