Primary Site >> Stomach Cancer
Gene >> CACNA2D2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000479441 |
| Start | 50381063:50381063(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201610016 |
| CDS Mutation | c.716G>A |
| AA Mutation | p.Arg239His(p.R239H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000479441 |
| Start | 50381006:50381006(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.773G>T |
| AA Mutation | p.Arg258Leu(p.R258L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000479441 |
| Start | 50375675:50375675(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1876A>G |
| AA Mutation | p.Thr626Ala(p.T626A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000479441 |
| Start | 50378920:50378920(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1334A>T |
| AA Mutation | p.Asn445Ile(p.N445I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000479441 |
| Start | 50365856:50365856(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2890G>A |
| AA Mutation | p.Val964Ile(p.V964I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000479441 |
| Start | 50379138:50379138(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1214A>G |
| AA Mutation | p.Asp405Gly(p.D405G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000479441 |
| Start | 50377509:50377509(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs762114746 |
| CDS Mutation | c.1584C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000479441 |
| Start | 50379976:50379976(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.885C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000479441 |
| Start | 50365472:50365472(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3003G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000479441 |
| Start | 50380768:50380768(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs768567846 |
| CDS Mutation | c.822C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000479441 |
| Start | 50367405:50367405(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.2411delC |
| AA Mutation | p.Pro804HisfsTer7(p.P804Hfs*7) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | inframe_deletion |
| Transcription ID | ENST00000479441 |
| Start | 50365085:50365087(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.3217_3219delAAG |
| AA Mutation | p.Lys1073del(p.K1073del) |
| Mutation Classification | In_Frame_Del |
| Feature Type | Transcript |