Primary Site >> Stomach Cancer
Gene >> CALD1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000361675 |
| Start | 134933554:134933554(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.785A>C |
| AA Mutation | p.Lys262Thr(p.K262T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000361675 |
| Start | 134867744:134867744(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.11T>G |
| AA Mutation | p.Phe4Cys(p.F4C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000361675 |
| Start | 134928806:134928806(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.124C>T |
| AA Mutation | p.Arg42Cys(p.R42C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000361675 |
| Start | 134933336:134933336(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.567A>C |
| AA Mutation | p.Glu189Asp(p.E189D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000361675 |
| Start | 134933088:134933088(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs775853439 |
| CDS Mutation | c.319C>T |
| AA Mutation | p.Arg107Cys(p.R107C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000361675 |
| Start | 134933283:134933283(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.514T>C |
| AA Mutation | p.Tyr172His(p.Y172H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000361675 |
| Start | 134958251:134958251(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2022G>T |
| AA Mutation | p.Lys674Asn(p.K674N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000361675 |
| Start | 134867750:134867750(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs772216381 |
| CDS Mutation | c.17G>A |
| AA Mutation | p.Arg6His(p.R6H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000361675 |
| Start | 134947602:134947602(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1627C>T |
| AA Mutation | p.Arg543Cys(p.R543C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000361675 |
| Start | 134947657:134947657(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs769729218 |
| CDS Mutation | c.1682C>T |
| AA Mutation | p.Ala561Val(p.A561V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000361675 |
| Start | 134947724:134947724(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1749G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000361675 |
| Start | 134947748:134947748(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs758658636 |
| CDS Mutation | c.1773C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000361675 |
| Start | 134950409:134950409(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs751734611 |
| CDS Mutation | c.1830G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |