Variant #0000009913 (NC_000008.11:g.144516098T>C, NM_004260.4:c.1021A>G (RECQL4))
Individual ID |
00002776 |
Chromosome |
8 |
Allele |
Unknown |
Affects function (as reported) |
Effect unknown |
Affects function (by curator) |
Effect unknown |
DNA change (genomic) (Relative to hg38 / GRCh38) |
g.144516098T>C |
Reference |
- |
DB-ID |
RECQL4_000016 |
dbSNP ID |
rs1022453211 |
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 |
Date created |
2024-03-14 15:06:46 -03:00 (-03) |
Date last edited |
N/A |
Variant on transcripts
Screenings
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