Primary Site >> Stomach Cancer
Gene >> LAMA4
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000230538 |
| Start | 112109565:112109565(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs145897390 |
| CDS Mutation | c.5344C>T |
| AA Mutation | p.Arg1782Cys(p.R1782C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000230538 |
| Start | 112139253:112139253(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3149A>G |
| AA Mutation | p.Tyr1050Cys(p.Y1050C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000230538 |
| Start | 112120339:112120339(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4609C>T |
| AA Mutation | p.His1537Tyr(p.H1537Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000230538 |
| Start | 112175438:112175438(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1232T>G |
| AA Mutation | p.Leu411Arg(p.L411R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000230538 |
| Start | 112191687:112191687(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs372074151 |
| CDS Mutation | c.667C>T |
| AA Mutation | p.Arg223Cys(p.R223C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000230538 |
| Start | 112175321:112175321(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1349C>T |
| AA Mutation | p.Ala450Val(p.A450V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000230538 |
| Start | 112165160:112165160(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1668G>C |
| AA Mutation | p.Lys556Asn(p.K556N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000230538 |
| Start | 112133470:112133470(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3575T>G |
| AA Mutation | p.Leu1192Arg(p.L1192R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000230538 |
| Start | 112134510:112134510(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3514G>T |
| AA Mutation | p.Asp1172Tyr(p.D1172Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000230538 |
| Start | 112165171:112165171(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1657G>C |
| AA Mutation | p.Asp553His(p.D553H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000230538 |
| Start | 112139272:112139272(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3130C>A |
| AA Mutation | p.Gln1044Lys(p.Q1044K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000230538 |
| Start | 112139181:112139181(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs782099866 |
| CDS Mutation | c.3221G>A |
| AA Mutation | p.Arg1074His(p.R1074H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000230538 |
| Start | 112120321:112120321(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4627A>G |
| AA Mutation | p.Arg1543Gly(p.R1543G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000230538 |
| Start | 112191705:112191705(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.649A>G |
| AA Mutation | p.Thr217Ala(p.T217A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000230538 |
| Start | 112122144:112122144(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs372872387 |
| CDS Mutation | c.4345C>T |
| AA Mutation | p.Arg1449Trp(p.R1449W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000230538 |
| Start | 112191752:112191752(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.602A>G |
| AA Mutation | p.Asp201Gly(p.D201G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000230538 |
| Start | 112207136:112207136(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs138176093 |
| CDS Mutation | c.307C>T |
| AA Mutation | p.Arg103Trp(p.R103W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000230538 |
| Start | 112178156:112178156(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1154T>C |
| AA Mutation | p.Val385Ala(p.V385A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000230538 |
| Start | 112172663:112172663(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1499G>T |
| AA Mutation | p.Arg500Met(p.R500M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000230538 |
| Start | 112140848:112140848(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2888A>G |
| AA Mutation | p.Lys963Arg(p.K963R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000230538 |
| Start | 112187493:112187493(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.923A>G |
| AA Mutation | p.His308Arg(p.H308R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000230538 |
| Start | 112133477:112133477(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3568G>T |
| AA Mutation | p.Ala1190Ser(p.A1190S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000230538 |
| Start | 112172622:112172622(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs782767592 |
| CDS Mutation | c.1540C>T |
| AA Mutation | p.Arg514Trp(p.R514W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000230538 |
| Start | 112139762:112139762(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3100C>T |
| AA Mutation | p.Pro1034Ser(p.P1034S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 25 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000230538 |
| Start | 112109473:112109473(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs782692429 |
| CDS Mutation | c.5436C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 26 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000230538 |
| Start | 112191808:112191808(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.546C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 27 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000230538 |
| Start | 112117887:112117887(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4833C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 28 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000230538 |
| Start | 112142266:112142266(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2520C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 29 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000230538 |
| Start | 112150608:112150608(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2076T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 30 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000230538 |
| Start | 112187561:112187561(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.855G>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 31 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000230538 |
| Start | 112131069:112131069(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3867T>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 32 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000230538 |
| Start | 112187588:112187588(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs782380339 |
| CDS Mutation | c.828C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 33 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000230538 |
| Start | 112140896:112140896(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.2840delT |
| AA Mutation | p.Leu947Ter(p.L947*) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 34 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000230538 |
| Start | 112128964:112128964(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.4245delA |
| AA Mutation | p.Gly1416GlufsTer29(p.G1416Efs*29) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 35 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000230538 |
| Start | 112117787:112117788(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.4932dupC |
| AA Mutation | p.Met1645HisfsTer18(p.M1645Hfs*18) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |
| ID | 36 |
| Mutation Consequence | splice_donor_variant |
| Transcription ID | ENST00000230538 |
| Start | 112175312:112175312(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1357+1G>A |
| Mutation Classification | Splice_Site |
| Feature Type | Transcript |
| ID | 37 |
| Mutation Consequence | protein_altering_variant |
| Transcription ID | ENST00000230538 |
| Start | 112158822:112158823(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.1726_1727insCAACCAACA |
| AA Mutation | p.Leu576delinsProThrAsnIle(p.L576delinsPTNI) |
| Mutation Classification | In_Frame_Ins |
| Feature Type | Transcript |