Variant #0000348598 (NC_000016.9:g.23637715G>A, NM_024675.3:c.2590C>T (PALB2))
| Chromosome |
16 |
| Allele |
Unknown |
| Affects function (as reported) |
Probably does not affect function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
likely benign |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.23637715G>A |
| DNA change (hg38) |
g.23626394G>A |
| Published as |
PALB2(NM_024675.3):c.2590C>T (p.P864S, p.(Pro864Ser), p.Pro864Ser), PALB2(NM_024675.4):c.2590C>T (p.P864S) |
| ISCN |
- |
| DB-ID |
PALB2_010114 See all 27 reported entries |
| Variant remarks |
VKGL data sharing initiative Nederland |
| Reference |
- |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
CLASSIFICATION record |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
0.0028 View details |
| Owner |
VKGL-NL_Nijmegen |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Nijmegen |
| Date created |
2018-01-15 20:58:59 +01:00 (CET) |
| Date last edited |
2025-11-01 13:22:20 +01:00 (CET) |

Variant on transcripts
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