Variant #0000657852 (NC_000016.9:g.47683064A>G, NM_000293.2:c.1746A>G (PHKB))
| 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.47683064A>G |
| DNA change (hg38) |
g.47649153A>G |
| Published as |
PHKB(NM_001031835.2):c.1725A>G (p.L575=) |
| ISCN |
- |
| DB-ID |
PHKB_000019 |
| 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) |
0.00015 View details |
| Owner |
VKGL-NL_Rotterdam |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Rotterdam |
| Date created |
2020-03-23 16:13:27 +01:00 (CET) |
| Date last edited |
2020-07-09 16:01:46 +02:00 (CEST) |

Variant on transcripts
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