Primary Site >> Stomach Cancer
Gene >> HSPH1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000320027 |
| Start | 31155627:31155627(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.193T>A |
| AA Mutation | p.Ser65Thr(p.S65T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000320027 |
| Start | 31138516:31138516(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2261C>A |
| AA Mutation | p.Ser754Tyr(p.S754Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000320027 |
| Start | 31137518:31137518(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2377A>G |
| AA Mutation | p.Asn793Asp(p.N793D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000320027 |
| Start | 31141186:31141186(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1790C>T |
| AA Mutation | p.Pro597Leu(p.P597L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000320027 |
| Start | 31145694:31145694(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1453A>G |
| AA Mutation | p.Asn485Asp(p.N485D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000320027 |
| Start | 31137487:31137487(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2408C>T |
| AA Mutation | p.Pro803Leu(p.P803L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000320027 |
| Start | 31158817:31158817(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.154G>A |
| AA Mutation | p.Ala52Thr(p.A52T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000320027 |
| Start | 31139062:31139062(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs527818681 |
| CDS Mutation | c.2026C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000320027 |
| Start | 31150961:31150961(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs749589942 |
| CDS Mutation | c.894C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000320027 |
| Start | 31150050:31150050(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1041T>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000320027 |
| Start | 31143867:31143867(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1641T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000320027 |
| Start | 31151654:31151654(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.618A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000320027 |
| Start | 31143861:31143861(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs752487587 |
| CDS Mutation | c.1647A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000320027 |
| Start | 31141190:31141190(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1786C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000320027 |
| Start | 31155553:31155553(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs575501640 |
| CDS Mutation | c.267C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |