Primary Site >> Stomach Cancer
Gene >> WISP1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000250160 |
| Start | 133220680:133220680(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201971205 |
| CDS Mutation | c.449C>T |
| AA Mutation | p.Ala150Val(p.A150V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000250160 |
| Start | 133212961:133212961(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.167C>T |
| AA Mutation | p.Pro56Leu(p.P56L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000250160 |
| Start | 133220616:133220616(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs199909788 |
| CDS Mutation | c.385C>T |
| AA Mutation | p.Arg129Cys(p.R129C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000250160 |
| Start | 133220824:133220824(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs34782842 |
| CDS Mutation | c.593G>A |
| AA Mutation | p.Arg198His(p.R198H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000250160 |
| Start | 133220835:133220835(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.604G>A |
| AA Mutation | p.Ala202Thr(p.A202T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000250160 |
| Start | 133212927:133212927(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs529938783 |
| CDS Mutation | c.133C>T |
| AA Mutation | p.Arg45Cys(p.R45C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000250160 |
| Start | 133227564:133227564(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs764654100 |
| CDS Mutation | c.958G>A |
| AA Mutation | p.Val320Met(p.V320M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000250160 |
| Start | 133212928:133212928(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs753495859 |
| CDS Mutation | c.134G>A |
| AA Mutation | p.Arg45His(p.R45H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000250160 |
| Start | 133220655:133220655(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.424T>C |
| AA Mutation | p.Tyr142His(p.Y142H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000250160 |
| Start | 133220841:133220841(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs760709240 |
| CDS Mutation | c.610G>A |
| AA Mutation | p.Asp204Asn(p.D204N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000250160 |
| Start | 133220742:133220742(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs140971140 |
| CDS Mutation | c.511C>T |
| AA Mutation | p.Arg171Trp(p.R171W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000250160 |
| Start | 133227487:133227487(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.881G>A |
| AA Mutation | p.Arg294His(p.R294H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000250160 |
| Start | 133225572:133225572(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.793A>G |
| AA Mutation | p.Thr265Ala(p.T265A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000250160 |
| Start | 133220740:133220740(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs139058011 |
| CDS Mutation | c.509C>T |
| AA Mutation | p.Pro170Leu(p.P170L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000250160 |
| Start | 133213115:133213115(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.321C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000250160 |
| Start | 133213058:133213058(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.264G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000250160 |
| Start | 133212959:133212959(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.165C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000250160 |
| Start | 133220675:133220675(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs755626224 |
| CDS Mutation | c.444C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000250160 |
| Start | 133225418:133225418(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.639C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000250160 |
| Start | 133227563:133227563(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs758449163 |
| CDS Mutation | c.957C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000250160 |
| Start | 133220672:133220672(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs759412122 |
| CDS Mutation | c.441C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000250160 |
| Start | 133191201:133191201(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.57C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000250160 |
| Start | 133220720:133220720(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs368562535 |
| CDS Mutation | c.489G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000250160 |
| Start | 133220627:133220627(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.396C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 25 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000250160 |
| Start | 133213031:133213031(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs752374588 |
| CDS Mutation | c.237C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 26 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000250160 |
| Start | 133220747:133220747(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs150221105 |
| CDS Mutation | c.516C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 27 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000250160 |
| Start | 133220678:133220678(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs530441446 |
| CDS Mutation | c.447C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 28 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000250160 |
| Start | 133225475:133225475(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.700delG |
| AA Mutation | p.Val234SerfsTer50(p.V234Sfs*50) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 29 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000250160 |
| Start | 133220714:133220714(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.488delC |
| AA Mutation | p.Pro163ArgfsTer11(p.P163Rfs*11) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 30 |
| Mutation Consequence | stop_gained;splice_region_variant |
| Transcription ID | ENST00000250160 |
| Start | 133213143:133213143(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.349C>T |
| AA Mutation | p.Gln117Ter(p.Q117*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 31 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000250160 |
| Start | 133220713:133220714(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | rs773550125 |
| CDS Mutation | c.488dupC |
| AA Mutation | p.Arg164AlafsTer18(p.R164Afs*18) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |