Primary Site >> Stomach Cancer
Gene >> LCT
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264162 |
| Start | 135804784:135804784(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs139591272 |
| CDS Mutation | c.4447G>A |
| AA Mutation | p.Ala1483Thr(p.A1483T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264162 |
| Start | 135836793:135836793(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.377A>G |
| AA Mutation | p.Gln126Arg(p.Q126R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264162 |
| Start | 135809619:135809619(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2728G>A |
| AA Mutation | p.Gly910Ser(p.G910S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264162 |
| Start | 135808920:135808920(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3427G>A |
| AA Mutation | p.Ala1143Thr(p.A1143T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264162 |
| Start | 135804115:135804115(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4478A>G |
| AA Mutation | p.His1493Arg(p.H1493R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264162 |
| Start | 135809123:135809123(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3224G>A |
| AA Mutation | p.Gly1075Asp(p.G1075D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264162 |
| Start | 135812446:135812446(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2218T>C |
| AA Mutation | p.Ser740Pro(p.S740P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264162 |
| Start | 135809355:135809355(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2992G>T |
| AA Mutation | p.Asp998Tyr(p.D998Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264162 |
| Start | 135809027:135809027(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3320C>T |
| AA Mutation | p.Thr1107Met(p.T1107M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264162 |
| Start | 135788452:135788452(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs376732886 |
| CDS Mutation | c.5656G>A |
| AA Mutation | p.Val1886Ile(p.V1886I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264162 |
| Start | 135809931:135809931(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2416G>A |
| AA Mutation | p.Glu806Lys(p.E806K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264162 |
| Start | 135817511:135817511(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1537G>A |
| AA Mutation | p.Glu513Lys(p.E513K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264162 |
| Start | 135790729:135790729(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5264G>A |
| AA Mutation | p.Arg1755Gln(p.R1755Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264162 |
| Start | 135836745:135836745(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs143420596 |
| CDS Mutation | c.425G>A |
| AA Mutation | p.Arg142Gln(p.R142Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264162 |
| Start | 135808774:135808774(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3573G>T |
| AA Mutation | p.Glu1191Asp(p.E1191D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264162 |
| Start | 135817829:135817829(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1219G>C |
| AA Mutation | p.Gly407Arg(p.G407R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264162 |
| Start | 135807264:135807264(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4037G>T |
| AA Mutation | p.Arg1346Leu(p.R1346L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264162 |
| Start | 135804125:135804125(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4468A>T |
| AA Mutation | p.Thr1490Ser(p.T1490S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264162 |
| Start | 135836746:135836746(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs760712703 |
| CDS Mutation | c.424C>T |
| AA Mutation | p.Arg142Trp(p.R142W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264162 |
| Start | 135823910:135823910(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.898C>A |
| AA Mutation | p.Leu300Ile(p.L300I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264162 |
| Start | 135809214:135809214(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3133T>C |
| AA Mutation | p.Tyr1045His(p.Y1045H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264162 |
| Start | 135809447:135809447(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2900G>A |
| AA Mutation | p.Arg967Gln(p.R967Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264162 |
| Start | 135800711:135800711(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs374357262 |
| CDS Mutation | c.4762G>A |
| AA Mutation | p.Ala1588Thr(p.A1588T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000264162 |
| Start | 135809068:135809068(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3279A>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 25 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000264162 |
| Start | 135804096:135804096(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4497G>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 26 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000264162 |
| Start | 135804866:135804866(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4365C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 27 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000264162 |
| Start | 135808531:135808531(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs375845174 |
| CDS Mutation | c.3816C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 28 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000264162 |
| Start | 135809587:135809587(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200579267 |
| CDS Mutation | c.2760C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 29 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000264162 |
| Start | 135789590:135789590(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs767789805 |
| CDS Mutation | c.5544C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 30 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000264162 |
| Start | 135809677:135809677(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2670A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 31 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000264162 |
| Start | 135809530:135809530(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2817A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 32 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000264162 |
| Start | 135809023:135809023(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs537926326 |
| CDS Mutation | c.3324C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 33 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000264162 |
| Start | 135790731:135790731(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5262G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 34 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000264162 |
| Start | 135809617:135809617(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs752135039 |
| CDS Mutation | c.2730C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 35 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000264162 |
| Start | 135809207:135809208(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.3139_3140delGA |
| AA Mutation | p.Asp1047LeufsTer8(p.D1047Lfs*8) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 36 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000264162 |
| Start | 135836708:135836709(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.461_462delAT |
| AA Mutation | p.Tyr154CysfsTer20(p.Y154Cfs*20) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 37 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000264162 |
| Start | 135788362:135788362(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs369141275 |
| CDS Mutation | c.5746C>T |
| AA Mutation | p.Arg1916Ter(p.R1916*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 38 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000264162 |
| Start | 135817595:135817595(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs779838486 |
| CDS Mutation | c.1453C>T |
| AA Mutation | p.Gln485Ter(p.Q485*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |