Primary Site >> Stomach Cancer
Gene >> DLEC1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000308059 |
| Start | 38121730:38121730(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4969G>A |
| AA Mutation | p.Val1657Ile(p.V1657I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000308059 |
| Start | 38122392:38122392(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5248A>G |
| AA Mutation | p.Met1750Val(p.M1750V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000308059 |
| Start | 38108411:38108411(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs372104796 |
| CDS Mutation | c.3025G>A |
| AA Mutation | p.Gly1009Arg(p.G1009R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000308059 |
| Start | 38097887:38097887(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2709G>T |
| AA Mutation | p.Gln903His(p.Q903H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000308059 |
| Start | 38059822:38059822(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs149190717 |
| CDS Mutation | c.643G>A |
| AA Mutation | p.Asp215Asn(p.D215N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000308059 |
| Start | 38039297:38039297(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs750125618 |
| CDS Mutation | c.72G>C |
| AA Mutation | p.Trp24Cys(p.W24C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000308059 |
| Start | 38088296:38088296(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1573G>A |
| AA Mutation | p.Ala525Thr(p.A525T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000308059 |
| Start | 38117254:38117254(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs750378238 |
| CDS Mutation | c.4352C>T |
| AA Mutation | p.Ala1451Val(p.A1451V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000308059 |
| Start | 38121719:38121719(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs573428697 |
| CDS Mutation | c.4958G>A |
| AA Mutation | p.Arg1653Gln(p.R1653Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000308059 |
| Start | 38039377:38039377(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs181606392 |
| CDS Mutation | c.152A>G |
| AA Mutation | p.Tyr51Cys(p.Y51C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000308059 |
| Start | 38112225:38112225(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3530T>C |
| AA Mutation | p.Met1177Thr(p.M1177T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000308059 |
| Start | 38117879:38117879(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4559T>C |
| AA Mutation | p.Leu1520Pro(p.L1520P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000308059 |
| Start | 38096642:38096642(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2245G>T |
| AA Mutation | p.Gly749Cys(p.G749C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000308059 |
| Start | 38096679:38096679(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2282A>T |
| AA Mutation | p.Tyr761Phe(p.Y761F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000308059 |
| Start | 38039334:38039334(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.109A>G |
| AA Mutation | p.Ser37Gly(p.S37G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000308059 |
| Start | 38097765:38097765(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs746750302 |
| CDS Mutation | c.2587G>A |
| AA Mutation | p.Val863Ile(p.V863I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000308059 |
| Start | 38114408:38114408(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3733C>A |
| AA Mutation | p.Leu1245Met(p.L1245M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000308059 |
| Start | 38086265:38086265(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1460A>G |
| AA Mutation | p.Tyr487Cys(p.Y487C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000308059 |
| Start | 38117870:38117870(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4550A>G |
| AA Mutation | p.Tyr1517Cys(p.Y1517C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000308059 |
| Start | 38094992:38094992(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2033C>T |
| AA Mutation | p.Ala678Val(p.A678V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000308059 |
| Start | 38084187:38084187(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1203G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000308059 |
| Start | 38117288:38117288(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4386C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000308059 |
| Start | 38107686:38107686(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2967C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000308059 |
| Start | 38117228:38117228(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4326G>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 25 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000308059 |
| Start | 38062688:38062688(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.986delA |
| AA Mutation | p.Asn329IlefsTer26(p.N329Ifs*26) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 26 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000308059 |
| Start | 38062700:38062700(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.999delT |
| AA Mutation | p.Pro334LeufsTer21(p.P334Lfs*21) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 27 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000308059 |
| Start | 38084203:38084203(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs377205155 |
| CDS Mutation | c.1219C>T |
| AA Mutation | p.Arg407Ter(p.R407*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 28 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000308059 |
| Start | 38121715:38121715(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs772223976 |
| CDS Mutation | c.4954C>T |
| AA Mutation | p.Gln1652Ter(p.Q1652*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 29 |
| Mutation Consequence | splice_acceptor_variant |
| Transcription ID | ENST00000308059 |
| Start | 38084156:38084156(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1174-2A>G |
| Mutation Classification | Splice_Site |
| Feature Type | Transcript |