Primary Site >> Stomach Cancer
Gene >> SLIT3
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000519560 |
| Start | 168772790:168772790(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs372219038 |
| CDS Mutation | c.1450C>T |
| AA Mutation | p.Arg484Cys(p.R484C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000519560 |
| Start | 169244762:169244762(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.284A>G |
| AA Mutation | p.Asn95Ser(p.N95S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000519560 |
| Start | 168817393:168817393(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs755004583 |
| CDS Mutation | c.700C>T |
| AA Mutation | p.Arg234Trp(p.R234W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000519560 |
| Start | 168817354:168817354(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs761268448 |
| CDS Mutation | c.739C>T |
| AA Mutation | p.His247Tyr(p.H247Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000519560 |
| Start | 168722980:168722980(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2364C>A |
| AA Mutation | p.Ser788Arg(p.S788R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000519560 |
| Start | 168669898:168669898(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4221C>G |
| AA Mutation | p.Asp1407Glu(p.D1407E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000519560 |
| Start | 168669793:168669793(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4326C>G |
| AA Mutation | p.His1442Gln(p.H1442Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000519560 |
| Start | 168806464:168806464(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.917C>T |
| AA Mutation | p.Pro306Leu(p.P306L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000519560 |
| Start | 168708004:168708004(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2816A>G |
| AA Mutation | p.Tyr939Cys(p.Y939C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000519560 |
| Start | 168753903:168753903(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1790A>G |
| AA Mutation | p.His597Arg(p.H597R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000519560 |
| Start | 168760925:168760925(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1622A>G |
| AA Mutation | p.Asp541Gly(p.D541G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000519560 |
| Start | 168722939:168722939(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2405C>T |
| AA Mutation | p.Ser802Phe(p.S802F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000519560 |
| Start | 168666618:168666618(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4408G>T |
| AA Mutation | p.Ala1470Ser(p.A1470S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000519560 |
| Start | 168772814:168772814(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1426A>G |
| AA Mutation | p.Ser476Gly(p.S476G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000519560 |
| Start | 168722272:168722272(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs199918063 |
| CDS Mutation | c.2467C>T |
| AA Mutation | p.Arg823Trp(p.R823W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000519560 |
| Start | 168696405:168696405(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2969G>T |
| AA Mutation | p.Gly990Val(p.G990V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000519560 |
| Start | 168671375:168671375(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3950A>G |
| AA Mutation | p.Asp1317Gly(p.D1317G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000519560 |
| Start | 168749492:168749492(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2117T>G |
| AA Mutation | p.Ile706Ser(p.I706S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000519560 |
| Start | 168666683:168666683(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs755657006 |
| CDS Mutation | c.4343C>T |
| AA Mutation | p.Pro1448Leu(p.P1448L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000519560 |
| Start | 168774351:168774351(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1179C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000519560 |
| Start | 168669817:168669817(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4302C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000519560 |
| Start | 168806535:168806535(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs745827589 |
| CDS Mutation | c.846G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000519560 |
| Start | 168748340:168748340(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs779092935 |
| CDS Mutation | c.2232C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000519560 |
| Start | 168748422:168748426(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.2146_2150delGAGAG |
| AA Mutation | p.Glu716Ter(p.E716*) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 25 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000519560 |
| Start | 168817436:168817436(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.657C>A |
| AA Mutation | p.Cys219Ter(p.C219*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 26 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000519560 |
| Start | 168817396:168817396(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs757311008 |
| CDS Mutation | c.697C>T |
| AA Mutation | p.Arg233Ter(p.R233*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 27 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000519560 |
| Start | 168666663:168666663(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4363C>T |
| AA Mutation | p.Arg1455Ter(p.R1455*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |