Variant #0000008628 (NC_000014.9:g.45198718C>T, NM_020937.3:c.5791C>T (FANCM))
Individual ID |
00001521 |
Chromosome |
14 |
Allele |
Unknown |
Affects function (as reported) |
Affects function |
Affects function (by curator) |
Affects function |
DNA change (genomic) (Relative to hg38 / GRCh38) |
g.45198718C>T |
Reference |
- |
DB-ID |
FANCM_000007 See all 2 reported entries |
dbSNP ID |
- |
Variant remarks |
- |
Average frequency (gnomAD v.2.1.1) |
Retrieve |
Owner |
Norma Rossi-Hospital de Córdoba |
Database submission license |
Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International |
Created by |
Instituto Nacional del Cancer |
Date created |
2020-11-07 20:51:09 -02:00 (-02) |
Date last edited |
2023-04-27 16:19:01 -03:00 (-03) |
Variant on transcripts
Screenings
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