Variant #0000000048 (NC_000014.8:g.45658326C>T, NM_020937.2:c.5101C>T (FANCM))
Chromosome |
14 |
Allele |
Unknown |
Affects function (as reported) |
Probably affects function |
Affects function (by curator) |
Probably affects function |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.45658326C>T |
Reference |
- |
DB-ID |
FANCM_000001 |
Frequency |
- |
Average frequency (gnomAD v.2.1.1) |
0.00129 View details |
Owner |
Florian Bayersdorfer |
Database submission license |
Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International |
Created by |
Florian Bayersdorfer |
Date created |
2018-12-07 11:59:46 +00:00 (UTC) |
Date last edited |
N/A |
Variant on transcripts
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