Primary Site >> Stomach Cancer
Gene >> MMP28
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000605424 |
| Start | 35766621:35766621(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1442G>A |
| AA Mutation | p.Arg481Gln(p.R481Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000605424 |
| Start | 35773300:35773300(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.484T>C |
| AA Mutation | p.Trp162Arg(p.W162R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000605424 |
| Start | 35778992:35778992(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.275G>T |
| AA Mutation | p.Gly92Val(p.G92V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000605424 |
| Start | 35779023:35779023(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.244A>G |
| AA Mutation | p.Thr82Ala(p.T82A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000605424 |
| Start | 35767847:35767847(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1073A>T |
| AA Mutation | p.Glu358Val(p.E358V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000605424 |
| Start | 35770232:35770232(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.685C>T |
| AA Mutation | p.Arg229Cys(p.R229C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000605424 |
| Start | 35766708:35766708(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1355A>G |
| AA Mutation | p.Tyr452Cys(p.Y452C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000605424 |
| Start | 35779028:35779028(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs531148530 |
| CDS Mutation | c.239G>A |
| AA Mutation | p.Arg80His(p.R80H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000605424 |
| Start | 35779039:35779039(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.228C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000605424 |
| Start | 35778985:35778985(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.282A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000605424 |
| Start | 35779043:35779044(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.223dupA |
| AA Mutation | p.Ser75LysfsTer30(p.S75Kfs*30) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | inframe_deletion |
| Transcription ID | ENST00000605424 |
| Start | 35773268:35773276(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.508_516delTTCTGGGAG |
| AA Mutation | p.Phe170_Glu172del(p.F170_E172del) |
| Mutation Classification | In_Frame_Del |
| Feature Type | Transcript |