Primary Site >> Stomach Cancer
Gene >> LZTS1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265801 |
| Start | 20254890:20254890(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.292T>A |
| AA Mutation | p.Phe98Ile(p.F98I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265801 |
| Start | 20253333:20253333(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs762386540 |
| CDS Mutation | c.598G>A |
| AA Mutation | p.Val200Met(p.V200M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265801 |
| Start | 20253045:20253045(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs779973869 |
| CDS Mutation | c.886G>A |
| AA Mutation | p.Glu296Lys(p.E296K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265801 |
| Start | 20250078:20250078(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1435C>T |
| AA Mutation | p.Arg479Trp(p.R479W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265801 |
| Start | 20255154:20255154(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs770015908 |
| CDS Mutation | c.28G>A |
| AA Mutation | p.Gly10Ser(p.G10S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265801 |
| Start | 20249847:20249847(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs748585946 |
| CDS Mutation | c.1666C>T |
| AA Mutation | p.Arg556Trp(p.R556W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265801 |
| Start | 20250009:20250009(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1504C>T |
| AA Mutation | p.Arg502Trp(p.R502W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265801 |
| Start | 20254890:20254890(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.292T>G |
| AA Mutation | p.Phe98Val(p.F98V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265801 |
| Start | 20253483:20253483(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.448C>T |
| AA Mutation | p.His150Tyr(p.H150Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265801 |
| Start | 20249906:20249906(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1607A>C |
| AA Mutation | p.Lys536Thr(p.K536T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265801 |
| Start | 20253156:20253156(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.775G>T |
| AA Mutation | p.Asp259Tyr(p.D259Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265801 |
| Start | 20250057:20250057(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs772213928 |
| CDS Mutation | c.1456C>T |
| AA Mutation | p.Arg486Cys(p.R486C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000265801 |
| Start | 20253142:20253142(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.789C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000265801 |
| Start | 20253421:20253421(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs569968765 |
| CDS Mutation | c.510G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000265801 |
| Start | 20253205:20253205(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs141673059 |
| CDS Mutation | c.726G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000265801 |
| Start | 20252950:20252950(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs747506414 |
| CDS Mutation | c.981G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000265801 |
| Start | 20253334:20253334(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.597C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000265801 |
| Start | 20250237:20250237(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1276C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000265801 |
| Start | 20252989:20252989(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.942C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000265801 |
| Start | 20250199:20250199(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs758448126 |
| CDS Mutation | c.1314C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000265801 |
| Start | 20254929:20254929(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.253C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000265801 |
| Start | 20253229:20253229(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs146205759 |
| CDS Mutation | c.702C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000265801 |
| Start | 20255026:20255026(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs745621744 |
| CDS Mutation | c.156C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000265801 |
| Start | 20253166:20253166(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.765delC |
| AA Mutation | p.Ile256SerfsTer98(p.I256Sfs*98) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |