Variant #0000011339 (NC_000005.10:g.112839514T>A, APC(NM_000038.6):c.3920T>A)
| Individual ID |
00004089, 00005037, 00005053, 00005059, 00005123, 00005180, 00005395, 00005477, 00005606, 00005618, 00005621, 00005623, 00005807, 00005830 |
| Chromosome |
5 |
| Allele |
Unknown |
| Affects function (as reported) |
Effect unknown |
| Affects function (by curator) |
Effect unknown |
| DNA change (genomic) (Relative to hg38 / GRCh38) |
g.112839514T>A |
| Reference |
- |
| DB-ID |
APC_000032 See all 20 reported entries |
| dbSNP ID |
- |
| Variant remarks |
- |
| Average frequency (gnomAD v.2.1.1) |
Retrieve |
| Owner |
Pablo Kalfayan-Hospital Italiano |
| Database submission license |
Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International |
| Created by |
Instituto Nacional del Cancer |

Variant on transcripts
Screenings
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