Variant #0000009789 (NC_000008.11:g.144516216T>A, NM_004260.4:c.903A>T (RECQL4))
Individual ID |
00002629 |
Chromosome |
8 |
Allele |
Unknown |
Affects function (as reported) |
Effect unknown |
Affects function (by curator) |
Effect unknown |
DNA change (genomic) (Relative to hg38 / GRCh38) |
g.144516216T>A |
Reference |
- |
DB-ID |
RECQL4_000013 |
dbSNP ID |
rs746200109 |
Variant remarks |
- |
Average frequency (gnomAD v.2.1.1) |
Retrieve |
Owner |
Pablo Kalfayan-Hospital Italiano |
Database submission license |
Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International |
Created by |
Instituto Nacional del Cancer |
Date created |
2024-01-17 13:27:17 -02:00 (-02) |
Date last edited |
N/A |
Variant on transcripts
Screenings
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