Primary Site >> Stomach Cancer
Gene >> TCERG1L
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368642 |
| Start | 131146569:131146569(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs192271138 |
| CDS Mutation | c.1126C>T |
| AA Mutation | p.Arg376Cys(p.R376C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368642 |
| Start | 131308370:131308370(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.511G>T |
| AA Mutation | p.Ala171Ser(p.A171S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368642 |
| Start | 131166864:131166864(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs769852465 |
| CDS Mutation | c.878G>A |
| AA Mutation | p.Arg293Gln(p.R293Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368642 |
| Start | 131093274:131093274(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs745519771 |
| CDS Mutation | c.1649G>T |
| AA Mutation | p.Arg550Met(p.R550M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368642 |
| Start | 131146527:131146527(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200282379 |
| CDS Mutation | c.1168C>T |
| AA Mutation | p.Arg390Cys(p.R390C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368642 |
| Start | 131146646:131146646(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs563448537 |
| CDS Mutation | c.1049C>T |
| AA Mutation | p.Thr350Met(p.T350M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368642 |
| Start | 131166817:131166817(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.925G>A |
| AA Mutation | p.Asp309Asn(p.D309N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368642 |
| Start | 131146538:131146538(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1157C>T |
| AA Mutation | p.Pro386Leu(p.P386L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368642 |
| Start | 131260391:131260391(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.724A>G |
| AA Mutation | p.Thr242Ala(p.T242A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000368642 |
| Start | 131309165:131309165(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.477T>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000368642 |
| Start | 131093312:131093312(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs373129269 |
| CDS Mutation | c.1611G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000368642 |
| Start | 131146645:131146645(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs763046074 |
| CDS Mutation | c.1050G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |