Primary Site >> Stomach Cancer
Gene >> PLCG2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000564138 |
| Start | 81936357:81936357(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3031G>A |
| AA Mutation | p.Ala1011Thr(p.A1011T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000564138 |
| Start | 81931519:81931519(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2604C>A |
| AA Mutation | p.Asn868Lys(p.N868K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000564138 |
| Start | 81956795:81956795(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs370547009 |
| CDS Mutation | c.3671G>A |
| AA Mutation | p.Arg1224His(p.R1224H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000564138 |
| Start | 81889225:81889225(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.819T>G |
| AA Mutation | p.Ile273Met(p.I273M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000564138 |
| Start | 81900687:81900687(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1269A>C |
| AA Mutation | p.Glu423Asp(p.E423D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000564138 |
| Start | 81910579:81910579(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1793A>C |
| AA Mutation | p.Lys598Thr(p.K598T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000564138 |
| Start | 81919641:81919641(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2212G>A |
| AA Mutation | p.Glu738Lys(p.E738K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000564138 |
| Start | 81910668:81910668(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1882G>A |
| AA Mutation | p.Glu628Lys(p.E628K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000564138 |
| Start | 81858305:81858305(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.380A>G |
| AA Mutation | p.Lys127Arg(p.K127R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000564138 |
| Start | 81919558:81919558(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2129T>C |
| AA Mutation | p.Phe710Ser(p.F710S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000564138 |
| Start | 81928610:81928610(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2567A>C |
| AA Mutation | p.Asn856Thr(p.N856T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000564138 |
| Start | 81910639:81910639(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs769887285 |
| CDS Mutation | c.1853G>A |
| AA Mutation | p.Arg618His(p.R618H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000564138 |
| Start | 81931654:81931654(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2739G>T |
| AA Mutation | p.Lys913Asn(p.K913N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000564138 |
| Start | 81786123:81786123(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.134T>C |
| AA Mutation | p.Val45Ala(p.V45A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000564138 |
| Start | 81883319:81883319(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.743G>A |
| AA Mutation | p.Arg248Lys(p.R248K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000564138 |
| Start | 81936373:81936373(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs755551138 |
| CDS Mutation | c.3047C>T |
| AA Mutation | p.Thr1016Met(p.T1016M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000564138 |
| Start | 81895823:81895823(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1089G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000564138 |
| Start | 81895838:81895838(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs769107090 |
| CDS Mutation | c.1104G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000564138 |
| Start | 81891525:81891525(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs533700490 |
| CDS Mutation | c.921C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000564138 |
| Start | 81893742:81893742(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs778079439 |
| CDS Mutation | c.1020G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000564138 |
| Start | 81910640:81910640(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1854C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000564138 |
| Start | 81912660:81912660(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs745784908 |
| CDS Mutation | c.1998C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000564138 |
| Start | 81900747:81900747(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs369281824 |
| CDS Mutation | c.1329G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000564138 |
| Start | 81910568:81910568(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs752950221 |
| CDS Mutation | c.1782C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 25 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000564138 |
| Start | 81889179:81889179(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.773G>A |
| AA Mutation | p.Trp258Ter(p.W258*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 26 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000564138 |
| Start | 81908519:81908520(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.1667dupG |
| AA Mutation | p.Lys557GlnfsTer16(p.K557Qfs*16) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |