Primary Site >> Stomach Cancer
Gene >> MEN1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000337652 |
| Start | 64805132:64805132(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1267G>T |
| AA Mutation | p.Asp423Tyr(p.D423Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000337652 |
| Start | 64806293:64806293(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1003C>T |
| AA Mutation | p.Arg335Cys(p.R335C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000337652 |
| Start | 64805165:64805165(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1234C>A |
| AA Mutation | p.Pro412Thr(p.P412T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000337652 |
| Start | 64807625:64807625(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs760289964 |
| CDS Mutation | c.725C>T |
| AA Mutation | p.Ala242Val(p.A242V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000337652 |
| Start | 64808009:64808009(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.551A>G |
| AA Mutation | p.Glu184Gly(p.E184G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000337652 |
| Start | 64804772:64804772(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs748820252 |
| CDS Mutation | c.1410C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000337652 |
| Start | 64804757:64804757(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1425G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000337652 |
| Start | 64805646:64805646(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1189delG |
| AA Mutation | p.Glu397SerfsTer53(p.E397Sfs*53) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000337652 |
| Start | 64804621:64804621(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs794728642 |
| CDS Mutation | c.1561delC |
| AA Mutation | p.Arg521GlyfsTer43(p.R521Gfs*43) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |