Primary Site >> Stomach Cancer
Gene >> HSPA1A
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000375651 |
| Start | 31817475:31817475(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1719G>T |
| AA Mutation | p.Lys573Asn(p.K573N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000375651 |
| Start | 31817518:31817518(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs777027010 |
| CDS Mutation | c.1762G>A |
| AA Mutation | p.Glu588Lys(p.E588K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000375651 |
| Start | 31815866:31815866(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.110C>T |
| AA Mutation | p.Thr37Ile(p.T37I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000375651 |
| Start | 31815766:31815766(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.10G>T |
| AA Mutation | p.Ala4Ser(p.A4S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000375651 |
| Start | 31817623:31817623(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1867G>T |
| AA Mutation | p.Gly623Trp(p.G623W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000375651 |
| Start | 31817579:31817579(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1823G>A |
| AA Mutation | p.Ser608Asn(p.S608N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000375651 |
| Start | 31815792:31815792(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs774374754 |
| CDS Mutation | c.36C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |