Variant #0000000682 (NC_000016.9:g.23646182C>A, NC_000016.9(NM_024675.3):c.1684+1G>T (PALB2))
| Chromosome |
16 |
| Allele |
Unknown |
| Affects function (as reported) |
Probably affects function |
| Affects function (by curator) |
Probably affects function |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.23646182C>A |
| Reference |
- |
| DB-ID |
PALB2_000008 |
| Frequency |
- |
| Average frequency (gnomAD v.2.1.1) |
Retrieve |
| Owner |
Florian Bayersdorfer |
| Database submission license |
Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International |
| Created by |
Florian Bayersdorfer |
| Date created |
2025-10-06 07:51:42 +00:00 (UTC) |
| Date last edited |
N/A |

Variant on transcripts
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