Variant #0000010960 (NC_000014.9:g.45189176G>A, FANCM(NM_020937.4):c.5154G>A)
Individual ID |
00003853 |
Chromosome |
14 |
Allele |
Unknown |
Affects function (as reported) |
Effect unknown |
Affects function (by curator) |
Effect unknown |
DNA change (genomic) (Relative to hg38 / GRCh38) |
g.45189176G>A |
Reference |
- |
DB-ID |
FANCM_000035 |
dbSNP ID |
- |
Variant remarks |
- |
Average frequency (gnomAD v.2.1.1) |
Retrieve |
Owner |
Guillermo Alberto-Instituto Fleming |
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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