Primary Site >> Stomach Cancer
Gene >> HYAL1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000266031 |
| Start | 50302376:50302376(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs782692817 |
| CDS Mutation | c.581G>A |
| AA Mutation | p.Arg194His(p.R194H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000266031 |
| Start | 50300679:50300679(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs587595632 |
| CDS Mutation | c.1112G>A |
| AA Mutation | p.Arg371His(p.R371H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000266031 |
| Start | 50302418:50302418(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs782751421 |
| CDS Mutation | c.539G>A |
| AA Mutation | p.Arg180Gln(p.R180Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000266031 |
| Start | 50302830:50302830(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.127T>C |
| AA Mutation | p.Cys43Arg(p.C43R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000266031 |
| Start | 50302766:50302766(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.191A>T |
| AA Mutation | p.Gln64Leu(p.Q64L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000266031 |
| Start | 50302610:50302610(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.347C>T |
| AA Mutation | p.Ala116Val(p.A116V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000266031 |
| Start | 50302146:50302146(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs782752459 |
| CDS Mutation | c.811C>T |
| AA Mutation | p.Arg271Cys(p.R271C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000266031 |
| Start | 50302745:50302745(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.212T>A |
| AA Mutation | p.Met71Lys(p.M71K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000266031 |
| Start | 50302277:50302277(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.680C>T |
| AA Mutation | p.Ala227Val(p.A227V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000266031 |
| Start | 50300632:50300632(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1159T>C |
| AA Mutation | p.Phe387Leu(p.F387L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000266031 |
| Start | 50302930:50302930(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs781916060 |
| CDS Mutation | c.27C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000266031 |
| Start | 50302765:50302765(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.192delG |
| AA Mutation | p.Thr65ProfsTer7(p.T65Pfs*7) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |