Primary Site >> Stomach Cancer
Gene >> HSPA12A
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369209 |
| Start | 116681205:116681205(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.974T>G |
| AA Mutation | p.Val325Gly(p.V325G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000369209 |
| Start | 116676401:116676401(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1388T>C |
| AA Mutation | p.Leu463Pro(p.L463P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369209 |
| Start | 116675218:116675218(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs782645684 |
| CDS Mutation | c.1591C>T |
| AA Mutation | p.Arg531Cys(p.R531C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369209 |
| Start | 116700974:116700974(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.410A>C |
| AA Mutation | p.Glu137Ala(p.E137A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369209 |
| Start | 116692409:116692409(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200364186 |
| CDS Mutation | c.605C>T |
| AA Mutation | p.Thr202Met(p.T202M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369209 |
| Start | 116679623:116679623(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1166G>A |
| AA Mutation | p.Arg389His(p.R389H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369209 |
| Start | 116675217:116675217(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201237054 |
| CDS Mutation | c.1592G>A |
| AA Mutation | p.Arg531His(p.R531H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369209 |
| Start | 116679737:116679737(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1052T>C |
| AA Mutation | p.Val351Ala(p.V351A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369209 |
| Start | 116683808:116683808(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.818G>A |
| AA Mutation | p.Gly273Glu(p.G273E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369209 |
| Start | 116676420:116676420(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs199760082 |
| CDS Mutation | c.1369G>A |
| AA Mutation | p.Asp457Asn(p.D457N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369209 |
| Start | 116683882:116683882(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.744G>C |
| AA Mutation | p.Lys248Asn(p.K248N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369209 |
| Start | 116675302:116675302(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1507C>T |
| AA Mutation | p.Arg503Trp(p.R503W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369209 |
| Start | 116674894:116674894(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs375628817 |
| CDS Mutation | c.1915C>T |
| AA Mutation | p.Arg639Trp(p.R639W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369209 |
| Start | 116681859:116681859(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200867772 |
| CDS Mutation | c.854G>A |
| AA Mutation | p.Arg285His(p.R285H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369209 |
| Start | 116698666:116698666(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.515C>T |
| AA Mutation | p.Ala172Val(p.A172V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369209 |
| Start | 116676417:116676417(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1372A>G |
| AA Mutation | p.Ser458Gly(p.S458G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369209 |
| Start | 116675331:116675331(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs374696720 |
| CDS Mutation | c.1478C>T |
| AA Mutation | p.Ala493Val(p.A493V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369209 |
| Start | 116674936:116674936(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs575047261 |
| CDS Mutation | c.1873C>T |
| AA Mutation | p.Arg625Cys(p.R625C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000369209 |
| Start | 116675063:116675063(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1746G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000369209 |
| Start | 116675339:116675339(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1470G>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000369209 |
| Start | 116679589:116679589(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs782232321 |
| CDS Mutation | c.1200G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |