Primary Site >> Stomach Cancer
Gene >> L1CAM
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000370060 |
| Start | 153865751:153865751(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs782716607 |
| CDS Mutation | c.2500C>T |
| AA Mutation | p.Arg834Trp(p.R834W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000370060 |
| Start | 153872155:153872155(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.397G>A |
| AA Mutation | p.Glu133Lys(p.E133K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000370060 |
| Start | 153863546:153863546(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3461A>C |
| AA Mutation | p.Lys1154Thr(p.K1154T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000370060 |
| Start | 153864417:153864417(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs781826722 |
| CDS Mutation | c.3227C>T |
| AA Mutation | p.Thr1076Met(p.T1076M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000370060 |
| Start | 153868345:153868345(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1660C>T |
| AA Mutation | p.Arg554Cys(p.R554C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000370060 |
| Start | 153864355:153864355(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs782807254 |
| CDS Mutation | c.3289C>T |
| AA Mutation | p.Arg1097Trp(p.R1097W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000370060 |
| Start | 153868040:153868040(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs137940405 |
| CDS Mutation | c.1786G>A |
| AA Mutation | p.Glu596Lys(p.E596K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000370060 |
| Start | 153868866:153868866(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs137852520 |
| CDS Mutation | c.1354G>A |
| AA Mutation | p.Gly452Arg(p.G452R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000370060 |
| Start | 153866736:153866736(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200385894 |
| CDS Mutation | c.2344G>A |
| AA Mutation | p.Val782Met(p.V782M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000370060 |
| Start | 153868905:153868905(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1315G>A |
| AA Mutation | p.Val439Ile(p.V439I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000370060 |
| Start | 153868627:153868627(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs782155168 |
| CDS Mutation | c.1480C>T |
| AA Mutation | p.Arg494Cys(p.R494C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000370060 |
| Start | 153864923:153864923(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2944G>A |
| AA Mutation | p.Asp982Asn(p.D982N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000370060 |
| Start | 153869630:153869630(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201882430 |
| CDS Mutation | c.1157G>A |
| AA Mutation | p.Arg386His(p.R386H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000370060 |
| Start | 153870473:153870473(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201642622 |
| CDS Mutation | c.721C>T |
| AA Mutation | p.Arg241Cys(p.R241C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000370060 |
| Start | 153863485:153863485(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3522C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000370060 |
| Start | 153865197:153865197(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs781813303 |
| CDS Mutation | c.2763C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000370060 |
| Start | 153862822:153862822(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs782110886 |
| CDS Mutation | c.3615C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000370060 |
| Start | 153868436:153868436(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1569G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000370060 |
| Start | 153870881:153870881(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs782223025 |
| CDS Mutation | c.603C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000370060 |
| Start | 153864452:153864452(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3192G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000370060 |
| Start | 153867471:153867471(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2022T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000370060 |
| Start | 153872165:153872165(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.387G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000370060 |
| Start | 153862762:153862762(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201625971 |
| CDS Mutation | c.3675C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000370060 |
| Start | 153862825:153862825(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3612T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 25 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000370060 |
| Start | 153870138:153870138(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.909C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 26 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000370060 |
| Start | 153869596:153869596(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1191T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 27 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000370060 |
| Start | 153866841:153866841(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs782198738 |
| CDS Mutation | c.2239delC |
| AA Mutation | p.Gln747ArgfsTer104(p.Q747Rfs*104) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 28 |
| Mutation Consequence | inframe_deletion |
| Transcription ID | ENST00000370060 |
| Start | 153865135:153865137(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.2823_2825delACT |
| AA Mutation | p.Leu942del(p.L942del) |
| Mutation Classification | In_Frame_Del |
| Feature Type | Transcript |