Primary Site >> Stomach Cancer
Gene >> WASF3
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000335327 |
| Start | 26676649:26676649(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.641T>G |
| AA Mutation | p.Leu214Arg(p.L214R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000335327 |
| Start | 26682618:26682618(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs746475574 |
| CDS Mutation | c.995C>T |
| AA Mutation | p.Ala332Val(p.A332V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000335327 |
| Start | 26676558:26676558(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs373950661 |
| CDS Mutation | c.550C>T |
| AA Mutation | p.Arg184Cys(p.R184C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000335327 |
| Start | 26681151:26681151(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs762342891 |
| CDS Mutation | c.814G>A |
| AA Mutation | p.Val272Met(p.V272M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000335327 |
| Start | 26642386:26642386(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.116G>T |
| AA Mutation | p.Arg39Leu(p.R39L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000335327 |
| Start | 26685777:26685777(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs762162577 |
| CDS Mutation | c.1441C>T |
| AA Mutation | p.Arg481Cys(p.R481C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000335327 |
| Start | 26685810:26685810(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1474G>A |
| AA Mutation | p.Asp492Asn(p.D492N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000335327 |
| Start | 26676559:26676559(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.551G>A |
| AA Mutation | p.Arg184His(p.R184H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000335327 |
| Start | 26681197:26681197(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.860G>T |
| AA Mutation | p.Arg287Leu(p.R287L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000335327 |
| Start | 26681284:26681284(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.947C>A |
| AA Mutation | p.Ser316Tyr(p.S316Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000335327 |
| Start | 26685830:26685830(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs376926818 |
| CDS Mutation | c.1494C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000335327 |
| Start | 26682817:26682817(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1194G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000335327 |
| Start | 26682808:26682808(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs376560983 |
| CDS Mutation | c.1185G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000335327 |
| Start | 26682968:26682968(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1345C>T |
| AA Mutation | p.Arg449Ter(p.R449*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000335327 |
| Start | 26671917:26671917(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.468T>A |
| AA Mutation | p.Tyr156Ter(p.Y156*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000335327 |
| Start | 26681249:26681250(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | rs756173793 |
| CDS Mutation | c.920dupC |
| AA Mutation | p.Pro308AlafsTer29(p.P308Afs*29) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000335327 |
| Start | 26671936:26671937(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.493dupA |
| AA Mutation | p.Met165AsnfsTer27(p.M165Nfs*27) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000335327 |
| Start | 26685698:26685699(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.1367dupA |
| AA Mutation | p.Val457GlyfsTer17(p.V457Gfs*17) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | splice_acceptor_variant |
| Transcription ID | ENST00000335327 |
| Start | 26685687:26685687(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1352-1G>T |
| Mutation Classification | Splice_Site |
| Feature Type | Transcript |