Primary Site >> Stomach Cancer
Gene >> MLH3
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000355774 |
| Start | 75046633:75046633(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs770819541 |
| CDS Mutation | c.3023C>T |
| AA Mutation | p.Pro1008Leu(p.P1008L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000355774 |
| Start | 75047212:75047212(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs757328325 |
| CDS Mutation | c.2444A>G |
| AA Mutation | p.Asp815Gly(p.D815G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000355774 |
| Start | 75049615:75049615(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs760072474 |
| CDS Mutation | c.41G>A |
| AA Mutation | p.Arg14His(p.R14H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000355774 |
| Start | 75046904:75046904(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs762167939 |
| CDS Mutation | c.2752G>T |
| AA Mutation | p.Asp918Tyr(p.D918Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000355774 |
| Start | 75038343:75038343(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3640G>A |
| AA Mutation | p.Ala1214Thr(p.A1214T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000355774 |
| Start | 75048514:75048514(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs751375245 |
| CDS Mutation | c.1142G>A |
| AA Mutation | p.Arg381His(p.R381H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000355774 |
| Start | 75047008:75047008(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2648C>T |
| AA Mutation | p.Ser883Phe(p.S883F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000355774 |
| Start | 75049232:75049232(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs745639930 |
| CDS Mutation | c.424G>A |
| AA Mutation | p.Ala142Thr(p.A142T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000355774 |
| Start | 75046545:75046545(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3111A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000355774 |
| Start | 75047220:75047220(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2436T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000355774 |
| Start | 75018952:75018952(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4119C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000355774 |
| Start | 75047982:75047982(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1674T>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000355774 |
| Start | 75047901:75047901(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs766244000 |
| CDS Mutation | c.1755delA |
| AA Mutation | p.Glu586AsnfsTer24(p.E586Nfs*24) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |