Primary Site >> Stomach Cancer
Gene >> MED12
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000374080 |
| Start | 71124836:71124836(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2047G>C |
| AA Mutation | p.Asp683His(p.D683H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000374080 |
| Start | 71129408:71129408(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3670C>T |
| AA Mutation | p.Leu1224Phe(p.L1224F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000374080 |
| Start | 71126384:71126384(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2585G>A |
| AA Mutation | p.Gly862Asp(p.G862D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000374080 |
| Start | 71137226:71137226(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5591C>A |
| AA Mutation | p.Pro1864Gln(p.P1864Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000374080 |
| Start | 71136560:71136560(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5305A>C |
| AA Mutation | p.Thr1769Pro(p.T1769P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000374080 |
| Start | 71136420:71136420(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5165G>A |
| AA Mutation | p.Arg1722Gln(p.R1722Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000374080 |
| Start | 71127368:71127368(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs766598254 |
| CDS Mutation | c.2882G>A |
| AA Mutation | p.Arg961Gln(p.R961Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000374080 |
| Start | 71121120:71121120(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.703T>C |
| AA Mutation | p.Tyr235His(p.Y235H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000374080 |
| Start | 71129839:71129839(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3851G>A |
| AA Mutation | p.Arg1284His(p.R1284H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000374080 |
| Start | 71121391:71121391(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.800C>T |
| AA Mutation | p.Pro267Leu(p.P267L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000374080 |
| Start | 71121387:71121387(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.796C>T |
| AA Mutation | p.Arg266Cys(p.R266C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000374080 |
| Start | 71141928:71141928(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.6454G>A |
| AA Mutation | p.Ala2152Thr(p.A2152T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000374080 |
| Start | 71121599:71121599(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.884G>A |
| AA Mutation | p.Arg295His(p.R295H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000374080 |
| Start | 71128309:71128309(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3223G>A |
| AA Mutation | p.Ala1075Thr(p.A1075T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000374080 |
| Start | 71121756:71121756(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1041T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000374080 |
| Start | 71122582:71122582(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs371928861 |
| CDS Mutation | c.1323C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000374080 |
| Start | 71128624:71128624(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3381G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000374080 |
| Start | 71137332:71137332(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.5697G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000374080 |
| Start | 71129774:71129774(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3786G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000374080 |
| Start | 71136460:71136460(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs747836622 |
| CDS Mutation | c.5205C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |