Variant #0000010063 (NC_000016.10:g.3596321C>T, NM_032444.3:c.1756G>A (SLX4))
Individual ID |
00002995 |
Chromosome |
16 |
Allele |
Unknown |
Affects function (as reported) |
Effect unknown |
Affects function (by curator) |
Effect unknown |
DNA change (genomic) (Relative to hg38 / GRCh38) |
g.3596321C>T |
Reference |
- |
DB-ID |
SLX4_000003 |
dbSNP ID |
rs764210911 |
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 |
2024-07-18 14:54:23 -03:00 (-03) |
Date last edited |
N/A |
Variant on transcripts
Screenings
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