Variant #0000009169 (NC_000014.9:=, NM_020937.3:c.187G>A (FANCM))
Individual ID |
00001841 |
Chromosome |
14 |
Allele |
Unknown |
Affects function (as reported) |
Effect unknown |
Affects function (by curator) |
Effect unknown |
DNA change (genomic) (Relative to hg38 / GRCh38) |
= |
Reference |
- |
DB-ID |
FANCM_000012 See all 2 reported entries |
dbSNP ID |
- |
Variant remarks |
- |
Average frequency (gnomAD v.2.1.1) |
Genomic location of variant could not be determined |
Owner |
Silvina Sisterna-Hospital de Comunidad |
Database submission license |
Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International |
Created by |
Instituto Nacional del Cancer |
Date created |
2021-11-24 14:09:08 -02:00 (-02) |
Date last edited |
N/A |
Variant on transcripts
Screenings
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